UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 10-Q

 

(Mark One)

 

x QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the quarterly period ended: March 31,September 30, 2018

 

¨ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the transition period from ____________to _____________

 

Commission File Number: 001-37357

 

INNOVATION PHARMACEUTICALS INC.

(Exact name of registrant as specified in its charter)

(Exact name of registrant as specified in its charter)

Nevada

 

30-0565645

(State or other jurisdiction of

 

(I.R.S. Empl. Ident. No.)

incorporation or organization)

 

Ident. No.)

 

100 CummingsCumming Center, Suite 151-B

Beverly, MA 01915

(Address of principal executive offices, Zip Code)

 

(978)-921-4125

(Registrant’s telephone number, including area code)

(Former Name, Former Address and Former Fiscal Year if Changed Since Last Report)

 

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act during the past 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes x No ¨

 

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes x No ¨

 

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer”, “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

 

Large Accelerated Filer

¨

Accelerated Filer

x

Non-Accelerated Filer

¨

Smaller reporting company

¨x

 (Do not check if a smaller reporting company)

 

Emerging growth company

¨

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. o¨

 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes.Yes ¨ No x

 

The number of shares outstanding of each of the issuer’s classes of common equity, as of May 6,November 2, 2018 is as follows:

 

Class of Securities

 

Shares Outstanding

Common Stock Class A, $0.0001 par value

 

155,091,427163,676,190

Common Stock Class B, $0.0001 par value

 

None

 

 
 
 
 

 

INNOVATION PHARMACEUTICALS INC.

FORM 10-Q

For the Quarter Ended March 31,September 30, 2018

 

TABLE OF CONTENTS

 

PART I – FINANCIAL INFORMATION

 

Item 1.

Financial Statements

 

4

 

 

Condensed Balance Sheets as of March 31,September 30, 2018 (unaudited) and June 30, 20172018 (audited)

 

4

 

 

Condensed Statements of Operations (unaudited) for the three months and nine months ended March 31,September 30, 2018 and 2017 (unaudited)

 

5

 

 

Condensed Statements of Cash Flows (unaudited) for the ninethree months ended March 31,September 30, 2018 and 2017 (unaudited)

 

6

 

 

Notes to Condensed Financial Statements (unaudited)

 

7

 

Item 2.

Management’s Discussion and Analysis of Financial Condition and Results of Operations

 

2019

 

Item 3.

Quantitative and Qualitative Disclosures About Market Risk

 

3228

 

Item 4.

Controls and Procedures

 

3228

 

 

PART II – OTHER INFORMATION

 

Item 1.

Legal Proceedings

 

3329

 

Item 1A

Risk Factors

 

3329

 

Item 2.

Unregistered Sales of Equity Securities and Use of Proceeds

 

3329

 

Item 3.

Defaults Upon Senior Securities

 

3329

 

Item 4.

Mine Safety Disclosures

 

3329

 

Item 5.

Other Information

 

3329

 

Item 6.

Exhibits

 

3330

 

 

 

 

SIGNATURES

 

3531

 

 
2
 
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FORWARD-LOOKING STATEMENTS

 

This report contains forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended. Any statements contained in this report that are not statements of historical fact may be forward-looking statements. When we use the words “intends,” “estimates,” “predicts,” “potential,” “continues,” “anticipates,” “plans,” “expects,” “believes,” “should,” “could,” “may,” “will” or the negative of these terms or other comparable terminology, we are identifying forward-looking statements. These forward-looking statements include, but are not limited to, statements concerning our future drug development plans and projected timelines for the initiation and completion of preclinical and clinical trials; statements relating to potential licensing, partnering or similar arrangements concerning our drug compounds; the potential for the results of ongoing preclinical or clinical trials; other statements regarding our future product development and regulatory strategies, including with respect to specific indications; any statements regarding our future financial performance, results of operations expenditures or sufficiency of capital resources to fund our operating requirements; and any other statements which are other than statements of historical fact. Forward-looking statements involve risks and uncertainties, which may cause our actual results, performance or achievements to be materially different from those expressed or implied by forward-looking statements. These factors include, but are not limited to, our ability to continue as a going concern and our capital needs; our ability to continue to fund and successfully progress internal research and development efforts and to create effective, commercially-viable drugs; our ability to effectively and timely conduct clinical trials; and our ability to ultimately distribute our drug candidates; compliance with regulatory requirements; and our capital needs,requirements, as well as other factors described elsewhere in this report and our other reports filed with the Securities and Exchange Commission (the “SEC”). Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity, performance or achievements.

 

Forward-looking statements speak only as of the date on which they are made. Except as may be required by applicable law, we do not undertake or intend to update or revise our forward-looking statements, and we assume no obligation to update any forward-looking statements contained in this report as a result of new information or future events or developments. Thus, you should not assume that our silence over time means that actual events are bearing out as expressed or implied in such forward-looking statements. You should carefully review and consider the various disclosures we make in this report and our other reports filed with the SEC that attempt to advise interested parties of the risks, uncertainties and other factors that may affect our business. Readers are cautioned not to put undue reliance on forward-looking statements.

 

For further information about these and other risks, uncertainties and factors, please review the disclosure included in our Annual Report on Form 10-K under “Part I, Item 1A, Risk Factors” and in this report under “Part II, Item 1A, Risk Factors.”

 

 
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PART I. FINANCIAL INFORMATION

 

ITEM 1. FINANCIAL STATEMENTS

 

INNOVATION PHARMACEUTICALS INC.

CONDENSED BALANCE SHEETS

(Rounded to nearest thousand except for shares data)

 

 

March 31,

 

June 30,

 

 

September 30,

 

June 30,

 

 

2018

 

 

2017

 

 

2018

 

 

2018

 

(Unaudited)

 

 

 

 

(Unaudited)

 

 

ASSETS

ASSETS

ASSETS

Current Assets:

 

 

 

 

 

 

 

 

 

 

Cash

 

$1,336,000

 

$4,141,000

 

 

$306,000

 

$2,424,000

 

Prepaid expenses

 

40,000

 

308,000

 

Prepaid expenses and other current assets

 

55,000

 

98,000

 

Security deposits

 

78,000

 

-

 

 

 

-

 

 

 

78,000

 

Subscription receivable

 

 

-

 

 

 

26,000

 

Total Current Assets

 

 

1,454,000

 

 

 

4,475,000

 

 

 

361,000

 

 

 

2,600,000

 

 

 

 

 

 

Other Assets:

 

 

 

 

 

 

 

 

 

 

Patents - net

 

4,032,000

 

4,212,000

 

Equipment - net

 

93,000

 

120,000

 

Patents – net

 

3,705,000

 

3,780,000

 

Equipment – net

 

2,000

 

2,000

 

Deferred offering costs - net

 

173,000

 

227,000

 

 

159,000

 

159,000

 

Security deposits

 

 

-

 

 

 

78,000

 

 

 

78,000

 

 

 

-

 

Total Other Assets

 

 

4,298,000

 

 

 

4,637,000

 

 

 

3,944,000

 

 

 

3,941,000

 

Total Assets

 

$5,752,000

 

 

$9,112,000

 

 

$4,305,000

 

 

$6,541,000

 

 

 

 

 

 

 

 

 

 

 

LIABILITIES AND STOCKHOLDERS' DEFICIENCY

LIABILITIES AND STOCKHOLDERS' DEFICIENCY

LIABILITIES AND STOCKHOLDERS' DEFICIENCY

Current Liabilities:

 

 

 

 

 

 

 

 

 

 

Accounts payable - (including related party payables of approximately $1,486,000 and 1,506,000, respectively)

 

$4,122,000

 

$4,699,000

 

Accrued expenses - (including related party accruals of approximately $25,000 and $38,000, respectively)

 

306,000

 

711,000

 

Accrued salaries and payroll taxes - (including related party accrued salaries of approximately $2,953,000 and $2,953,000, respectively)

 

3,017,000

 

3,144,000

 

Accounts payable - (including related party payables of approximately $1,504,000 and 1,504,000, respectively)

 

$2,790,000

 

$3,185,000

 

Accrued expenses - (including related party accruals of approximately $44,000 and $58,000, respectively)

 

174,000

 

266,000

 

Accrued salaries and payroll taxes - (including related party accrued salaries of approximately $3,129,000 and $2,953,000, respectively)

 

3,291,000

 

3,219,000

 

Convertible note payable - related party

 

 

2,022,000

 

 

 

2,022,000

 

 

 

2,022,000

 

 

 

2,022,000

 

Total Current Liabilities

 

 

9,467,000

 

 

 

10,576,000

 

 

 

8,277,000

 

 

 

8,692,000

 

Total Liabilities

 

 

9,467,000

 

 

 

10,576,000

 

 

 

8,277,000

 

 

 

8,692,000

 

 

 

 

 

 

 

 

 

 

 

Commitments and contingencies (Note 7)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Stockholders’ Deficiency

 

 

 

 

 

 

 

 

 

 

Preferred stock, $0.001 par value, 10,000,000 designated shares, no shares issued and outstanding

 

-

 

-

 

 

-

 

-

 

Common Stock - Class A, $0.0001 par value, 300,000,000 shares authorized, 147,091,427 and 135,536,501 issued as of March 31, 2018 and June 30, 2017, respectively, 147,091,427 and 135,274,421 outstanding as of March 31, 2018 and June 30, 2017, respectively

 

15,000

 

14,000

 

Common Stock - Class B, (10 votes per share); $0.0001 par value, 100,000,000 shares authorized, no shares issued and outstanding as of March 31, 2018 and June 30, 2017, respectively

 

-

 

-

 

Common Stock - Class A, $0.0001 par value, 300,000,000 shares authorized, 163,676,190 shares and 163,103,927 shares issued and outstanding as of September 30, 2018 and June 30, 2018, respectively

 

17,000

 

17,000

 

Common Stock - Class B, (10 votes per share); $0.0001 par value, 100,000,000 shares authorized, no shares issued and outstanding as of September 30, 2018 and June 30, 2018

 

-

 

-

 

Additional paid-in capital

 

77,324,000

 

68,295,000

 

 

83,976,000

 

83,747,000

 

Accumulated deficit

 

(81,054,000)

 

(69,553,000)

 

 

(87,965,000)

 

 

(85,915,000)

Treasury Stock, at cost (0 shares and 262,080 shares as of March 31, 2018 and June 30, 2017, respectively)

 

 

-

 

 

 

(220,000)

Total Stockholders’ Deficiency

 

 

(3,715,000)

 

 

(1,464,000)

 

 

(3,972,000)

 

 

(2,151,000)

Total Liabilities and Stockholders’ Deficiency

 

$5,752,000

 

 

$9,112,000

 

 

$4,305,000

 

 

$6,541,000

 

 

The accompanying notes are an integral part of these condensed financial statements

 

 
4
 
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INNOVATION PHARMACEUTICALS INC.

CONDENSED STATEMENTS OF OPERATIONS

FOR THE THREE MONTHS AND NINE MONTHS ENDED MARCH 31SEPTEMBER 30, 2018 AND 2017

(Unaudited)

(Rounded to nearest thousand except for shares and per share data)

 

 

For the Three Months

Ended

 

For the Nine Months

Ended

 

 

March 31,

 

March 31,

 

 

2018

 

 

2017

 

 

2018

 

 

2017

 

 

2018

 

 

2017

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Revenues

 

$-

 

 

$-

 

 

$-

 

 

$-

 

 

$-

 

 

$-

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Research and development expenses

 

1,776,000

 

3,182,000

 

9,544,000

 

8,142,000

 

 

1,357,000

 

3,805,000

 

General and administrative expenses

 

295,000

 

331,000

 

889,000

 

1,037,000

 

 

260,000

 

297,000

 

Officers' payroll and payroll tax expenses

 

132,000

 

138,000

 

392,000

 

398,000

 

 

123,000

 

130,000

 

Professional fees

 

 

195,000

 

 

 

201,000

 

 

 

525,000

 

 

 

562,000

 

 

 

259,000

 

 

 

252,000

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Total operating expenses

 

 

2,398,000

 

 

 

3,852,000

 

 

 

11,350,000

 

 

 

10,139,000

 

 

 

1,999,000

 

 

 

4,484,000

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Loss from operations

 

 

(2,398,000)

 

 

(3,852,000)

 

 

(11,350,000)

 

 

(10,139,000)

 

 

(1,999,000)

 

 

(4,484,000)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Other income (expenses)

 

 

 

 

 

 

 

 

 

Other income (expense)

 

 

 

 

 

Interest income

 

-

 

-

 

1,000

 

2,000

 

 

-

 

1,000

 

Interest expense

 

 

(51,000)

 

 

(51,000)

 

 

(152,000)

 

 

(152,000)

 

 

(51,000)

 

 

(51,000)

Total other income - net

 

 

(51,000)

 

 

(51,000)

 

 

(151,000)

 

 

(150,000)

 

 

 

 

 

 

Total other expense - net

 

 

(51,000)

 

 

(50,000)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Loss before provision for income taxes

 

(2,449,000)

 

(3,903,000)

 

(11,501,000)

 

(10,289,000)

 

(2,050,000)

 

(4,534,000)

Provision for income taxes

 

 

-

 

 

 

-

 

 

 

-

 

 

 

-

 

 

 

-

 

 

 

-

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss

 

$(2,449,000)

 

$(3,903,000)

 

$(11,501,000)

 

$(10,289,000)

 

$(2,050,000)

 

$(4,534,000)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Basic and diluted loss per share

 

$(0.02)

 

$(0.03)

 

$(0.08)

 

$(0.08)

Basic and diluted loss per share attributable to common stockholders

 

$(0.01)

 

$(0.03)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Weighted average number of common shares outstanding

 

 

146,071,627

 

 

 

127,270,598

 

 

 

141,296,395

 

 

 

125,599,470

 

Weighted average number of common shares

 

 

163,284,314

 

 

 

137,171,811

 

 

The accompanying notes are an integral part of these condensed financial statements.

 

 
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INNOVATION PHARMACEUTICALS INC.

CONDENSED STATEMENTS OF CASH FLOWFLOWS

FOR THE NINETHREE MONTHS ENDED MARCH 31,SEPTEMBER 30, 2018 AND 2017

(Unaudited)

(Rounded to nearest thousand)

 

 

2018

 

 

2017

 

 

 

 

 

 

 

2018

 

 

2017

 

CASH FLOWS FROM OPERATING ACTIVITIES:

 

 

 

 

 

 

 

 

 

 

Net loss

 

$(11,501,000)

 

$(10,289,000)

 

$(2,050,000)

 

$(4,534,000)

Adjustments to reconcile net loss to net cash used in operating activities:

 

 

 

 

 

 

 

 

 

 

Common stock and stock options issued as payment for compensation, services rendered and financing costs

 

1,665,000

 

1,026,000

 

Common stock and stock options issued as employee compensation and payment for services rendered and financing costs

 

229,000

 

369,000

 

Amortization of patent costs

 

289,000

 

277,000

 

 

94,000

 

96,000

 

Depreciation of equipment

 

28,000

 

24,000

 

 

-

 

9,000

 

Changes in operating assets and liabilities:

 

 

 

 

 

 

 

 

 

 

Prepaid expenses and security deposits

 

268,000

 

165,000

 

 

43,000

 

121,000

 

Accounts payable

 

(578,000)

 

664,000

 

 

(395,000)

 

711,000

 

Accrued expenses

 

(406,000)

 

130,000

 

 

(92,000)

 

(355,000)

Accrued officers' salaries and payroll taxes

 

 

(127,000)

 

 

54,000

 

 

 

72,000

 

 

 

(106,000)

 

 

 

 

 

 

 

 

 

 

Net cash used in operating activities

 

 

(10,362,000)

 

 

(7,949,000)

 

 

(2,099,000)

 

 

(3,689,000)

 

 

 

 

 

 

 

 

 

 

CASH FLOWS FROM INVESTING ACTIVITIES:

 

 

 

 

 

 

 

 

 

 

Additions to property, plant and equipment

 

-

 

(63,000)

Patent costs

 

 

(108,000)

 

 

(256,000)

 

 

(19,000)

 

 

(22,000)

 

 

 

 

 

 

 

 

 

 

Net cash used in investing activities

 

 

(108,000)

 

 

(319,000)

 

 

(19,000)

 

 

(22,000)

 

 

 

 

 

 

 

 

 

 

CASH FLOWS FROM FINANCING ACTIVITIES:

 

 

 

 

 

 

 

 

 

 

Sales of common stock, net of offering costs

 

7,837,000

 

7,571,000

 

 

-

 

2,508,000

 

Purchase of treasury stock

 

 

(172,000)

 

 

-

 

 

 

-

 

 

 

(5,000)

 

 

 

 

 

 

 

 

 

 

Net cash provided by financing activities

 

 

7,665,000

 

 

 

7,571,000

 

 

 

-

 

 

 

2,503,000

 

 

 

 

 

 

 

 

 

 

 

NET DECREASE IN CASH

 

(2,805,000)

 

(697,000)

 

(2,118,000)

 

(1,208,000)

 

 

 

 

 

 

 

 

 

 

CASH, BEGINNING OF PERIOD

 

 

4,141,000

 

 

 

6,310,000

 

 

 

2,424,000

 

 

 

4,141,000

 

 

 

 

 

 

 

 

 

 

 

CASH, END OF PERIOD

 

$1,336,000

 

 

$5,613,000

 

 

$306,000

 

 

$2,933,000

 

 

 

 

 

 

 

 

 

 

 

SUPPLEMENTAL DISCLOSURES OF CASH FLOW INFORMATION

 

 

 

 

 

 

 

 

 

 

Cash paid for interest

 

$156,000

 

 

$44,000

 

 

$63,000

 

 

$32,000

 

 

 

 

 

 

 

 

 

 

 

SUPPLEMENTAL DISCLOSURE OF NON-CASH FLOW

 

 

 

 

 

INVESTING AND FINANCING ACTIVITIES

 

 

 

 

 

SUPPLEMENTAL DISCLOSURE OF NON-CASH FLOW INVESTING AND FINANCING ACTIVITIES

 

 

 

 

 

Commitment shares issued as deferred offering costs

 

$215,000

 

 

$-

 

 

$-

 

 

$215,000

 

Reversal of subscription receivable to treasury stock

 

$26,000

 

 

$-

 

 

$-

 

 

 

26,000

 

 

The accompanying notes are an integral part of these condensed financial statements.

 

 
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INNOVATION PHARMACEUTICALS INC.

NOTES TO CONDENSED FINANCIAL STATEMENTS

MARCH 31SEPTEMBER 30, 2018

 (Unaudited)

 

Note 1. Basis of Presentation and Nature of Operations

 

Unaudited Interim Financial Information

 

The accompanying unaudited condensed financial statements of Innovation Pharmaceuticals Inc. have been prepared in accordance with the rules and regulations of the Securities and Exchange Commission, or the SEC, including the instructions to Form 10-Q and Regulation S-X. Certain information and note disclosures normally included in financial statements prepared in accordance with generally accepted accounting principles in the United States of America (“U.S. GAAP”) have been condensed or omitted from these statements pursuant to such rules and regulations and, accordingly, they do not include all the information and notes necessary for comprehensive financial statements and should be read in conjunction with our audited financial statements for the year ended June 30, 2017,2018, included in our Annual Report on Form 10-K for the year ended June 30, 2017.2018.

 

In the opinion of the management of Innovation Pharmaceuticals Inc., all adjustments, which are of a normal recurring nature, necessary for a fair statement of the results for the three-month and nine-monththree month periods have been made. Results for the interim periodsperiod presented are not necessarily indicative of the results that might be expected for the entire fiscal year. When used in these notes, the terms “Company”, “we”, “us” or “our” mean Innovation Pharmaceuticals Inc.

 

Basis of Presentation and Name Change

 

Innovation Pharmaceuticals Inc. (the “Company”) was incorporated on August 1, 2005 in the State of Nevada. Effective June 5, 2017, the Company amended its Articles of Incorporation and changed its name from Cellceutix Corporation to Innovation Pharmaceuticals Inc. In accordance with Section 92A.180 of the Nevada Revised Statutes, stockholder approval of the name change was not required.

 

The Company is a clinical stage biopharmaceutical company and has no customers, products or revenues to date. The Company’s common stock is quoted on OTCQB, symbol “IPIX”.

 

Nature of Operations - Overview

 

We are in the business of developing innovative small molecule therapies to treat diseases with significant medical need, particularly in the areas of inflammatory diseases, cancer, dermatology and anti-infectives. Our strategy is to use our business and scientific expertise to maximize the value of our pipeline. We will do this by focusing initially on our lead compounds, Brilacidin, Kevetrin and Prurisol and advancing them as quickly as possible along the regulatory pathway. We will develop the highest quality data and broadest intellectual property to support our compounds.

 

We currently own all development and marketing rights to our products. In order to successfully develop and market our products, we may have to partner with other companies. Prospective partners may require that we grant them significant development and/or commercialization rights in return for agreeing to share the risk of development and/or commercialization.

 

Note 2. Going Concern and Liquidity

 

As of June 30, 2017,These financial statements have been prepared on the assumption that the Company adopted Accounting Standards Codification 205-40. This guidance amended the existing requirements for disclosing information about an entity’s ability to continue asis a going concern, which contemplates the realization of its assets and explicitly requires management to assess an entity’s ability to continue as a going concern and to provide related disclosurethe settlement of its liabilities in certain circumstances. This guidance was effective for annual reporting periods ending after December 15, 2016, and for annual and interim reporting periods thereafter. The following information reflects the resultsnormal course of management’s assessment, plans and conclusion of the Company’s ability to continue as a going concern.

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operations.

 

We have incurred recurring losses since inception and expect to continue to incur losses as a result of costs and expenses related to our research and continued development of our compounds and our corporate general and administrative expenses. As of March 31,September 30, 2018, the Company has an accumulated deficit of approximately $81.1$88.0 million, representative of recurring losses since inception. The Company is a development stage pharmaceutical company that has no sales as it does not have any products in the market and will continue to not have any revenues until it begins to market its products after it has obtained the necessary Federal Drug Administration (the “FDA”) approval. As a result, the Company expects to continue to incur losses over the next 12 months from the date of this filing. Accordingly, the Company’s planned operations, including total budgeted expenditures of approximately $14 million for the next twelve months, raise substantial doubt about its ability to continue as a going concern.

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At March 31,September 30, 2018, the Company’s cash amounted to $1.3$0.3 million and current liabilities amounted to $9.5$8.3 million, of which $6.5$6.7 million were payables to related parties with no immediate payment terms (See Note 8- Related Party TransactionsTransactions). Subsequent to September 30, 2018, in October 2018, aggregate gross proceeds of approximately $2.0 million were raised through the Notes to Condensed Financial Statements sectionsale of convertible preferred stock (see below). The Company had expended substantial funds on its clinical trials and expects to continue our spending on research and development expenditures. The Company’s net cash used in operating activities for the ninethree months ended March 31,September 30, 2018 was approximately $10.4$2.1 million, and current projections indicate that the Company will have continued negative cash flows from operating activities for the foreseeable future. Our net losses incurred for the ninethree months ended March 31,September 30, 2018 and 2017, amounted to $11.5$2.1 million and $10.3$4.5 million, respectively, and we had a working capital deficit of approximately $8.0$7.9 million and $6.1 million, respectively at March 31,September 30, 2018 and June 30, 2017.2018.

 

Accordingly,The Company's primary sources of liquidity are cash and cash equivalents as well as issuances of its equity securities. The Company is party to a common stock purchase agreement (the “Purchase Agreement”) with Aspire Capital Fund, LLC (“Aspire Capital”) that provides that, upon the terms and subject to the conditions and limitations set forth therein, Aspire Capital is committed to purchase up to an aggregate of $30.0 million of the Company's common stock over the 36-month term of the Purchase Agreement. As of September 30, 2018, the available balance under the Purchase Agreement is approximately $22.3 million. However, as of date of this report, the conditions for sales under the Purchase Agreement are not satisfied and no sales may occur thereunder. In particular, the Purchase Agreement provides that the Company and Aspire Capital will not affect any sales under the Purchase Agreement when the closing sales price of the Company’s planned operations, including total budgeted expenditures of approximately $12.2 millioncommon stock is less than $0.25 per share. Recently, the Company’s common stock has traded below $0.25 per share, and there is substantial uncertainty regarding the Company’s continued ability to sell shares under the Purchase Agreement in order to meet the Company's projected working capital requirements for the next twelve12 months raise doubt aboutfrom the date of the issuance of the financial statements (or available to be issued).

After the date of the financial statements, on October 5, 2018, the Company entered into a securities purchase agreement with one multi-family office for the sale of an aggregate of 2,000 shares of the Company’s newly-created Series B 5% convertible preferred stock for aggregate gross proceeds of approximately $2.0 million. Under the securities purchase agreement, the Company issued to the investors warrants to purchase up to an additional 8,000 shares of preferred stock. As the Company cannot be certain the remaining warrants will be exercised, there can be no assurance those funds will be available when needed.

The Company expects to seek to obtain additional funding through business development activities (i.e. licensing and partnerships) and future equity issuances. There can be no assurance as to the availability or terms upon which such financing and capital might be available. The Company will be unable to proceed with its abilityplanned drug development programs, meet its administrative expense requirements, capital costs, or staffing costs without additional financing from Aspire Capital, the multi-family office or another source of capital. These financial statements do not include any adjustments related to the carrying values and classifications of assets and liabilities that would be necessary should the Company be unable to continue as a going concern. The Company’s plans to alleviate the doubt of its ability to continue as a going concern primarily include controlling the timing and spending on its research and development programs, thereby being able to decrease its current budgeted expenditures mentioned above for the next 12 months, as needed and to continue raising additional funds through equity financings from its common stock purchase agreement with Aspire Capital Fund, LLC, an Illinois limited liability company (“Aspire Capital”). The Company may consider other plans to fund operations including: (1) raising additional capital through debt financings or from other sources; (2) additional funding through new relationships to help fund future clinical trial costs (i.e. licensing and partnerships); (3) reducing spending on one or more research and development programs by discontinuing development; and/or (4) restructuring operations to change its overhead structure. The Company may issue securities, including shares of common stock, shares of preferred stock and stock purchase contracts through private placement transactions or registered public offerings, pursuant to its registration statement on Form S-3 filed with the SEC on September 11, 2017 and declared effective on September 21, 2017. Pursuant to the instructions to Form S-3, if the Company’s non-affiliate market capitalization as of an applicable measurement time, such as upon the filing of the Company’s Annual Report on Form 10-K, does not equal or exceed $75 million, the Company will be unable to offer and sell securities from its effective shelf registration statement on Form S-3.

 

The Company’s future liquidity needs, and ability to address those needs, will largely be determined by the success of its product candidates and key development and regulatory events and its decisions in the future.

The Company believes that the actions discussed above are probable of occurring and alleviating the substantial doubt raised by our historical operating results and satisfying our estimated liquidity needs twelve months from the issuance of the accompanying financial statements.

On September 6, 2017, the Company entered into a new $30 million common stock purchase agreement with Aspire Capital (the “2017 Agreement”) to replace the prior 2015 $30 million common stock purchase agreement with Aspire Capital (the “2015 Agreement”). During the period from July 1, 2017 to September 5, 2017, the Company generated proceeds of approximately $2.1 million under the 2015 Agreement from the sale of approximately 2.6 million shares of its common stock. During the period from September 6, 2017 to March 31, 2018, the Company generated proceeds of approximately $5.7 million under the 2017 Agreement from the sale of approximately 8.7 million shares of its common stock. As of March 31, 2018, the available balance under the 2017 Agreement is approximately $24.3 million.

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Note 3. Significant Accounting Policies and Recent Accounting Pronouncements

 

Use of Estimates

 

The preparation of financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect certain reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date of the financial statements, and the reported amounts of revenues and expenses during the reporting periods. Significant items subject to such estimates and assumptions include contract research accruals, recoverability of long-lived assets, measurementvaluation of stock-based compensation,equity grants and the periods of performance under collaborative research and development agreements.income tax valuation. The Company bases its estimates on historical experience and various other assumptions that management believes to be reasonable under the circumstances. Changes in estimates are recorded in the period in which they become known. Actual results could differ from those estimates.

 

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NetBasic Loss Perper Share

 

Basic and diluted loss per share is computed based on the weighted-average common shares and common share equivalents outstanding during the period. Common share equivalents consist of stock options, convertible notes payable underlying shares and unvested restricted stock. Common share equivalents of 47 million56,271,542 and 46 million47,242,085 shares of common stock were excluded from the computation of diluted loss per share for the ninethree months ended March 31,September 30, 2018 and 2017, respectively, because we incurred net losses for the ninethree months ended March 31,September 30, 2018 and 2017, and the effect of including these potential common shares in the net loss per share calculations would be anti-dilutive and are therefore not included in the calculations.

 

Treasury Stock

The Company accounts for treasury stock using the cost method. There were 0 shares and 262,080 shares of treasury stock outstanding, purchased at a total cumulative cost of $0 and $220,000 at March 31, 2018 and June 30, 2017, respectively (see Note 10).

Treasury stock, representing shares of the Company’s common stock that have been acquired for payroll tax withholding on vested stock grants, is recorded at its acquisition cost and these shares are not considered outstanding.

Accounting for Stock Based Compensation

 

The stock-based compensation expense incurred by the Company for employees and directors in connection with its stock option plan is based on the employee model of ASC 718, and the fair market value of the options is measured at the grant date. Under ASC 718 an employee is defined as “An individual over whom the grantor of a share-based compensation award exercises or has the right to exercise sufficient control to establish an employer-employee relationship based on common law as illustrated in case law and currently under U.S. tax“tax regulations”. Our consultants do not meet the employer-employee relationship as defined by the IRS and therefore are accounted for under ASC 505-50.

 

ASC 505-50-30-11 further provides that an issuer shall measure the fair value of the equity instruments in these transactions using the stock price and other measurement assumptions as of the earlier of the following dates, referred to as the measurement date:

 

 

i.

The date at which a commitment for performance by the counterparty to earn the equity instruments is reached (a performance commitment); and

 

ii.

The date at which the counterparty’s performance is complete.

 

We have elected to use the Black-Scholes-Merton pricing model to determine the fair value of stock options on the dates of grant. Restricted stock isunits are measured based on the fair market values of the underlying stock on the dates of grant. We recognize stock-based compensation using the straight-line vesting method overmethod.

The components of stock-based compensation expense included in the requisite service periodCompany’s Condensed Statement of Operations for the equity awards.three months ended September 30, 2018 and 2017 are as follows (rounded to nearest thousand):

 

 

Three months ended
September 30

 

 

 

2018

 

 

2017

 

Research and development expenses

 

 

 

 

 

 

Professional fees

 

$13,000

 

 

$-

 

Employees’ bonus

 

 

44,000

 

 

 

32,000

 

Officers’ bonus

 

 

172,000

 

 

 

337,000

 

Total stock-based compensation expense

 

$229,000

 

 

$369,000

 

 

 
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The components of stock-based compensation expense included in the Company’s Condensed Statements of Operations for the three months and nine months ended March 31, 2018 and 2017 are as follows (rounded to nearest thousand):

 

 

Three months ended

March 31

 

 

Nine months ended

March 31

 

 

 

2018

 

 

2017

 

 

2018

 

 

2017

 

Research and development expenses

 

 

 

 

 

 

 

 

 

 

 

 

Professional fees

 

$80,000

 

 

$5,000

 

 

$80,000

 

 

$55,000

 

Employees’ bonus

 

 

41,000

 

 

 

48,000

 

 

 

115,000

 

 

 

110,000

 

Officers’ bonus

 

 

144,000

 

 

 

283,000

 

 

 

1,470,000

 

 

 

861,000

 

Total stock-based compensation expense

 

$265,000

 

 

$336,000

 

 

$1,665,000

 

 

$1,026,000

 

Recent Adopted Accounting Pronouncements

 

Stock Compensation -In March 2016,July 2017, the FASB issued ASU 2016-09, Compensation – Stock Compensation2017-11, Earnings Per Share (Topic 718)260), Distinguishing Liabilities from Equity (Topic 480) and Derivatives and Hedging (Topic 815): Improvements to Employee Share-Based PaymentI. Accounting which simplifiedfor Certain Financial Instruments with Down Round Features; and II. Replacement of the income tax consequences,Indefinite Deferral for Mandatorily Redeemable Financial Instruments of Certain Nonpublic Entities and Certain Mandatorily Redeemable Non-controlling Interests with a Scope Exception. Part I of this update addresses the complexity of accounting for forfeitures and classificationcertain financial instruments with down round features. Down round features are features of certain equity-linked instruments (or embedded features) that result in the strike price being reduced on the Statementbasis of Cash Flowsthe pricing of future equity offerings. Current accounting guidance creates cost and complexity for entities that issue financial instruments (such as warrants and convertible instruments) with (i) excess tax benefits being classified as cash inflows provided by operating activities,down round features that require fair value measurement of the entire instrument or conversion option. Part II of this update addresses the difficulty of navigating Topic 480, Distinguishing Liabilities from Equity, because of the existence of extensive pending content in the FASB Accounting Standards Codification. This pending content is the result of the indefinite deferral of accounting requirements about mandatorily redeemable financial instruments of certain nonpublic entities and (ii) cash paid to taxing authorities arising from the withholdingcertain mandatorily redeemable non-controlling interests. The amendments in Part II of shares from employees being classified as cash outflows used in financing activities.this update do not have an accounting effect. This standardASU is effective for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2016,2018, with early adoption permitted. The adoption of ASU 2017-11, during the year ended June 30, 2018, did not have any impact on the financial statements and related disclosures.

In May 2017, the FASB issued ASU 2017-09, Compensation-Stock Compensation (Topic 718): Scope of Modification Accounting. ASU 2017-09 provides clarity and reduces both (1) diversity in practice and (2) cost and complexity when applying the guidance in Topic 718, to a change to the terms or conditions of a share-based payment award. The amendments in ASU 2017-09 should be applied prospectively to an award modified on or after the adoption date. This ASU is effective for fiscal years, and interim periods within those years, beginning after December 15, 2017. This new pronouncement washas been adopted on July 1, 2016in the fourth quarter of fiscal 2018 and did not have a material effect on the Company’s financial position, or results of operations but had an effect of the classification ofor cash paid to taxing authorities arising from the withholding of shares from employees (treasury stock), classified as cash outflows used in financing activities.

In June 2014, the FASB issued ASU 2014-12, “Compensation—Stock Compensation.” The amendments in this ASU apply to reporting entities that grant their employees share-based payments in which the terms of the award provide that a performance target can be achieved after the requisite service period. This ASU is the final version of Proposed ASU EITF-13D, “Compensation—Stock Compensation (Topic 718): Accounting for Share-Based Payments When the Terms of an Award Provide That a Performance Target Could Be Achieved after the Requisite Service Period,” which has been deleted. The amendments require that a performance target that affects vesting and that could be achieved after the requisite service period be treated as a performance condition. A reporting entity should apply existing guidance in Topic 718 as it relates to awards with performance conditions that affect vesting to account for such awards. As such, the performance target should not be reflected in estimating the grant-date fair value of the award. Compensation cost should be recognized in the period in which it becomes probable that the performance target will be achieved and should represent the compensation cost attributable to the period(s) for which the requisite service has already been rendered. If the performance target becomes probable of being achieved before the end of the requisite service period, the remaining unrecognized compensation cost should be recognized prospectively over the remaining requisite service period. The total amount of compensation cost recognized during and after the requisite service period should reflect the number of awards that are expected to vest and should be adjusted to reflect those awards that ultimately vest. The requisite service period ends when the employee can cease rendering service and still be eligible to vest in the award if the performance target is achieved. As indicated in the definition of vest, the stated vesting period (which includes the period in which the performance target could be achieved) may differ from the requisite service period. The amendments in this ASU are effective for annual periods and interim periods within those annual periods beginning after December 15, 2015. The implementation of this standard did not have a material impact on the Company’s accompanying condensed financial statements.flows.

 

Recently Issued Accounting Guidance

 

In May 2014, the FASB issued authoritative guidance that defines how companies should report revenues from contracts with customers. The standard requires an entity to recognize revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services. It provides companies with a five-step, principles-based model to use in accounting for revenue and supersedes current revenue recognition requirements, including most industry-specific and transaction-specific revenue guidance. In August 2015, the FASB deferred the effective date of the new revenue standard by one year. As a result, the new standard would not be effective for the Company until 2019. In addition, the FASB is allowing companies to early adopt this guidance for non-public entities beginning in fiscal year 2017. The guidance permits an entity to apply the standard retrospectively to all prior periods presented, with certain practical expedients, or apply the requirements in the year of adoption, through a cumulative adjustment. The Company will apply this new guidance when it becomes effective and has not yet selected a transition method. The Company, due to not having any revenue currently and in the foreseeable future, has concluded that the impact of the adoption of this accounting standard on its financial statements will not be material.

 

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In February 2016,June 2018, the FASB issued ASU No. 2016-02, “Leases2018-07, Compensation – Stock Compensation (Topic 842)”.718): Improvements to Nonemployee Share-Based Payment Accounting, which allows companies to account for nonemployee awards in the same manner as employee awards. The guidance requires that a lessee recognize in the statement of financial position a liability to make lease payments (the lease liability) and a right of use asset representing its right to use the underlying asset for the lease term. The guidance requires the following for finance leases: the right-of-use asset and a lease liability will be initially measured at the present value of the lease payments, in the statement of financial position; interest on the lease liability will be recognized separately from amortization of the right-of-use asset in the statement of comprehensive income; and repayments of the principal portion of the lease liability will be classified within financing activities and payments of interest on the lease liability and variable lease payments within operating activities in the statement of cash flows. The guidance requires the following for operating leases: the right-of-use asset and a lease liability will be initially measured at the present value of the lease payments, in the statement of financial position; a single lease cost will be recognized, calculated so that the cost of the lease is allocated over the lease term on a generally straight-line basis; and all cash payments will be classified within operating activities in the statement of cash flows. Under Topic 842 the accounting applied by a lessor is largely unchanged from that applied under previous U.S. GAAP. The amendments in Topic 842 are effective for fiscal years beginning after December 15, 2018, includingand interim periods within those fiscal years. Management has determined that based on current accounting and lease contract information theannual periods. The adoption of ASU No. 2016-02 is2018-07 will not expected to have a significantmaterial impact on the Company’s financial position, results of operations and disclosures. However, management is continually evaluating the future impact of ASU No. 2016-02 based on changes in the Company’s financial statements through the period of adoption.statements.

 

Intangibles, Goodwill and Other —In January 2017,In February 2016, the FASB issued ASUAccounting Standards Update ("ASU") No. 2017-04, “Intangibles – Goodwill2016-02 (Topic 842) Leases, which requires lessees to recognize a right-of-use asset and Other (Topic 350) – Simplifying the Testlease liability for Goodwill Impairment” (“ASU No. 2017-04”). To simplify the subsequent measurement of goodwill, ASU No. 2017-04 eliminates Step 2 from the goodwill impairment test. In computing the implied fair value of goodwill under Step 2, an entity had to perform procedures to determine the fair value at the impairment testing date of its assets and liabilities following the procedure that would be required in determining the fair value of assets acquired and liabilities assumed in a business combination. Instead, ASU No. 2017-04 requires an entity to perform its annual, or interim, goodwill impairment test by comparing the fair value of a reporting unit with its carrying amount. An entity should recognize an impairment charge for the amount by which the carrying amount exceeds the reporting unit’s fair value; however, the loss recognized should not exceed the total amount of goodwill allocated to that reporting unit. ASU No. 2017-04 also eliminates the requirements for any reporting unit with a zero or negative carrying amount to perform a qualitative assessment and, if it fails that qualitative test, to perform Step 2 of the goodwill impairment test. Therefore, the same impairment assessment applies to all reporting units. An entity is required to disclose the amount of goodwill allocated to each reporting unit with a zero or negative carrying amount of net assets. An entity still has the option to perform the qualitative assessment for a reporting unit to determine if the quantitative impairment test is necessary. ASU No. 2017-04most lease arrangements. The new standard is effective for fiscal years beginning after December 15, 2019.2018, with early adoption permitted, and must be adopted using the modified retrospective approach. The Company willintends to adopt the standard on the effective date of December 30, 2018. Interpretations are on-going and could have a material impact on the Company's implementation. Currently, the Company expects that the adoption of the ASU No. 2017-04 commencing in the first quarter of fiscal 2021. The Company does not believe this standard2016-02 (Topic 842) Leases will have a material impact on its financial statements orconsolidated balance sheet due to the related footnote disclosures.recognition of right-of-use assets and lease liabilities principally for certain leases currently accounted for as operating leases, and expects it to have a material impact on our results of operations.

 

Statement of Cash FlowsIn August 2016, the FASB issued ASU No. 2016-15, “Statement of Cash Flows (Topic 230): Classification of Certain Cash Receipts and Cash Payments (a consensus of the Emerging Issues Task Force)” (“ASU No. 2016-15”). ASU No. 2016-15 clarifies how certain cash receipts and payments should be presented in the statement of cash flows. ASU No. 2016-15 is effective for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2017. The Company will adopt ASU No. 2016-15 commencing inadopted the first quarternew standard effective July 1, 2018. The application of fiscal 2019. The Company does not believe this standard willdid not have a material impact on its financialthe Company’s unaudited condensed statements or the related footnote disclosures.of cash flows.

 

Note
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4. Patents, net

 

Patents, net consisted of the following (rounded to nearest thousand):

 

 

 

Useful life

 

 

March 31,

 

 

June 30,

 

 

 

(years)

 

 

2018

 

 

2017

 

 

 

 

 

 

 

 

 

 

 

Purchased Patent Rights – Brilacidin, and related compounds

 

14

 

 

$4,082,000

 

 

$4,082,000

 

Purchased Patent Rights – Anti-microbial – surfactants and related compounds

 

12

 

 

 

144,000

 

 

 

144,000

 

Patents – Kevetrin and related compounds

 

17

 

 

 

1,417,000

 

 

 

1,308,000

 

 

 

 

 

 

 

5,643,000

 

 

 

5,534,000

 

Less: Accumulated amortization for Brilacidin, Anti-microbial- surfactants and related compounds

 

 

 

 

 

(1,386,000)

 

 

(1,158,000)

Accumulated amortization for Patents –Kevetrin and related compounds

 

 

 

 

 

(225,000)

 

 

(164,000)

 

 

 

 

 

$4,032,000

 

 

$4,212,000

 

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Useful life

 

 

September 30,

2018

 

 

June 30,

2018

 

 

 

 

 

 

 

 

 

 

 

Purchased Patent Rights- Brilacidin, and related compounds

 

14

 

 

$4,082,000

 

 

$4,082,000

 

Purchased Patent Rights-Anti-microbial- surfactants and related compounds

 

12

 

 

 

144,000

 

 

 

144,000

 

Patents - Kevetrin and related compounds

 

17

 

 

 

1,238,000

 

 

 

1,219,000

 

 

 

 

 

 

 

5,464,000

 

 

 

5,445,000

 

Less: Accumulated amortization for Brilacidin, Anti-microbial- surfactants and related compounds

 

 

 

 

 

(1,538,000)

 

 

(1,462,000)

Accumulated amortization for Patents-Kevetrin and related compounds

 

 

 

 

 

(221,000)

 

 

(203,000)

Total

 

 

 

 

$3,705,000

 

 

$3,780,000

 

 

The patents are amortized on a straight-line basis over the useful lives of the assets, determined to be 12-17 years from the date of acquisition.

 

Amortization expense was approximately $96,000 and $95,000, for the three months ended March 31,September 30, 2018 and 2017 respectively and was approximately $289,000,$94,000 and $277,000 for the nine months ended March 31, 2018 and 2017,$96,000, respectively.

 

At March 31,September 30, 2018, the future amortization period for all patents was approximately 7.436.93 years to 16.75 years. Future estimated annual amortization expenses are approximately $96,000$282,000 for the year ending June 30, 2018, $383,0002019, $376,000 for each year from 20192020 to 2025, $374,000$367,000 for the year ending June 30, 2026, $371,000$364,000 for the year ending June 30, 2027, $134,000$127,000 for the year ending June 30, 2028, $80,000$73,000 for the years ending June 30, 2029 through the years ended 2031, $53,000 for the year ending June 30, 2032, $41,000$24,000 for the year ending June 30, 2033, $10,000$9,000 for the year ending June 30, 2034 and $2,000$3,000 for the year ending June 30, 2035.

 

Compounds with Activity Against Gram-Negative Bacteria and Fungi

As research at the Company is now focused on supporting its clinical trials, we have reduced costs associated with the licensing of intellectual property for gram-negative bacteria and anti-fungal compounds by returning our patent portfolio titled “Compounds and Methods for Treating Candidiasis and Aspergillus Infections” back to the university co-licensor. The Company at this time does not have any active gram-negative or anti-fungal programs and therefore has decided not to pay for the maintenance of these Patent Rights. The net book value of the impaired patent as of March 31, 2018 is not material.

Note 5. Accrued Expenses – Related Parties and Other

 

Accrued expenses consisted of the following (rounded to nearest thousand):

 

 

March 31,

 

June 30,

 

 

September 30,

2018

 

 

June 30,

2018

 

 

2018

 

 

2017

 

 

 

 

 

 

Accrued research and development consulting fees

 

$281,000

 

$673,000

 

 

$130,000

 

$208,000

 

Accrued rent (Note 8) – related parties

 

13,000

 

21,000

 

Accrued interest – (Note 9) related parties

 

 

12,000

 

 

 

17,000

 

Accrued rent (Note 8) - related parties

 

8,000

 

10,000

 

Accrued interest (Note 9) - related parties

 

 

36,000

 

 

 

48,000

 

 

 

 

 

 

Total

 

$306,000

 

 

$711,000

 

 

$174,000

 

 

$266,000

 

 

Note
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6. Accrued Salaries and Payroll Taxes - Related Parties andAnd Other

 

Accrued salaries and payroll taxes consisted of the following (rounded to nearest thousand):

 

 

March 31,

 

June 30,

 

 

September 30,

2018

 

 

June 30,

2018

 

 

2018

 

 

2017

 

 

 

 

 

 

Accrued salaries - related parties

 

$2,823,000

 

 

$2,823,000

 

 

$2,999,000

 

$2,823,000

 

Accrued payroll taxes - related parties

 

130,000

 

130,000

 

 

130,000

 

130,000

 

Accrued employee bonuses

 

-

 

86,000

 

 

114,000

 

214,000

 

Withholding tax - payroll

 

 

64,000

 

 

 

105,000

 

 

 

48,000

 

 

 

52,000

 

 

 

 

 

 

Total

 

$3,017,000

 

 

$3,144,000

 

 

$3,291,000

 

 

$3,219,000

 

 

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Note 7. Commitments and Contingencies

 

Lease Commitments

 

Operating Leases – Rental Property

 

The Company signed aOn September 30, 2018, the Company’s lease extension agreement with Cummings Properties which began on October 1, 2013.automatically renewed. The lease is for a term of five years ending on September 30, 2018,2023, and requires monthly payments of $18,000. Innovative Medical Research Inc., a company owned by Leo Ehrlich and Dr. Krishna Menon, officers of the Company, has co-signed the lease and subleases 200 square feet of space previously used by the Company and pays the Company $900 per month.approximately $19,000.

 

As of March 31,September 30, 2018, future minimum lease payments to Cummings Properties required under the non-cancelable operating lease are as follows (rounded to nearest thousand):

 

Year ending June 30,

 

 

 

 

 

 

2018

 

$54,000

 

2019

 

54,000

 

 

$228,000

 

Total minimum payments

 

$108,000

 

2020

 

228,000

 

2021

 

228,000

 

2022

 

228,000

 

2023

 

 

228,000

 

 

$1,140,000

 

 

Rent expense, net of lease income, under this operating lease agreement was approximately $53,000$52,000 and $52,000 for the three months ended March 31,September 30, 2018 and 2017, respectively and was approximately $157,000 and $153,000 for the nine months ended March 31, 2018 and 2017, respectively. Before September 2013, the Company paid rent to Kard Scientific for office space and details are shown at Note 8 - Related Party Transactions below.

Operating Leases - Equipment

We leased equipment under a non-cancelable operating lease that expired in April, 2018. As of March 31, 2018, there was no future minimum rental commitment for our operating lease for the next twelve months.

 

Contractual Commitments

 

The Company has total non-cancelable contractual minimum commitments of approximately $1.0$3 million to contract research organizations as of March 31,September 30, 2018. Expenses are recognized when services are performed by the contract research organizations.

 

Note
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8. Related Party Transactions

 

Office Lease

 

The Company charged Kard Scientific $1,800 for space for the two months of July and August, 2018. Dr. Menon, the Company’s principal shareholder, and former President of Research, and Director, also serves as the Chief Operating Officer and Director of Kard Scientific (“KARD”). On December 7, 2007,Scientific. Dr. Menon’s employment was terminated with the Company began renting office space from KARD, and sinceon September 18, 2018. Dr. Menon continues to serve on the Company’s Board of Directors. As of September 1, 2013, the Company2018, KARD no longer leases space from KARD. At March 31, 2018 and June 30, 2017, rent payable to KARD of approximately $13,000 and $21,000, respectively, were included in accrued expenses.

In September 2013, the Company signed a lease extension agreement with Cummings Properties for the company’s offices and laboratories at 100 Cummings Center, Suite 151-B Beverly, MA 01915. The lease is for a term of five years from October 1, 2013 to September 30, 2018 and requires monthly payments of approximately $18,000. The Company had taken over the space occupied by KARD. In addition, Innovative Medical Research Inc., (“Innovative Medical”) a company owned by Mr. Ehrlich and Dr. Menon, officers of the Company, has co-signed the lease and rents approximately 200 square feet of office space, the space previously used by the Company and pays the Company $900 per month, the same amount the Company previously paid KARD. Innovative Medical paid total rent of approximately $3,000 and $9,000 to the Company for both of the three months and nine months ended March 31, 2018 and 2017 and the rental payment was offset with the accrued rent owed to KARD.Company.

 

Clinical Studies

 

The Company previously engaged KARD to conduct specified pre-clinical studies. The Company did not have an exclusive arrangement with KARD. All work performed by KARD needed prior approval by the executive officers of the Company, and the Company retained all intellectual property resulting from the services by KARD. The Company now has its own research study capabilities and no longer uses KARD. At March 31,September 30, 2018 and June 30, 2017,2018, the accrued research and development expenses payable to KARD was approximately $1,486,000 and this amount was included in accounts payable.

 

Other related party transactions are disclosed in Note 9 below.

 

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Note 9. Convertible Note Payable - Related Party

 

During the year ended June 30, 2010, Mr. Ehrlich loaned the Company a total of approximately $973,000. A condition for this note was that the Ehrlich Promissory Note A and Ehrlich Promissory Note B be replaced with a new note, Ehrlich Promissory Note C. The Ehrlich Promissory Note C is an unsecured demand note that bears 9% simple interest per annum and is convertible into the Company’s Class A common stock at $0.50 per share. The note requires that the interest rate on the amounts due on Ehrlich Promissory Notes A and B be changed retroactively, beginning October 1, 2009, to 9%. On April 1, 2011, the Company amended the Ehrlich Promissory Note C and agreed to retroactively convert accrued interest of approximately $97,000 through December 31, 2010 into additional principal. During the year ended June 30, 2011, Mr. Ehrlich loaned the Company an additional (approximate)approximately $997,000 which brought the total balance of the demand note to approximately $2,002,000. During the year ended June 30, 2012, Mr. Ehrlich loaned the Company an additional $20,000 which brought the balance of this demand note to approximately $2,022,000.

 

On May 8, 2012, the Company did not have the ability to repay the Ehrlich Promissory Note C loan and agreed to change the interest rate on the outstanding balance of principal and interest of approximately $2,248,000, as of March 31, 2012, from 9% simple interest to 10% simple interest, and the Company issued 2,000,000 Equity Incentive Options exercisable at $0.51 per share equal to 110% of the closing bid price of $0.46 per share on May 7, 2012. Options are valid for ten (10) years from the date of issuance.

 

At March 31,As of September 30, 2018 and June 30, 2017,2018, approximately $12,000$36,000 and $17,000,$48,000, respectively, is the accrued interest payable on this note.

 

At March 31,As of September 30, 2018 and June 30, 2017,2018, principal balance of this demand note was approximately $2,022,000.

 

Note
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10. Equity Incentive Plans, Stock-Based Compensation, Exercise of Options and Warrants Outstanding

 

Current Equity Incentive PlanPlans

 

2016 Equity Incentive Plan

 

On June 30, 2016, the Board of Directors adopted the Company’s 2016 Equity Incentive Plan (the “2016 Plan”). The 2016 Plan became effective upon adoption by the Board of Directors on June 30, 2016.

 

Up to 20,000,000 shares of the Company’s Class A common stock may be issued under the 2016 Plan (subject to adjustment as described in the 2016 Plan); provided that (1) no Outside Director (as defined in the 2016 Plan) may be granted awards covering more than 250,000 shares of common stock in any year and (2) no participant shall be granted, during any one year period, options to purchase common stock and stock appreciation rights with respect to more than 4,000,000 shares of common stock in the aggregate or any other awards with respect to more than 2,500,000 shares of common stock in the aggregate. The 2016 Plan permits the grant of ISOs, non-qualified stock options, stock appreciation rights, restricted awards, performance share awards and performance compensation awards to employees, directors, and consultants of the Company and its affiliates.

 

In connection with adoption of the 2016 Plan, the Board of Directors also approved forms of Incentive Stock Option Agreement for Employees, Non-qualified Stock Option Agreement for Employees, Non-qualified Stock Option Agreement for Non-Employee Directors, Restricted Stock Award Agreement for Employees and Restricted Stock Award Agreement for Non-Employee Directors that will be utilized by the Company to grant options and restricted shares under the 2016 Plan.

 

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Stock Options Issued and Outstanding

 

The following table summarizes all stock option activity under the Company’s equity incentive plans:

 

 

 

Number of Options

 

 

Weighted Average Exercise Price

 

 

Weighted Average Remaining Contractual Life (Years)

 

 

Aggregate Intrinsic Value

 

Outstanding at June 30, 2017

 

 

40,655,245

 

 

$0.22

 

 

 

3.61

 

 

$31,662,730

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Granted

 

 

1,070,826

 

 

 

0.75

 

 

 

8.14

 

 

 

 

 

Forfeited/expired

 

 

(277,924)

 

 

2.44

 

 

 

 

 

 

 

 

 

Outstanding at March 31, 2018

 

 

41,448,147

 

 

 

0.22

 

 

 

3.01

 

 

$14,819,300

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Exercisable at March 31, 2018

 

 

40,452,299

 

 

 

0.21

 

 

 

2.87

 

 

$14,819,300

 

 

 

Number of
Options

 

 

Weighted

Average Exercise Price

 

 

Weighted Average Remaining Contractual Life

(Years)

 

 

Aggregate

Intrinsic Value

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Outstanding at June 30, 2018

 

 

41,643,571

 

 

 

0.22

 

 

 

2.76

 

 

$17,523,113

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Granted

 

 

795,826

 

 

 

0.40

 

 

 

10.0

 

 

 

 

 

Exercised

 

 

-

 

 

 

-

 

 

 

 

 

 

 

 

 

Forfeited/expired

 

 

(50,000)

 

 

2.49

 

 

 

 

 

 

 

 

 

Outstanding at September 30, 2018

 

 

42,389,397

 

 

 

0.22

 

 

 

2.65

 

 

$3,240,000

 

Exercisable at September 30, 2018

 

 

41,020,636

 

 

$0.21

 

 

 

2.43

 

 

$3,240,000

 

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The fair value of options granted for the ninethree months ended March 31,September 30, 2018 and 2017 was estimated on the date of grant using the Black Scholes model that uses assumptions noted in the following table.

 

 

Nine months ended

 

March 31,

 

Three months ended

September 30,

 

 

2018

 

2017

 

 

2018

 

 

2017

 

Expected term (in years)

 

5 - 10

 

3 - 10

 

 

10

 

10

 

Expected stock price volatility

 

52.80% to 106.01%

 

57.63% to 111.62%

 

 

104.11%

 

106.01%

Risk-free interest rate

 

2.15% to 2.56%

 

0.71% to 2.49%

 

 

2.86%

 

2.15%

Expected dividend yield

 

0

 

0

 

0

 

0

 

 

Stock-Based Compensation

 

The Company recognized approximately $265,000$229,000 and $336,000$369,000 of total stock-based compensation costs related to stock and stock optionsequity grant awards for the three months ended March 31,September 30, 2018 and 2017, respectively. The Company recognized approximately $1,665,000 and $1,026,000$229,000 of total stock-based compensation costs related to stock and stock options awards for the nine months ended March 31, 2018 and 2017, respectively.

The $1,665,000 of total stock-based compensation expense for the ninethree months ended March 31,September 30, 2018 included approximately $677,000$102,000 of stock options expense and $988,000$127,000 of restricted stock awards.

 

ForThe $369,000 of stock-based compensation expense for the ninethree months ended March 31,September 30, 2017 included approximately $141,000 of stock options expense and $228,000 of restricted stock awards. (see Note 11).

During the three months ended September 30, 2018

 

On FebruarySeptember 1, 2018, the Company agreed to issue options to purchase 75,000 shares of common stock to each of two consultants for specified services to be provided from February 1, 2018 to January 31, 2019 in accordance with agreements with the consultants. During the nine months ended March 31, 2018, the Company recorded approximately $8,000 of related stock-based compensation.

On February 10, 2017, the Company entered into verbal agreements with two consultants to issue options to purchase 50,000 shares of common stock and 75,000 shares of common stock, respectively, to the two consultants for services to be performed from February 13, 2017 to January 31, 2018 in accordance with their consulting agreements. The Company formally signed the agreements with the two consultants on March 13, 2018. During the nine months ended March 31, 2018, the Company recorded approximately $72,000 of related stock-based compensation.

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On September 1, 2017, the Company agreed to grantissued to Dr. Arthur Bertolino, the President and Chief Medical Officer of the Company, under the 2016 Plan (i)for his services rendered 1,066,667 shares of restricted stock and (ii) a ten-year option to purchase 617,839 shares of the Company’s Class A common stock, at an exercise price of $0.705 per share. Both shares and options shall vest upon the earliest to occur of the following: (1)vesting 50% upon the first anniversary of the effectivegrant date and the remaining 50% upon the second anniversary of the effective date; (2)grant date, with acceleration in certain circumstances as provided in the award agreement. The Company also issued 617,839 stock options to purchase shares of the Company’s common stock. These stock close above $3.00 per share (as may be adjusted for any stock splits or similar actions); (3) the commencement of trading of shares of the Company’s common stock on a national securities exchange; or (4) upon a change in control of the Company. The 1,066,667 shares wereoptions are valued at approximately $752,000$225,000, based on the closing bid price as quoted on the OTC on August 31, 2018 at $0.398 per share. These options were issued with an exercise price of $0.398 and vest 50% upon the 617,839 stock options valued at approximately $399,000. Both shares and options will be amortized over 2 years to September 1, 2019 unless the probabilityfirst anniversary of the other above vesting requirements occurring are met at an earlier date. At March 31, 2018,grant date and 50% upon the Company determined that it was not probable that these accelerated vesting provisions would occur earlier thansecond anniversary of the scheduled vesting date.grant date, with acceleration as defined in award agreement, with a ten year option term. These options have piggyback registration rights. During the three months and nine months ended March 31,September 30, 2018, the Company recorded approximately $144,000 and $336,000 of total stock-based compensation, respectively. The $144,000$26,000 of stock-based compensation expense for the three months ended March 31, 2018 includedthese equity grants, including approximately $50,000$9,000 of stock option expense and $94,000 of stock awards. The $336,000 of stock-based compensation expense$17,000 for the nine months ended March 31, 2018 included approximately $117,000 of stock option expense and $219,000 of stock awards.

 

On September 1, 2017,2018, the Company agreed to grantalso issued to Ms. Jane Harness, the Senior Vice President, Clinical Sciences and Portfolio Management of the Company, under the 2016 Plan (i) 58,394 shares of restricted stock and (ii) a ten-year option to purchase 172,987 shares of the Company’s Class A common stock, at an exercise price of $0.705 per share. Both shares and options shall vest upon the earliest to occur of the following: (1) one third33 1/3% vesting upon the first anniversary of the effectivegrant date, one third33 1/3% upon the second anniversary of the effectivegrant date and the remaining one third33 1/3% upon the third anniversary of the effective date; or (2) upon a changegrant date, with acceleration in control ofcertain circumstances as provided in the Company.award agreement. The 58,394 shares wereCompany also issued 172,987 options to purchase common stock. These stock options are valued at approximately $41,000 and$63,000, based on the 172,987 stock options valued at approximately $112,000. Both shares and options will be amortized over 3 years to September 1, 2020 unlessclosing bid price as quoted on the other vesting requirements are met sooner. During the three months and nine months ended MarchOTC on August 31, 2018 the Company recorded approximately $13,000 and $30,000 of total stock-based compensation, respectively. The $13,000 of stock-based compensation expense for the three months ended March 31, 2018 included approximately $9,000 of stock option expense and $4,000 of stock awards. The $30,000 of stock-based compensation expense for the nine months ended March 31, 2018 included approximately $22,000 of stock option expense and $8,000 of stock awards.

On September 1, 2017, the Company agreed to grant to Anne Ponugoti, under the 2016 Plan, ten-yearat $0.398 per share. These options to purchase 5,000 shares of the Company’s common stock atwere issued with an exercise price of $0.705 per share, which shall$0.398 and vest upon the earliest to occur of the following: (1) one third33 1/3% upon the first anniversary of the effectivegrant date, one-third33 1/3% upon the second anniversary of the effectivegrant date, and the remaining one-third33 1/3% upon the third anniversary of the effective date; or (2)grant date, with acceleration of vesting upon a change in control of the Company. The 5,000 stock options were valued at approximately $3,000 and will be amortized over 3 years to September 1, 2020 unless the other vesting requirements are met sooner.certain events. During the three months and nine months ended March 31,September 30, 2018, the Company recorded approximately $300 and $700 of stock option expense for this option grant.

On January 9, 2017, the Company and Ms. Ponugoti entered into an executive employment agreement as the Company’s Associate Director, Clinical Sciences, effective on February 1, 2017. Pursuant to the employment agreement, the Company issued 10,000 shares of restricted stock and options to purchase 30,000 shares of common stock under the 2016 Plan. During the three months and nine months ended March 31, 2018, the Company recorded approximately $3,000 and $9,000 of total stock-based compensation, respectively. The $3,000$2,000 of stock-based compensation expense for the three months ended March 31, 2018 includedthese equity grants, including approximately $2,000$1,000 of stock option expense and $1,000 offor the stock awards. The $10,000 of stock-based compensation expense for the nine months ended March 31, 2018 included approximately $7,000 of stock option expense and $3,000 of stock awards.

Purchase of Treasury Stock - cash paid to Federal and State Taxing Authorities arising from the withholding of common shares from officers’ vested restricted stock grant issuance and issuance of Treasury Stock and the reversal of outstanding stock subscription receivable

On September 1, 2017, 19,465 shares of the Company’s restricted stock vested to Ms. Harness according to Ms. Harness’s employment agreement. The total taxable compensation to Ms. Harness for the 19,465 vested shares was $14,000, which is priced at the closing stock price on September 1, 2017 at $0.705 a share.

The Company issued 12,409 common shares (net share issuance amount), which is approximately 64% of the total vested common share amount of 19,465 common shares due to be issued to Ms. Harness. The remaining 7,056 shares of common stock were withheld from Ms. Harness for the payment of payroll taxes to the Federal and State taxing authorities and these shares withheld are being reported by the Company as treasury stock, at cost, on the Company’s accompanying balance sheets.

On December 22, 2017, 533,334 shares of the Company’s restricted stock vested to Dr. Bertolino according to Dr. Bertolino’s employment agreement. The total taxable compensation to Dr. Bertolino for the 533,334 vested shares was $373,334, which is priced at the closing stock price on December 21, 2017 at $0.7 a share.

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The Company issued 295,286 common shares (net share issuance amount), which is approximately 55% of the total vested common share amount of 533,334 common shares due to be issued to Dr. Bertolino. The remaining 238,048 shares of common stock were withheld from Dr. Bertolino for the payment of payroll taxes to the Federal and State taxing authorities and these shares withheld are being reported by the Company as treasury stock, at cost, on the Company’s accompanying balance sheets.

In addition, the Company reversed an outstanding stock subscription receivable of $26,000 for 60,000 shares of common stock and recorded this amount as the cost of treasury stock.

On February 1, 2018, 3,333 shares of the Company’s restricted stock vested to Ms. Anne Ponugoti according to Ms. Ponugoti’s employment agreement. The total taxable compensation to Ms. Ponugoti for the 3,333 vested shares was $2,433, which is priced at the closing stock price on January 31, 2018 at $0.73 a share. The Company issued 2,645 common shares (net share issuance amount), which is approximately 79% of the total vested common share amount of 3,333 common shares due to be issued to Ms. Ponugoti. The remaining 688 shares of common stock were withheld from Ms. Ponugoti for the payment of payroll taxes to the Federal and State taxing authorities.

On February 5, 2018, the Board of Directors approved the retirement of 567,872 shares of its common stock in treasury, which shares are issued but are not outstanding. These shares included the 688 shares withheld from Ms. Ponugoti, as a result, all treasury shares of the Company were retired.

There were 0 shares and 262,080 shares of treasury stock outstanding at March 31, 2018 and June 30, 2017, respectively, purchased at a total cumulative cost of $0 and $220,000 at March 31, 2018 and June 30, 2017, respectively.

 

Restricted Stock Awards Outstanding

 

The following summarizes our restricted stock activity for our restricted stock issuances:

 

 

 

 

Weighted

 

 

 

 

Weighted

 

 

 

 

Average

 

 

 

 

Average

 

 

 

 

Grant

 

 

 

 

Grant

 

 

Number of

 

Date Fair

 

 

Number of

 

Date Fair

 

 

Shares

 

 

Value

 

 

Shares

 

 

Value

 

 

 

 

 

 

Total awards outstanding at June 30, 2017

 

601,728

 

$1.39

 

Total awards outstanding at June 30, 2018

 

1,208,157

 

$0.72

 

Total shares granted

 

1,125,061

 

0.71

 

 

1,130,061

 

$0.40

 

Total shares vested

 

(556,132)

 

1.40

 

 

(572,263)

 

$0.73

 

Total shares forfeited

 

 

 

 

 

 

 

 

 

 

-

 

 

$-

 

Total unvested shares outstanding at March 31, 2018

 

 

1,170,657

 

 

$0.73

 

Total unvested shares outstanding at September 30, 2018

 

 

1,765,955

 

 

$0.51

 

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Scheduled vesting for outstanding restricted stock awards at March 31,September 30, 2018 is as follows:

 

 

 

Year Ending June 30,

 

 

 

2018

 

 

2019

 

 

2020

 

 

2021

 

 

Total

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Scheduled vesting

 

 

0

 

 

 

575,596

 

 

 

575,597

 

 

 

19,464

 

 

 

1,170,657

 

 

 

Year Ending June 30,

 

 

 

2019

 

 

2020

 

 

2021

 

 

2022

 

 

Total

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Scheduled vesting

 

 

28,333

 

 

 

1,142,563

 

 

 

573,929

 

 

 

21,130

 

 

 

1,765,955

 

 

As of March 31,September 30, 2018, there was approximately $0.6$0.8 million of net unrecognized compensation cost related to unvested restricted stock-based compensation arrangements. This compensation is recognized on a straight-line basis resulting in approximately $0.4$0.6 million of compensation expected to be expensed over the next twelve months, and the total unrecognized stock-based compensation expense having a weighted average recognition period of 1.481.03 years.

Exercise of options

During the three months ended September 30, 2018 and 2017, there were no stock options exercised.

Stock Warrants Outstanding

During the three months ended September 30, 2018 and 2017, there were no warrants issued. On June 28, 2018, the Company issued warrants to purchase 8,000,000 shares of its common stock exercisable for 5 years at an exercise price of $0.38 per share. The warrants were recorded within stockholders’ deficiency. The fair value of the warrants issued on June 28, 2018 was estimated on the date of issuance using the Black Scholes Model that uses assumptions noted in the following table.

Expected term (in years)

3

Expected stock price volatility

82.36%

Risk-free interest rate

2.73%

Expected dividend yield

0

The following table summarizes the outstanding stock warrants: 

 

 

Warrants

 

 

Weighted Average Exercise Price

 

 

Weighted Average Remaining Contractual Life (Years)

 

 

Aggregate

Intrinsic Value

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Outstanding at June 30, 2018

 

 

8,000,000

 

 

$0.38

 

 

 

5.0

 

 

$-

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Extended

 

 

-

 

 

 

-

 

 

 

-

 

 

 

 

 

Granted

 

 

-

 

 

 

-

 

 

 

-

 

 

 

 

 

Exercised

 

 

-

 

 

 

-

 

 

 

-

 

 

 

 

 

Expired

 

 

-

 

 

 

-

 

 

 

-

 

 

 

 

 

Outstanding at September 30, 2018

 

8.000.000

 

 

$0.38

 

 

 

4.75

 

 

$-

 

 

 
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For the nine months ended March 31, 2017

Issuances of Common Stock and Stock Options – Pursuant to New Employment Agreements11. Equity Transactions

 

On June 27, 2016,28, 2018, we entered into a Securities Purchase Agreement with Aspire Capital Fund, LLC, pursuant to which the Company and Dr. Bertolino entered into an executive employment agreement as our President and Chief Medical Officer of the Company, effective on June 27, 2016 and the Companyhas agreed to grantsell up to Dr. Bertolino under the Company’s 2016 Equity Incentive Plan (i) 1,066,667 shares$7.0 million of restricted stock and (ii) a ten-year option to purchase 617,839 shares of the Company’s Class A common stock atto Aspire Capital, without an underwriter or placement agent.

Pursuant to the Securities Purchase Agreement, and in connection with Aspire Capital’s commitment to purchase additional securities from the Company, on June 28, 2018, the Company agreed to (i) sell to Aspire Capital 5,263,158 shares for a purchase price of $2.0 million and (ii) issue to Aspire Capital 2,736,842 shares of common stock and warrants to purchase 8,000,000 shares of common stock, with such warrants having an exercise price of $1.39 per share. Both shares and options shall vest upon the earliestequal to occur of the following: (1) 50% upon the first anniversary of the effective date, and the remaining 50% upon the second anniversary of the effective date (2) completion of both a Phase 2b psoriasis study and a Phase 2 oral mucositis study; (3) the Company’s common stock closes above $3.00$0.38 per share (as may be adjusted for any stock splits or similar actions); (4) the commencement of trading of the Company’s common stock on a national securities exchange (e.g. Nasdaq or the NYSE); or (5) upon a Change in Control of the Company (as defined in the employment agreement)(the “Commitment Fee”). The 1,066,667 shares were valued at approximately $1.5 million, which will be amortized over two years to June 27, 2018. The 617,839 stock options valued at approximately $800,000 and will be exercisable for 10 years at an exercise price of $1.39 per share. During the three months and nine months ended March 31, 2018, the Company recorded approximately $0 and $1,134,000 of total stock-based compensation, respectively. There was no stock-based compensation expenseSecurities Purchase Agreement provides for the three months ended March 31, 2018 for it was fully expensed. The $1,134,000sale of stock-based compensation expense for the nine months ended March 31, 2018 included approximately $396,000 of stock option expense and $738,000 of stock awards.

In December, 2017 and October, 2017, respectively, the Company was ableup to conclude both the Phase 2b psoriasis study and a Phase 2 oral mucositis study; therefore the remaining 50% of the shares and options vested to Dr. Bertolino, and all remaining shares and options granted on June 27, 2016 were fully amortized and expensed in December, 2017.

On July 18, 2016, the Company issued 7,500 stock options to purchase sharesan additional $5.0 million of the Company’s common stock to a consultant for services rendered, exercisable for 3 years at $1.38 per shareAspire Capital upon the achievement of common stock. certain milestones by September 30, 2018, which were not achieved by the Company. 

The valuetotal commitment fee of these 7,500 options$2.7 million was allocated to the $2 million offering first based on historical price discounts that Aspire Capital has received and the balance of the commitment fee was allocated to the $5 million of potential future milestone funding from Aspire Capital. The portion of the commitment fee allocated to the $2 million of initial proceeds was approximately $4,000. During$0.5 million and was effectively netted against the three months ended$2 million of initial proceeds, resulting in a discounted purchase price of $0.29 per share. The remaining $2.2 million of the commitment fee was allocated to the future milestone funding and was fully expensed under Other Expenses as of June, 30, 2018. As of September 30, 2016, the Company recorded approximately $4,000 of stock option expense for this option grant.

On September 1, 2016, the Company and Ms. Harness entered into an executive employment agreement as the Company’s VP, Clinical Sciences and Portfolio Management, effective on September 1, 2016. Commencing on September 1, 2016, the Company agreed to pay Ms. Harness an annual salary of $250,000. In addition, the Company agreed to grant to Ms. Harness, under the 2016 Plan (i) 58,394 shares of restricted stock, which shall vest upon the earliest to occur of the following: (1) one third upon the first anniversary of the effective date, one-third upon the second anniversary of the effective date, and the remaining one-third upon the third anniversary of the effective date; or (2) upon a Change in Control (as defined in the employment agreement) of the Company, and (ii) ten-year options to purchase 172,987 shares of the Company’s common stock were also granted at an exercise price of $1.37 per share, which shall vest upon the earliest to occur of the following: (1) one-third upon the first anniversary of the effective date, and the remaining balance vesting monthly in equal portions over the following 24 months; and (2) upon a Change in Control (as defined in the employment agreement) of the Company. The 58,394 shares were valued at approximately $80,000, which will be amortized over three years to September 1, 2019. The 172,987 stock options were valued at approximately $220,000 and will be exercisable for 10 years at an exercise price of $1.37 per share. They will be amortized over 3 years to September 1, 2019. During the three months and nine months ended March 31, 2018, the Company recorded approximately $25,000$5 million of milestone funding was not received and $75,000 of total stock-based compensation, respectively. The $25,000 of stock-based compensation expense for the three months ended March 31, 2018 included approximately $18,000 of stock option expense and $7,000 of stock awards. The $75,000 of stock-based compensation expense for the nine months ended March 31, 2018 included approximately $54,000 of stock option expense and $21,000 of stock awards.

Exercise of options

During the three months and nine months ended March 31, 2018 and 2017, there were no stock options exercised.

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Note 11. Equity Transactionsexpired.

 

$30 million Class A Common Stock Purchase Agreement with Aspire Capital

 

On September 6, 2017, the Company entered into a common stock purchase agreementthe Purchase Agreement with Aspire Capital, which replaced the prior 2015 $30 million Aspire Capital stock purchase agreement and provides that, upon the terms and subject to the conditions and limitations set forth therein, Aspire Capital is committed to purchase up to an aggregate of $30.0 million of the Company’s common stock over the 36-month term of the Stock Purchase Agreement. The Company issued 300,000 shares of its Class A common stock to Aspire Capital as a commitment fee. The commitment fee of approximately $215,000 is amortized pro-rata as the funding is received. The amortized amount of $41,000$55,000 was recorded to additional paid-in capital for the nine monthsyear ended March 31,June 30, 2018. The unamortized portion is carried on the balance sheet as deferred offering costs and was $173,000$159,000 at March 31,June 30, 2018 and September 30, 2018. The Company registered the sale of all shares that Aspire Capital will purchase under this common stock purchase agreement. To the extent Aspire Capital purchases shares under this Purchase Agreement and subsequently sells those shares purchased, the other holders of shares of our Class A common stock may experience dilution, which may be substantial. In addition, the sale of a substantial number of shares of our Class A common stock by Aspire Capital, or anticipation of such sales, could make it more difficult for us to sell equity or equity-related securities in the future at a time and price that we might otherwise wish to effect sales.

 

During the period from September 6, 2017 to March 31,September 30, 2018, the Company generated proceeds of approximately $5.7$7.7 million under the new 2017 agreement with Aspire Capital from the sale of approximately 8.79.5 million shares of its common stock. As of March 31,September 30, 2018, the available balance under the new equity line agreement was approximately $24.3$22.3 million. However, as of date of this report, the conditions for sales under the Purchase Agreement are not satisfied and no sales may occur thereunder. See Note 2, Going Concern and Liquidity.

 

On March 30, 2015, the Company entered into its prior common stock purchase agreement with Aspire Capital, which provided that, upon the terms and subject to the conditions and limitations set forth therein, Aspire Capital was committed to purchase up to an aggregate of $30.0 million of the Company’s common stock over the 36-month term of the Purchase Agreement.2015 purchase agreement. In consideration for entering into this stock purchase agreement, the Company issued to Aspire Capital 160,000 shares of its Class A common stock as a commitment fee. The commitment fee of approximately $499,000 was amortized as the funding was received. The unamortized portion of deferred offering costs from this stock purchase agreement of $227,000 was recorded to additional paid-in capital in September 2017, since the Company entered into a new $30 million common stock purchase agreement with Aspire Capital, to replace this prior $30 million 2015 Aspire Capital agreement, on September 6, 2017. During the period from July 1, 2017 to September 5, 2017, the Company generated proceeds of approximately $2.1 million under this 2015 agreement with Aspire Capital, from the sale of approximately 2.6 million shares of its common stock.

 

Note 12. Subsequent Events

Equity Transactions

From April 1, 2018 to May 9, 2018, the Company has generated additional proceeds of approximately $2.0 million under the Common Stock Purchase Agreement with Aspire Capital from the sale of approximately 8.0 million shares of its common stock.

 
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12. Subsequent Events

On October 5, 2018, the Company entered into a securities purchase agreement (the “Securities Purchase Agreement”) with one multi-family office for the sale of an aggregate of 2,000 shares of the Company’s newly-created Series B 5% convertible preferred stock (the “preferred stock”), for aggregate gross proceeds of approximately $2.0 million. An initial closing for the sale of 1,250 shares of preferred stock closed on October 9, 2018, and a subsequent closing for the sale of 750 shares of preferred stock closed on October 12, 2018. Under the Securities Purchase Agreement, the Company also issued to the investors warrants to purchase up to an additional 8,000 shares of preferred stock.

The rights and preferences of the preferred stock are set forth in a Certificate of Designation of Preferences, Rights and Limitations of Series B 5% Convertible Preferred Stock filed with the Nevada Secretary of State on October 5, 2018 (the “Certificate of Designation”). Each share of preferred stock has an initial stated value of $1,080 and may be converted at any time at the holder’s option into shares of the Company’s common stock at a conversion price equal of the lower of (i) $0.31625 per share and (ii) 85% of the lowest volume weighted average price of the Company’s common stock on a trading day during the ten trading days prior to and ending on, and including, the conversion date. The conversion price may be adjusted following certain triggering events and subsequent equity sales and is subject to appropriate adjustment in the event of stock splits, stock dividends, recapitalization or similar events affecting the Company’s common stock.

The holders of the preferred stock are limited in the amount of stated value of the preferred stock they can convert on any trading day. The conversion cap limits conversions by the holders to the greater of $75,000 and an amount equal to 30% of the aggregate dollar trading volume of the Company’s common stock for the five trading days immediately preceding, and including, the conversion date. However, the conversion cap will be increased if the trading volume in the first 30 minutes of any trading session exceeds certain trailing average daily volume amounts. In addition, the holders of the preferred stock may not convert shares of preferred stock if, after giving effect to the conversion, a holder together with its affiliates would beneficially own in excess of 9.99% of the outstanding shares of the Company’s common stock.

Following 30 days after the initial closing, the Company may elect to redeem the preferred stock for 120% of the aggregate stated value then outstanding, plus all accrued but unpaid dividends and all liquidated damages and other amounts due in respect of the preferred stock. The Company’s right to redeem the preferred stock is contingent upon it having complied with a number of conditions, including compliance with its obligations under the Certificate of Designation. Shares of preferred stock generally have no voting rights, except as required by law and except that the Company shall not take certain actions without the consent of the holders of the preferred stock.

Each share of preferred stock was sold together with three warrants: (i) a Series 1 warrant, which entitles the holder thereof to purchase 1.25 shares of preferred stock at $982.50 per share, or 2,500 shares of preferred stock in the aggregate for approximately $2.5 million in aggregate exercise price, for a period of up to nine months following issuance, (ii) a Series 2 warrant, which entitles the holder thereof to purchase 1.25 shares of preferred stock at $982.50 per share, or 2,500 shares of preferred stock in the aggregate for approximately $2.5 million in aggregate exercise price, for a period of up to 15 months following issuance, and (iii) a Series 3 warrant, which entitles the holder thereof to purchase 1.50 shares of preferred stock at $982.50 per share, or 3,000 shares of preferred stock in the aggregate for approximately $2.9 million in aggregate exercise price, for a period of up to 24 months following issuance.

Subject to the satisfaction of certain circumstances, the Company had the option to compel the holders to exercise up to $250,000 of the Series 1 warrants 30 days after the initial closing of the sale of the preferred stock. On November 2, 2018, the Company notified the holders of the warrants of the Company’s election to compel the exercise of $250,000 of warrants, which exercise is scheduled to occur on or about November 8, 2018. In addition, subject to the satisfaction of certain circumstances, the Company may call for cancellation any or all of the warrants following 90 days after their issuance, for a payment in cash equal to 8% of the aggregate exercise price of the warrants being called. The warrants subject to any such call notice will be cancelled 30 days following the Company’s payment of the call fee, provided that the warrant holders have not exercised the warrants prior to cancellation.

The Company intends to use the net proceeds from the offering for general corporate purposes, including research and development.

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ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

 

The following discussion and plan of operations should be read in conjunction with the condensed financial statements and the notes to those statements included in this Form 10-Q. This discussion includes forward-looking statements that involve risk and uncertainties. You should review our important note about forward-looking statements preceding the condensed financial statements in Item 1 of this Part I. As a result of many factors, such as those set forth under “Risk Factors” in this Form 10-Q and in our Annual Report on Form 10-K, actual results may differ materially from those anticipated in these forward-looking statements.

 

Management’s Plan of Operation

 

Overview

 

Innovation Pharmaceuticals Inc. is a clinical stage biopharmaceuticalpharmaceutical company developing innovative therapies for inflammatory diseases,with dermatology, oncology, dermatology,anti-inflammatory and anti-infectivesantibiotic applications. The Company owns the rights to numerous drug compounds, including Brilacidin, our lead drug in a new class of compounds called defensin-mimetics; Kevetrin (thioureidobutyronitrile), our lead anti-cancer compound; and Prurisol (KM-133), which is in development for psoriasis.psoriasis; and Kevetrin (thioureidobutyronitrile), our lead anti-cancer compound.

 

Effective JuneRecent Developments

Preferred Stock Offering. On October 5, 2017,2018, the Company changedentered into a securities purchase agreement with one multi-family office resulting in aggregate gross proceeds of approximately $2.0 million. These funds, and any other additional funds that might be received per the agreement (up to an additional approximately $7.7 million), will be used to advance business development and clinical pipeline objectives. See “Liquidity and Capital Resources” below for additional information.

Lease Extension. In September 2013, the Company signed a five-year lease agreement with Cummings Properties for the Company’s offices and laboratories at 100 Cummings Center, Suite 151-B Beverly, MA 01915. The lease included an automatic renewal provision for a term of five years from September 30, 2018 to September 30, 2023, and requires monthly payments of approximately $19,000. The total square footage of the space is substantially more than what is currently needed for our operations; the majority of the space is a laboratory. The Company believes, however, that if we are successful with advancing our Brilacidin Oral Mucositis and/or Prurisol Psoriasis programs into confirmatory studies, we will need all, or most of, the space as we could save substantial monies by doing in house functions that would otherwise be outsourced to contract research organizations. In the interim, we are planning to sublet laboratory space as we are now focused on conducting clinical studies.

On October 23, 2018 the Company was notified that the U.S. Food and Drug Administration (FDA) granted an End-of-Phase 2 (EoP2) meeting scheduled for later this quarter for Brilacidin OM program. The EoP2 meeting will help the Company align with the FDA on clinical trial design and other program requirements, the goal of which is to minimize unnecessary expenditures and speed the drug development process.

Business Development and Licensing

The Company is actively engaged in business development and licensing initiatives with multiple specialty and global pharmaceutical companies across its nameentire pipeline of drugs. From time to time, the Company may be party to various indications of interest and term sheets and participate in preliminary discussions and negotiations regarding potential licensing or partnership arrangements. It remains the Company’s primary objective to complete licensing deals, territorial and/or global, to provide access to non-dilutive capital to advance clinical assets forward in the most expeditious and cost-effective manner. The Company can make no assurance that partnerships will occur, but is committed toward executing on these potential alliance and partnership opportunities.

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Clinical Development Programs

Compound

Target/Indication

Clinical Status

Brilacidin

Oral Mucositis

Phase 2 Study (completed)

Inflammatory Bowel Disease

Phase 2 Proof of Concept Study (completed)

ABSSSI (Acute Bacterial Skin and Skin Structure Infection)

Phase 2 (completed)

Prurisol

Psoriasis

Phase 2b (completed)

Kevetrin

Ovarian Cancer

Phase 2 Study (completed)

We have no product sales to date and we will not receive any product revenue until we receive approval from Cellceutix Corporationthe FDA or equivalent foreign regulatory agencies to Innovation Pharmaceuticals Inc.begin marketing a pharmaceutical product. Developing pharmaceutical products, however, is a lengthy and very expensive process. Assuming we do not encounter any unforeseen safety or efficacy issues during the course of developing our product candidates, we do not expect to complete the development of a product candidate for several years, if ever.

 

The Company devotes most of its efforts and resources on business developmentits compounds which have reached clinical trials: Brilacidin oral rinse for the prevention of severe Oral Mucositis in Head and Neck Cancer patients receiving chemoradiation, Brilacidin for the clinical trialstreatment of its compounds.

Business Development Activities

The Company is engaged in discussionsAcute Bacterial Skin and negotiations regardingSkin Structure Infections (ABSSSI), and Brilacidin for Inflammatory Bowel Diseases; Prurisol for the out-licensingtreatment of its mid-stage, first-in-class clinical assets to global and/or specialty pharmaceutical companies who have expressed an interest in one or more assets in our pipeline. Successfully securing partnerships would affordPsoriasis; and Kevetrin for the Company access to immediate and potentially recurring sourcestreatment of non-dilutive capital, including upfront fees, milestone-based payments and tiered royalties.

Recently, we released results from our completed Phase 2 Brilacidin study on Oral Mucositis. The results have attracted inquiries, additional confidential disclosure agreements, and discussions with pharmaceutical companies.

Clinical Development Programs

cancer. We anticipate using our expertise to manage and perform what we believe are the most critical aspects of the product development process which include: (i) design and oversight of clinical trials; (ii) development and execution of strategies for the protection and maintenance of intellectual property rights; and (iii) interactions with regulatory authorities domestically and internationally. We expect to concentrate on product development and engage in a limited way in product discovery, avoiding the significant investment of time and financial resources that is generally required for a promising compound to be identified and brought into clinical trials.

 

Set forth below is an overview our research and development efforts on Brilacidin, Prurisol, and Kevetrin during fiscal 2019 and through the date of this Quarterly Report on Form 10-Q:

Brilacidin

Topical Brilacidin Clinical Studies (trials)

Compound

·Two trials of topical Brilacidin have been completed: a double-blind Phase 2 clinical trial of Brilacidin-OM for the treatment of Oral Mucositis (OM); and the other an open-label Phase 2 Proof-of-Concept (P-o-C) trial of Brilacidin for the treatment of Ulcerative Proctitis/Proctosigmoiditis (UP/UPS), two types of Inflammatory Bowel Diseases (IBD).

 

Target/Indication

·Oral Mucositis (OM) study In this randomized, double-blind Phase 2 study of Brilacidin for the prevention and control of OM in patients receiving chemoradiation for treatment of head and neck cancer, analysis of patients who received at least 55 Gy cumulative units of radiation showed that Brilacidin markedly reduced the rate of severe OM (WHO Grade ≥ 3), delayed onset of severe OM and decreased duration of severe OM. The Company made available, in a blog published on its website, a comparative data table (based on public information) showing Brilacidin compares favorably to other compounds in development for preventing and treating severe OM.

 

Clinical Status

Brilacidin

·

Oral Mucositis

IBD/UP/UPS study — This Phase 2 (Completed; Fast Track Designation)

2a trial comprises three sequential cohorts, with progressive dose escalation by cohort—cohort A (6 patients) - 50 mg, cohort B (6 patients) - 100 mg, and cohort C (5 patients) - 200 mg, respectively. Treatment with Brilacidin by daily enema administration was performed for 42 days. The primary efficacy endpoint of clinical remission (accounting for stool frequency, rectal bleeding and endoscopy findings subscores) was met by the majority of patients across the cohorts. Brilacidin was generally well-tolerated. Patient quality of life (as assessed by the short inflammatory bowel disease questionnaire, or SIBDQ) showed notable improvements. Limited systemic exposure to Brilacidin was demonstrated as measured by plasma Brilacidin concentrations.

Inflammatory Bowel Disease

Phase 2 (Completed; Proof of Concept Study)

*ABSSSI

Phase 2b (Completed; **QIDP; Fast Track Designation)

Kevetrin

Ovarian Cancer

Phase 2 (Completed; Orphan Drug Designation)

Prurisol

Psoriasis

Phase 2b (Completed)

________________

*ABSSSI- Acute Bacterial Skin

In order to obtain maximum value of the Brilacidin-IBD asset, based on feedback from some of the world’s leading pharmaceutical companies in this therapeutic area, we plan to develop this asset as an oral dose (pill or tablet), complete a microbiome study in healthy volunteers, and Skin Structure Infection **Qualified Infectious Disease Productperform a placebo-controlled study.

 

 
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Recent Developments

In early 2018, the Company approved steps to focus its efforts on clinical trials for its lead drug candidates. The Company’s office and laboratory needs have shifted from compound discovery to clinical development programs. The Company is now in the process of searching sites for its future headquarters.

The Company’s common stock traded under the stock symbol “CTIX” on the OTCQB until the market close of June 8, 2017. As of June 9, 2017, trading on the OTCQB began under the new Innovation Pharmaceuticals name and ticker symbol “IPIX”.

We are a clinical stage company. We have no product sales to date and we will not receive any product revenue until we receive approval from the FDA or equivalent foreign regulatory agencies to begin marketing a pharmaceutical product. Developing pharmaceutical products, however, is a lengthy and very expensive process. Assuming we do not encounter any unforeseen safety or efficacy issues during the course of developing our product candidates, we do not expect to complete the development of a product candidate for several years, if ever.

Set forth below is an overview of our research and development efforts on Brilacidin, Kevetrin, and Prurisol during fiscal 2018 and through the date of this Quarterly Report on Form 10-Q. We have entered into multiple non-disclosure agreements with large and mid-sized pharmaceutical companies that enable us to continue ongoing discussions regarding potential partnering should the below trial results support such a relationship.

Brilacidin

This lead drug candidate is in a new immunomodulatory class with anti-inflammatory and antibiotic properties called defensin-mimetics. Modeled after Host Defense Proteins (HDPs), the “front-line” of defense in the immune system, it is a small, non-peptidic, synthetic molecule that kills pathogens swiftly and thoroughly. Just as importantly, Brilacidin also functions in a robust immunomodulatory capacity, lessening inflammation and promoting healing.

Topical Brilacidin Clinical Studies (Trials)

In October 2017, the Company completed, a double-blind Phase 2 clinical trial of Brilacidin-OM for the treatment of oral mucositis (OM). In July 2017, the Company completed an open-label Phase 2 Proof-of-Concept (PoC) trial for the treatment of ulcerative proctitis /proctosigmoiditis (UP/UPS), two types of Inflammatory Bowel Diseases (IBD).

Oral Mucositis (OM): This completed study was a randomized, double-blind, placebo-controlled, Phase 2 clinical trial of Brilacidin for the prevention and control of Oral Mucositis (OM) in patients receiving chemoradiation for treatment of Head and Neck Cancer. Analysis of patients who received at least 55 Gy cumulative units of radiation showed the use of Brilacidin-OM met its primary endpoint with a clearly reduced incidence of severe OM (SOM) (WHO Grade ≥ 3) compared to placebo. Brilacidin oral rinse also appeared to be safe and well-tolerated.

Overall results were:

·Reduced Incidence of severe OM (Primary Endpoint)

oBrilacidin 42.9%, Placebo 60.0% [Modified Intent to Treat (mITT) Population]

oBrilacidin 36.8%, Placebo 60.0% [Per Protocol (PP) Population]

·Delayed Onset of severe OM

oFor those patients in the Brilacidin group who did experience severe OM, onset occurred generally later during radiation therapy. The clear separation between placebo and Brilacidin, as to time of onset of severe OM, can be seen in Kaplan-Meier curves.

·Reduced Duration of severe OM

oMedian durations for Brilacidin in both the mITT and PP populations for ‘initial instance’ and overall calculations were 0.0 days, indicating that more than half of all patients on active treatment did not experience severe OM. Overall median durations for placebo were 3.0 days and 5.5 days for the mITT and PP populations, respectively.

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Relative risk reduction in severe Oral Mucositis (WHO Grade ≥ 3) in the Brilacidin-OM treatment group from that seen in the control group ([incidence control- incidence active]/incidence control) was: 28.5% (mITT population) and 38.7% (PP population).

Brilacidin appeared to be more effective with a cisplatin chemotherapy regimen administered approximately every 21 days vs. weekly administration. Brilacidin reduced the incidence of severe OM (WHO Grade ≥3) in the subgroup of patients receiving cisplatin administered as a high-dose regimen (80-100 mg/m2) approximately every 21 days compared to placebo. For the mITT population, the incidence of severe OM in the placebo subgroup was 71.4%, whereas the incidence for the Brilacidin subgroup was reduced to 25.0% (p=0.048). For the PP population, the incidence of severe OM in the placebo subgroup was 72.7%, whereas the incidence for the Brilacidin subgroup was reduced to 14.3% (p=0.025). In addition, time to onset of severe OM was delayed with Brilacidin treatment compared to placebo, even more markedly in the 21-day cisplatin regimen subset.

The relative risk reduction in the incidence of severe OM, Brilacidin compared to placebo, for the approximately every 21 days cisplatin regimen subset is 65.0% (mITT population) and 80.3% (PP population).

The Company believes that Brilacidin-OM, with its granted Fast Track FDA designation, occupies a lead position among OM drug candidates currently advancing in competitive clinical pipelines.

Ulcerative proctitis /proctosigmoiditis (UP/UPS): The completed Phase 2a trial comprised of three sequential cohorts, with progressive dose escalation by cohort—Cohort A (6 patients) -50 mg, Cohort B (6 patients) - 100 mg, and Cohort C (5 patients) - 200 mg, respectively. Treatment with Brilacidin by daily enema administration was performed for 42 days. The Primary Efficacy Endpoint of Clinical Remission (accounting for Stool Frequency, Rectal Bleeding and Endoscopy Findings subscores) was met by the majority of patients across the cohorts. Brilacidin was generally well-tolerated. Patient Quality of Life (as assessed by the Short Inflammatory Bowel Disease Questionnaire or “SIBDQ”) showed notable improvements. Limited systemic exposure to Brilacidin was demonstrated as measured by plasma Brilacidin concentrations.

From these results, we see significant opportunities in more broadly treating Inflammatory Bowel Disease (IBD) with Brilacidin. Our development programs depending on available financial resources include new formulations (oral and foam type) with potential associated toxicology studies and clinical studies to be defined.

  

ABSSSI

 

In February 2016, the Company submitted a Special Protocol Assessment (SPA) request, along with a final protocol, to the FDA, for a Phase 3 clinical trial of Brilacidin for the treatment of Acute Bacterial Skin and Skin Structure Infection (ABSSSI) caused by Gram-positivegram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). We received from the FDA comments and considerations from the FDA for incorporation into our study design. Management has decided to delay its response to FDA due to the low price per share of our common stock and the approximateapproximately $30 million costs required for this study, the financing of which would likely result in significant dilution to our shareholders. Our strategy, for now, is to achieve success with other trials and attract partnering opportunities withthat may provide significant down-paymentsupfront payments and milestone payments, which can then be used to fund these trials.the ABSSSI program. Although we recognize significant generic competition for treating ABSSSI, we see ABSSSI as the appropriate gateway indication in infectious diseases, enabling potential further studies of Brilacidin’s use for implant coating and biofilm infections.

 

Our expendituresAs stated above, we see significant opportunities in treating IBD with Brilacidin. These data suggest that other inflammatory conditions including various dermatology disorders and conditions may, likewise, be treated locally and efficaciously with Brilacidin.

Expenditures on Brilacidin were approximately $1.5$0.4 million and $1.3$0.6 million during the nine monthsquarter ended March 31,September 30, 2018 and 2017, respectively.

 

KevetrinPrurisol

Kevetrin, our lead anti-cancer compound, is a small molecule compound that modulates p53, a protein involved in controlling cell mutations. In the majority of all cancers, regardless of origin, the p53 pathway is mutated, compromising its anti-tumor functions. In particular, most epithelial ovarian cancer patients have high-grade serous cancer, characterized by near universal p53 gene abnormalities. Pre-clinical research has demonstrated Kevetrin’s unique mechanism of action to induce apoptosis, slow tumor progression and reduce tumor volume in many types of cancers, including lung, breast, colon, prostate, squamous cell carcinoma and a leukemia tumor model. The FDA has awarded Orphan Drug designations for Kevetrin for ovarian cancer, retinoblastoma and pancreatic cancer as well as Rare Pediatric Disease designation for Retinoblastoma.

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The main objectiveCompany has completed a randomized, double-blind, parallel-group, placebo-controlled Phase 2b trial of Prurisol for approximately 189 subjects with moderate to severe plaque psoriasis. The treatment group arms are Prurisol 300mg, Placebo, Prurisol 400mg (Ratio 3:3:1) with a treatment duration of 12 weeks. We currently await statistical analysis of the Company’sresults pending payment by the Company of amounts due to the research organization resulting in part from cost overruns. A partial payment was made recently after the Company secured additional financing, with additional payments planned. Further clinical development of the Prurisol program will be determined once full study data are unblinded and available for analysis.

Expenditures on Prurisol were approximately $0.1 million and $1.8 million during the quarter ended September 30, 2018 and 2017, respectively. We expect expenditures on Prurisol to continue in future reporting periods, as we complete analysis of the study. We have entered into multiple non-disclosure agreements with pharmaceutical companies that enable us to continue ongoing discussions regarding potential partnering should the trial results support such a relationship.

Kevetrin

The company has completed a Phase 2a trial of Kevetrin in treating late-stage ovarian cancer was to confirmOvarian Cancer. The main objective of the trial focused on confirming the modulation by Kevetrin of p53 pathways in tumors, as well as monitoring the response of tumors to the treatment. This goalThe study was met with positive data from the first patients treated, showing direct evidencesuccessful in demonstrating modulation of molecular pathways modulationp53 directly in tumors. Modulationovarian cancer tumor tissue in patients. We are currently focused on development of the p53 protein was observed in response to administrationan oral formulation of Kevetrin; pathways analyses also pointed to concomitant cell cycle modulation at the level of gene expression. The Company believes that further pathways details and clinical tumor responses would best be explored with more frequent and potentially higher systemic drug exposure.Kevetrin for treating cancer. Pharmacokinetic data collected on Kevetrin during the initial Phase 1 clinical trial demonstrates that the compound has a short half-life of approximately two hours. Kevetrin’s short half-life makes it a compelling candidate for an oral drug delivery treatment for the main purpose of allowing simple daily, or multiple-times daily, administrations within or outside the hospital setting. Compared to injectable or intravenous treatments, oral therapy is the preferred drug delivery method of patients. Preliminary laboratory studies are encouraging and support the potential of developing an oral formulation, but there are no assurances made or implied that the Company will be successful in completing development of an oral formulation. The Company has completedToxicology studies for the oral formulation of Kevetrin are approximately half the Toxicology studies to support progression to oral dosing in humans, butcompleted, with the remainder of this work is on hold untilnow prioritized given the Company secureshas secured additional financial resources. Next steps in the development of Kevetrin include: completing toxicology work for an oral formulation; developing the oral formulation (pill or tablet); requesting an FDA meeting to discuss trial results to date and the design of future trials; and performing a dosing safety study in healthy volunteers once the oral formulation has been developed. Once completed, these steps would likely lead directly to Phase 2 testing of oral Kevetrin in both solid tumors and leukemias, with ovarian cancer likely continuing to be the lead indication.

 

Our expendituresExpenditures on Kevetrin were approximately $0.3$0.1 million and $0.7$0.1 million during the nine monthsquarter ended March 31,September 30, 2018 and 2017, respectively.

 

Prurisol
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Prurisol, our lead anti-psoriasis drug candidate, is a small molecule compound acting on the principles of immune modulation and PRINS (Psoriasis susceptibility-related RNA Gene Induced by Stress) reduction that has been found to be effective against psoriasis in animal models, both in induced psoriasis as well as a xenograft model with human psoriatic tissue.

The Company recently completed a randomized, double-blind, parallel-group, placebo-controlled Phase 2b trial of Prurisol for patients with moderate to severe plaque psoriasis. The treatment group arms are Prurisol 300mg, Placebo, Prurisol 400mg (Ratio 3:3:1) with a treatment duration of twelve weeks.Going Concern

 

We are currently awaiting data fromhave identified conditions and events that raise substantial doubt about our ability to continue as a going concern. At September 30, 2018, the trial. Our expenditures on Prurisol were approximately $3.8Company’s cash amounted to $0.3 million and $2.7current liabilities amounted to $8.3 million, during the nine months ended March 31, 2018 and 2017, respectively.

Future expenditures on Prurisol will be determined by the trial results, when available.

Compoundsof which $6.7 million were payables to related parties with Activity Against Gram-Negative Bacteria and Fungi

As research at theno immediate payment terms. The Company is now focused on supporting its clinical trials, we have reduced costs associated with the licensing of intellectual property for gram-negative bacteria and anti-fungal compounds by returning our  patent portfolio titled “Compounds and Methods for Treating Candidiasis and Aspergillus Infections” back to the university co-licensor. The Company at this timea development stage pharmaceutical company that has no sales as it does not have any active gram-negative  or anti-fungal programsproducts in the market and thereforewill continue to not have any revenues until it begins to market its products after it has decided notobtained the necessary FDA approval. As a result, the Company expects to paycontinue to incur losses over the next 12 months from the date of this filing. Accordingly, the Company’s planned operations, including total budgeted expenditures of approximately $14 million for the maintenancenext twelve months, raise doubt about its ability to continue as a going concern. If we are not able to continue as a going concern, it is likely that holders of these Patent Rights.our common stock will lose all of their investment. Our condensed financial statements do not include any adjustments that might result from the outcome of this uncertainty.

To continue as a going concern, we must secure additional funding to support our current operating plan. The net book value ofCompany expects to seek to obtain additional funding through business development activities (i.e. licensing and partnerships) and future equity issuances. There can be no assurance as to the impaired patent as of March 31, 2018 is not material.availability or terms upon which such financing and capital might be available.

 

Critical Accounting Policies and Estimates

 

Management’s discussion and analysis of financial condition and results of operations are based upon our accompanying condensed financial statements, which have been prepared in conformity with U.S. GAAP, and which requires us to make estimates and assumptions that affect the reported amounts of assets, liabilities, revenue and expenses, and related disclosure of contingent assets and liabilities. We base our estimates on historical experience and on various other assumptions that we believe are reasonable under the circumstances. These estimates are the basis for our judgments about the carrying values of assets and liabilities, which in turn may impact our reported revenue and expenses. Our actual results could differ significantly from these estimates under different assumptions or conditions.

 

Please see Note 3 of the condensed financial statements included in Part I, Item 1 of this Quarterly Report on Form 10-Q for the summary of significant accounting policies. In addition, please see Part II, Item 7, “Critical Accounting Policies and Estimates” in our Annual Report on Form 10-K for the year ended June 30, 2017.2018. There have been no material changes to our critical accounting policies and estimates since our Annual Report on Form 10-K for the year ended June 30, 2017.2018.

 

Recently Issued Accounting Pronouncements

 

Please see Note 3 to the Financial Statements,condensed financial statements, Significant Accounting Policies and Recent Accounting Pronouncements, in the accompanying notes to Financial Statements for a discussion of recent accounting pronouncements and their effect, if any, on our condensed financial statements.

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Results of Operations

 

We expect to incur losses from operations for the next few years. We expect to incur increasing research and development expenses, including expenses related to additional clinical trials for our proprietary programs. We expect that our general and administrative expenses will also increase in the future as we expand our business development, by adding employees, consultants, additional infrastructure and incurring other additional costs. Based upon our expected rate of expenditures over the next twelve months and beyond, we will need additional working capital to meet our anticipated clinical trial obligations and other working capital requirements.

 

For the three months ended March 31, 2018 and 2017

Revenue

 

We generated no revenue and incurred operating expenses of approximately $2.4$2.0 million and $3.9$4.5 million for the three months ended March 31,September 30, 2018 and 2017, respectively.

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Research and Development Expenses for Proprietary Programs

 

Below is a summary of our research and development expenses for our proprietary programs by categories of costs for the three months ended March 31,September 30, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

For the three months ended

 

Change

 

 

For the three months ended

 

Change

 

 

March 31

 

2018 vs. 2017

 

 

September 30,

 

2019 vs. 2018

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Clinical studies and development research

 

$1,040,000

 

$2,119,000

 

(1,079,000)

 

-51

%

 

$617,000

 

$2,783,000

 

(2,166,000)

 

(78)%

Officers’ payroll and payroll tax expenses related to R&D Department

 

174,000

 

232,000

 

(58,000)

 

-25

%

 

233,000

 

218,000

 

15,000

 

7%

Employees payroll and payroll tax expenses related to R&D Department

 

192,000

 

392,000

 

(200,000)

 

-51

 

184,000

 

330,000

 

(146,000)

 

(44)%

Stock-based compensation - officers

 

144,000

 

283,000

 

(139,000)

 

-49

 

172,000

 

337,000

 

(165,000)

 

(49)%

Stock-based compensation - employees

 

41,000

 

48,000

 

(7,000)

 

-15

%

 

44,000

 

32,000

 

12,000

 

38%

Stock-based compensation - consultants

 

80,000

 

5,000

 

75,000

 

1,500%

 

13,000

 

-

 

13,000

 

-

Depreciation and amortization expenses

 

 

105,000

 

 

 

103,000

 

 

 

2,000

 

 

 

2%

 

 

94,000

 

 

 

105,000

 

 

 

(11,000)

 

 

(10)%

Total

 

$1,776,000

 

 

$3,182,000

 

 

 

(1,406,000)

 

 

-44

 

$1,357,000

 

 

$3,805,000

 

 

 

(2,448,000)

 

 

(64)%

 

Research and development expenses for proprietary programs decreased during the three months ended March 31,September 30, 2018 primarily due to lowerless spending on our Brilacidin program and Prurisol program.

Officers’ payroll decreased due to the reduction in salary of one officer, which became effective on January 16, 2018.programs. Clinical studies and development expenses may decrease in future reporting periods depending on the Company’s current and future financial liquidity.

 

Officers’ payroll increased due to the increase in accrued bonus, offset by a 50% reduction in salary of Dr. Krishna Menon, the Company’s President of Research. In addition, Dr. Menon’s employment with the Company was terminated on September 18, 2018. Dr. Menon continues to serve on the Company’s Board of Directors.

Employees payroll and payroll tax expenses decreased during the three months ended March 31,September 30, 2018 related to fewer employees engaged in preclinical development in September,after December 31, 2017, which led to the decrease in employees’ payroll during the quarter ended March 31,September 30, 2018.

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Stock- based compensation - officers decreased during the three months ended March 31,September 30, 2018 primarily related to the decrease in the valuation of the annual stock-based compensation given to our new President and Chief Medical Officer on September 1, 2017 andan officer due to the vesting milestones fordecrease in the stocks and options granted to our President and Chief Medical Officer on June 27, 2016 became fully vested and expensed for the completed clinical trials in December, 2017.Company’s stock price.

 

Stock-based compensation- employee decreasedincreased during the three months ended March 31,September 30, 2018 due to the decreaseincrease vesting in the number of stock awards granted to employees during the quarter ended March 31,September 30, 2018 compared with the same period in 2017.

 

Stock-based compensation- consultant increased during the three months ended March 31,September 30, 2018 due to more stock awards were granted to consultants during the quarter ended March 31,September 30, 2018.

 

Our research and development expenses include costs related to preclinical and clinical trials, outsourced services and consulting, officers’ payroll and related payroll tax expenses, other wages and related payroll tax expenses, stock-based compensation, depreciation and amortization expenses. We manage our proprietary programs based on scientific data and achievement of research plan goals. Our scientists record their time to specific projects when possible; however, many activities occurring simultaneously benefit multiple projects and cannot be readily attributed to a specific project. Accordingly, the accurate assignment of time and costs to a specific project is difficult and may not give a true indication of the actual costs of a particular project. As a result, we do not report costs on an individual program basis.

 

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General and Administrative Expenses

 

General and administrative expenses consist mainly of compensation and associated fringe benefits not included in cost of research and development expenses for proprietary programs and include other management, business development, accounting, information technology and administration costs, including patent filing and prosecution, recruiting, consulting and professional services, travel and meals, facilities, depreciation and other office expenses.

 

Below is a summary of our general and administrative expenses for the three months ended March 31,September 30, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

For the three months ended

 

Change

 

 

For the three months ended

 

Change

 

 

March 31

 

2018 vs. 2017

 

 

September 30,

 

2019 vs. 2018

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Insurance and health expense

 

$112,000

 

$127,000

 

(15,000)

 

-12

%

 

$131,000

 

$127,000

 

4,000

 

3%

Rent and utility expense

 

64,000

 

70,000

 

(6,000)

 

-9

%

 

61,000

 

62,000

 

(1,000)

 

(2)%

Other G&A

 

 

119,000

 

 

 

134,000

 

 

 

(15,000)

 

 

-11

%

 

 

68,000

 

 

 

108,000

 

 

 

(40,000)

 

 

(37)%

Total

 

$295,000

 

 

$331,000

 

 

 

(36,000)

 

 

-11

%

 

$260,000

 

 

$297,000

 

 

 

(37,000)

 

 

(12)%

 

General and administrative expenses decreased during the three months ended March 31,September 30, 2018 primarily related to decreases in promotion, advertising and office expenses.

 

Officers’ Payroll and Payroll Tax Expenses

 

Below is a summary of our Officers’ payroll and payroll tax expenses for the three months ended March 31,September 30, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

 

Three months ended

 

 

Change

 

 

 

March 31

 

 

2018 vs. 2017

 

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Officers’ payroll and payroll tax expenses

 

$132,000

 

 

$138,000

 

 

 

(6,000)

 

 

-4

%

 

 

Three months ended

 

 

Change

 

 

 

September 30,

 

 

2019 vs. 2018

 

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Officers’ payroll and payroll tax expenses

 

$123,000

 

 

$130,000

 

 

 

(7,000)

 

 

(5)%

 

Officers’ payroll and payroll tax expenses for the Company was decreased during the three months ended March 31,September 30, 2018 and 2017. The officers’ payroll and payroll tax expenses represented one officer’s payroll and payroll tax expenses and 10% of payroll and payroll tax expenses paid for Dr. Menon. The Company recorded 90% of payroll paid to Dr. Menon and the related payroll tax expenses under Research and Development Expense.

 

 
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Professional Fees

 

Below is a summary of our Professional fees for the three months ended March 31,September 30, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

 

Three months ended

 

 

Change

 

 

 

March 31,

 

 

2018 vs. 2017

 

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Audit, legal and professional fees

 

$195,000

 

 

 

201,000

 

 

 

(6,000)

 

 

-3

%

 

 

Three months ended

 

 

Change

 

 

 

September 30,

 

 

2019 vs. 2018

 

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Audit, legal and professional fees

 

$259,000

 

 

 

252,000

 

 

 

7,000

 

 

 

3%

 

Professional fees decreasedincreased during the three months ended March 31,September 30, 2018 primarily related to decreaseincrease in legal fees.

 

Other Income (Expense)

 

Below is a summary of our other income (expense) for the three months ended March 31,September 30, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

Three months ended

 

Change

 

 

Three months ended

 

Change

 

 

March 31,

 

2018 vs. 2017

 

 

September 30,

 

2019 vs. 2018

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Interest Income

 

$-

 

-

 

-

 

-

%

 

$-

 

1.000

 

(1,000)

 

(100)%

Interest Expenses

 

 

(51,000)

 

 

(51,000)

 

 

-

 

 

 

-

%

 

 

(51,000)

 

 

(51,000)

 

 

-

 

 

 

-

%

Other Income (Expense), net

 

$(51,000)

 

 

(51,000)

 

 

-

 

 

 

-

%

 

$(51,000)

 

 

(50,000)

 

 

(1,000)

 

 

2%

 

There was noslight change in interest income from bank deposits and there was no change in interest expenses paid on the note payable – related party (see Note 9 to the notes to the condensed financial statements).

 

Net Losses

 

We incurred net losses of $2.4$2.1 million and $3.9$4.5 million for the three months ended March 31, 2018 and 2017, respectively because of the above-mentioned factors.

For the nine months ended March 31, 2018 and 2017

Revenue

We generated no revenue and incurred operating expenses of approximately $11.4 million and $10.1 million for the nine months ended March 31, 2018 and 2017, respectively.

26
Table of Contents

Research and Development Expenses for Proprietary Programs

Below is a summary of our research and development expenses for our proprietary programs by categories of costs for the nine months ended March 31, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

For the nine months ended

 

 

Change

 

 

 

March 31,

 

 

2018 vs. 2017

 

 

 

2018

 

 

2017

 

 

 $

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Clinical studies and development research

 

$6,164,000

 

 

$5,129,000

 

 

$1,035,000

 

 

 

20%

Officers’ payroll and payroll tax expenses related to R&D Department

 

 

615,000

 

 

 

685,000

 

 

 

(70,000

 

 

-10

%

Employees payroll and payroll tax expenses related to R&D Department

 

 

784,000

 

 

 

1,001,000

 

 

 

(217,000

 

 

-22

%

Stock-based compensation - officers

 

 

1,470,000

 

 

 

861,000

 

 

 

609,000

 

 

 

71%

Stock-based compensation - employees

 

 

115,000

 

 

 

110,000

 

 

 

5,000

 

 

 

5%

Stock-based compensation - consultants

 

 

80,000

 

 

 

55,000

 

 

 

25,000

 

 

 

45%

Depreciation and amortization expenses

 

 

316,000

 

 

 

301,000

 

 

 

15,000

 

 

 

5%

Total

 

$9,544,000

 

 

$8,142,000

 

 

$1,402,000

 

 

 

17%

Research and development expenses for proprietary programs increased during the nine months ended March 31, 2018 primarily due to higher spending on our Brilacidin program and Prurisol program.

Officers’ payroll decreased due to the 50% reduction in salary of one officer, which became effective on January 16, 2018. Clinical studies and development expenses may decrease in future reporting periods depending on the Company’s current and future financial liquidity.

Employees payroll and payroll tax expenses decreased during the nine months ended March 31, 2018 related to the decrease in employees during the nine months ended March 31, 2018.

Stock-based compensation - officers increased during the nine months ended March 31, 2018 primarily related to the stock-based compensation given to our President and Chief Medical Officer on September 1, 2017 and the stock and options granted to our President and Chief Medical Officer on June 27, 2016 that became fully vested and expensed due to the completed clinical trial milestones in December, 2017.

Stock-based compensation- employee increased during the nine months ended March 31, 2018 due to the increase in stock awards to employees during the nine months ended March 31, 2018 compared with the same period in 2017.

Stock-based compensation- consultants increased during the nine months ended March 31, 2018 due to granting more stock awards to consultants during the nine months ended March 31, 2018.

Our research and development expenses include costs related to preclinical and clinical trials, outsourced services and consulting, officers’ payroll and related payroll tax expenses, other wages and related payroll tax expenses, stock-based compensation, depreciation and amortization expenses. We manage our proprietary programs based on scientific data and achievement of research plan goals. Our scientists record their time to specific projects when possible; however, many activities occurring simultaneously benefit multiple projects and cannot be readily attributed to a specific project. Accordingly, the accurate assignment of time and costs to a specific project is difficult and may not give a true indication of the actual costs of a particular project. As a result, we do not report costs on an individual program basis.

General and Administrative Expenses

General and administrative expenses consist mainly of compensation and associated fringe benefits not included in cost of research and development expenses for proprietary programs and include other management, business development, accounting, information technology and administration costs, including patent filing and prosecution, recruiting, consulting and professional services, travel and meals, facilities, depreciation and other office expenses.

Below is a summary of our general and administrative expenses for the nine months ended March 31, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

For the nine months ended

 

 

Change

 

 

 

March 31,

 

 

2018 vs. 2017

 

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Insurance and health expense

 

$348,000

 

 

$385,000

 

 

 

(37,000)

 

 

-10

%

Rent and utility expense

 

 

191,000

 

 

 

200,000

 

 

 

(9,000)

 

 

-5

Other G&A

 

 

350,000

 

 

 

452,000

 

 

 

(102,000)

 

 

-23

%

Total

 

$889,000

 

 

 

1,037,000

 

 

 

(148,000)

 

 

-14

%

General and administrative expenses decreased during the nine months ended March 31, 2018 primarily related to decreases in promotion, advertising and office expenses.

27
Table of Contents

Officers’ Payroll and Payroll Tax Expenses

Below is a summary of our Officers’ payroll and payroll tax expenses for nine months ended March 31, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

Nine months ended

 

 

Change

 

 

 

March 31,

 

 

2018 vs. 2017

 

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Officers’ payroll and payroll tax expenses

 

$392,000

 

 

$398,000

 

 

$(6,000)

 

 

-2

%

Officers’ payroll and payroll tax expenses for the Company was decreased during the nine months ended March 31, 2018 and 2017. The officers’ payroll and payroll tax expenses represented one officer’s payroll and payroll tax expenses and 10% of payroll and payroll tax expenses paid for Dr. Menon. The Company recorded 90% of payroll paid to Dr. Menon and the related payroll tax expenses under Research and Development Expense.

Professional Fees

Below is a summary of our Professional fees for the nine months ended March 31, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

Nine months ended

 

 

Change

 

 

 

March 31,

 

 

2018 vs. 2017

 

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Audit, legal and professional fees

 

$525,000

 

 

$562,000

 

 

$(37,000)

 

 

-7

Professional fees decreased during the nine months ended March 31, 2018 primarily related to decrease in legal fees.

Other Income (Expense)

Below is a summary of our other income (expense) for the nine months ended March 31, 2018 and 2017, respectively (rounded to nearest thousand):

 

 

Nine months ended

 

 

Change

 

 

 

March 31,

 

 

2018 vs. 2017

 

 

 

2018

 

 

2017

 

 

$

 

 

%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Interest Income

 

$1,000

 

 

$2,000

 

 

$(1,000)

 

 

-50

%

Interest Expenses

 

 

(152,000)

 

 

(152,000)

 

 

-

 

 

 

-

Other Income (Expense), net

 

$(151,000)

 

$(150,000)

 

$(1,000)

 

 

1%

There was slight decrease in interest income from bank deposits and there was no change in interest expenses paid on the note payable – related party (see Note 9 to the notes to the condensed financial statements).

Net Losses

We incurred net losses of $11.5 million and $10.3 million for the nine months ended March 31,30, 2018 and 2017, respectively because of the above-mentioned factors.

 

 
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Liquidity and Capital Resources

 

Projected Future Working Capital Requirements - Next Twelve12 Months

 

As of March 31,September 30, 2018, we had approximately $1.3$0.3 million in cash compared to $4.1$2.4 million of cash as of June 30, 2017. We have raised approximately $2.0 million from our stock2018. On October 5, 2018, the Company entered into a securities purchase agreement with Aspire Capital from April 1, 2018 to the date of this filing. We have raised approximately $7.8 million fromone multi-family office for the sale of our commonan aggregate of 2,000 shares of the Company’s newly-created Series B 5% convertible preferred stock for aggregate gross proceeds of approximately $2.0 million. An initial closing for the nine months ended March 31,sale of 1,250 shares of preferred stock closed on October 9, 2018, and a subsequent closing for the sale of 750 shares of preferred stock closed on October 12, 2018. Under the securities purchase agreement, the Company also issued to the investors warrants to purchase up to an additional 8,000 shares of preferred stock for an aggregate purchase price of approximately $7.9 million. As the Company cannot be certain the remaining warrants will be exercised, there can be no assurance those funds will be available when needed.

 

We anticipate that future budget expenditures maywill be approximately $12.2$14 million for the next twelve months, including approximately $8.2$9.0 million for clinical activities, supportive research, and drug product development. We will require additional sources of capital during fiscal years 2018 and 2019 in order to meet these budgeted working capital requirements.product. This assessment is based on current estimates and assumptions regarding our clinical development programs and business needs. Actual working capital requirements could differ materially from this above working capital projection. We will presently need

Our ability to significantly reducesuccessfully raise sufficient funds through the sale of equity securities, when needed to meet future budgeted expenditures is uncertain and subject to market conditions generally, the market for our spending oncommon stock, and our clinical development programsability to sell our common stock and other risks. These factors, among others, raise substantial doubt about our ability to continue as a going concern for the next 12 months. If we are unable to meet our obligations, we could be forced to cease all operations, in which event investors may lose their entire investment in the Company. Our financial statements do not haveinclude any adjustments that might result from the adequate financial resources, as of the dateoutcome of this filing,uncertainty. See Note 2 to fully executethe condensed financial statements included elsewhere in this Quarterly Report on Form 10-Q for a further discussion of our clinical programs.liquidity and the conditions and events which raise substantial doubt regarding our ability to continue as a going concern.

 

We are actively engagedThe primary potential source of cash available to us in licensing discussions with global pharmaceutical companies. Successfully securing partnerships would afford the Company access to immediate and potentially recurring sourcesfuture is from the issuances of non-dilutive capital,our equity securities, including upfront fees, milestone-based payments and tiered royalties. There can be no assurance that the Company will be successful in these business development activities.

On September 6, 2017, the Company entered into a $30 millionthrough our common stock purchase agreement with Aspire Capital which replacedFund, LLC (“Aspire Capital”) dated September 6, 2017, and the prior $30 millionexercise of warrants issued under the October 2018 securities purchase agreement. As of date of this report, the conditions for sales under the Aspire Capital purchase agreement are not satisfied and no sales may occur thereunder. In particular, the common stock purchase agreement and provides that upon the termsCompany and Aspire Capital will not affect any sales under the agreement when the closing sales price of our common stock is less than $0.25 per share. In recent months, our common stock has traded below this threshold, and there is substantial uncertainty regarding our continued ability to sell shares under the common stock purchase agreement. In addition, the October 2018 securities purchase agreement prohibits sales under the Aspire Capital purchase agreement through January 10, 2019, with sales thereafter subject to the conditions and limitations set forth therein, Aspire Capitalsatisfaction of certain conditions.

Our current projected average monthly cash flow shortfall is committedanticipated to purchase up to an aggregate of $30.0 millionaverage approximately $700,000 per month for the next 12 months from the date of the Company’s common stock over the 36-month termfiling of the Purchase Agreement. During the period from September 6, 2017this report. We are working to March 31, 2018, the Company has generated proceedsreduce our projected monthly cash flow shortfall and we are currently seeking new sources of approximately $5.7 million under this agreement with Aspire Capital from the sale of approximately 8.7 million shares of its common stock. As of March 31, 2018 the available balance is approximately $24.3 million. Our ability to continuefinancing to fund our additional research and development activities and corporate overheadwork over the next 12 months from the date of this filing. We have the ability to delay incurring certain operating expenses and continue as a going concern has been and continues to be dependent on this stock purchase agreement or similar agreements with Aspire Capital.in the next 12 months, which could reduce our cash flow shortfall, if needed.

 

Our ability to successfully raise sufficient funds through the sale of equity securities, when needed, is subject to many risks and uncertainties and even if we are successful, future equity issuances would result in dilution to our existing stockholders. Our risk factors are described under the heading “Risk Factors”"Risk Factors" in Part I, Item 1A and elsewhere inof our Annual Report on Form 10-K and in other reports we filed with the SEC on September 11, 2017 and in other reports.SEC.

 

We have been successful at raising capital in the past but there can be no assurance that additional capital will be available on terms acceptable to us or in amounts sufficient to meet our needs. In the event thatIf we are unable to raise sufficientgenerate enough working capital from our current or future financing agreement with Aspire Capitalagreements when needed or secure additional sources of funding, from others, we may be required towill significantly reduce our current rate of spending through reductions in staff and delaying, scaling back or stopping certain research and development programs, including the more costly Phase 2 clinical trials and potential future Phase 3 clinical trials on our wholly-owned development programs as these clinical trialsprograms progress into a later stage of development or severely curtail our operations or otherwise impede our ongoing business efforts, or we could be forced to cease operations altogether.development. Insufficient liquidity may also require us to relinquish greater rights to product candidates at an earlier stage of development or on less favorable terms to us and our stockholders than we would otherwise choose in order to obtain up-front license fees needed to fund operations. These liquidity events could prevent us from successfully executing our current operating plan.

$75 Million Shelf Registration Statement

The Company has an effective shelf registration statement on Form S-3, registering the sale of up to $75 million of the Company’s securities. The Company filed the Form S-3 with the SEC on September 11, 2017, which included registering the shares underlying the 2017 $30 million Aspire Capital stock purchase agreement. Pursuant to the instructions to Form S-3, if the Company’s non-affiliate market capitalization as of an applicable measurement time, such as upon the filing of the Company’s Annual Report on Form 10-K, does not equal or exceed $75 million, the Company will be unable to offer and sell securities from its effective shelf registration statement on Form S-3, and the Company will have to use a registration statement for which it is eligible, such as Form S-1, to offer and sell securities.

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Cash Flows

The following table provides information regarding our cash position, cash flows and capital expenditures for the nine months ended March 31, 2018 and 2017 (rounded to nearest thousand):

 

 

Nine Months Ended

 

 

% Change

 

 

 

March 31

 

 

Increase/

 

 

 

2018

 

 

2017

 

 

(Decrease)

 

 

 

 

 

 

 

 

 

 

 

Net cash used in operating activities

 

$(10,362,000)

 

$(7,949,000)

 

 

30%

Net cash used in investing activities

 

 

(108,000)

 

 

(319,000)

 

 

(66)%

Net cash provided by financing activities

 

 

7,665,000

 

 

 

7,571,000

 

 

 

1%

Net decrease in cash

 

$(2,805,000)

 

$(697,000)

 

 

(302)%

Operating activities

The increase in net cash used in operating activities of $2.4 million versus the prior-year nine-month period was mainly due to increase in our losses from operations of $1.2 million as adjusted for the changes in our working capital accounts.

Investing activities

The decrease in net cash used in investing activities of $0.2 million versus the prior-year nine-month period was mainly due to decrease in purchases of patents of $0.2 million.

During the nine months ended March 31, 2018, our investing activities used cash of $0.1 million, mainly including the purchases of patents of $0.1 million.

During the nine months ended March 31, 2017, our investing activities used cash of $0.3 million, mainly including the purchases of patents of $0.3 million.

Financing activities

The increase in net cash provided by financing activities of approximately $0.1 million versus the prior-year nine-month period was due to an increase in sales of shares of our common stock to Aspire Capital.

During the nine months ended March 31, 2018, we raised approximately $7.8 million in net cash proceeds from the sale of 11.3 million shares of our common stock to Aspire Capital offset by cash paid to taxing authorities arising from the withholding of shares from employees of $172,000.

During the nine months ended March 31, 2017, we raised approximately $7.6 million in net cash proceeds, including $5.4 million in net proceeds from the sale of 5.3 million shares of our common stock to Aspire and $2.2 million in net proceeds from the sale of 2.5 million shares of our common stock at $0.89 per share in a registered direct offering, without an underwriter or placement agent on March 28, 2017.

Requirement for Additional Working Capital

The Company plans to incur total expenses of approximately $12.2 million for the next twelve months, including approximately $8.2 million for clinical activities, supportive research, and drug product development. The Company has limited experience with pharmaceutical drug development. As such, the budget estimate may not be accurate. In addition, the actual work to be performed is not known at this time, other than a broad outline, as is normal with any scientific work. As further work is performed, additional work may become necessary or a change in plans or workload may occur. Such changes may have an adverse impact on our estimated budget and on our projected timeline of drug development.

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The Company will be unable to proceed with its planned drug development programs, meet its administrative expense requirements, capital costs, or staffing costs if it is not successful with its business development efforts or without accessing its financing available with Aspire Capital of approximately $24.3 million as of March 31, 2018. Management has put in place this new 2017 stock purchase agreement with Aspire Capital to fund its future clinical trial expenses and overhead expenses over the next twelve months. This purchase agreement provides that, upon the terms and subject to the conditions and limitations set forth therein, Aspire Capital is committed to purchase up to an aggregate of $30.0 million of the Company’s common stock over the 36-month term of the Purchase Agreement. Management believes, as of the date of this filing that the funding amount from Aspire Capital will be available as needed by the Company. Adverse market conditions in the Company’s per share price of its common stock and its trading volume may prevent the Company from funding its working capital requirements as needed.

 

In the event that we are unable to generate sufficient cash from our Aspire Capital purchase agreementPurchase Agreement or raise additional funds from others, we willmay be required to delay, reduce or severely curtail our operations or otherwise impede our on-going business efforts, which could have a material adverse effect on our future business, operating results, financial condition and long-term prospects. The Company expectsexpect to seek to obtain additional funding through business development activities (i.e. licensing and partnerships) and future equity issuances. There can be no assurance as to the availability or terms upon which such financing and capital might be availableavailable. The accompanying condensed financial statements do not include any adjustments related to us.the carrying values and classifications of assets and liabilities that would be necessary should the Company be unable to continue as a going concern.

  

Contractual Obligations
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Below is$75 Million Shelf Registration Statement

The Company has an effective shelf registration statement on Form S-3, registering the sale of up to $75 million of the Company’s securities. The Company filed with the Securities and Exchange Commission (i) a prospectus supplement, dated November 13, 2017, registering up to $30 million of our common stock that have been or may be offered and sold to Aspire Capital from time to time, (ii) a prospectus supplement, dated June 28, 2018, registering $7.0 million of our common stock and warrants to purchase 8.0 million shares of our common stock in a registered direct offering, and (iii) a prospectus supplement, dated October 5, 2018, registering $10.0 million of our preferred stock, warrants to purchase preferred stock, and underlying shares of our common stock in a registered direct offering, leaving approximately $23 million available under the Company’s effective shelf registration statement. Depending on the Company’s public float, the Company may not be eligible to utilize Form S-3 for future primary offerings of its securities following the filing of its Annual Reports on Form 10-K in 2019 and 2020. The Company anticipates that in the future, if it were to no longer eligible to use Form S-3, that it may utilize Form S-1 to register the sale of its securities, including through future financing agreements with Aspire Capital.

Cash Flows

The following table that presentsprovides information regarding our contractual obligationscash position, cash flows and commercial commitments as of March 31,capital expenditures for the three months ended September 30, 2018 and 2017 (rounded to the nearest million)thousand):

 

 

 

Payments Due by Period

 

 

 

Total

 

 

Less than One Year

 

 

2 Year

 

 

3-5 Years

 

 

More than 5 Years

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

CRO obligations (1)

 

$1.0

 

 

$1.0

 

 

$-

 

 

$-

 

 

$-

 

Lease obligations (2)

 

$0.2

 

 

$0.1

 

 

$0.1

 

 

$-

 

 

$-

 

Total

 

$1.2

 

 

$1.1

 

 

$0.1

 

 

$-

 

 

$-

 

___________ 

(1)

The Company has contractual minimum commitments to Contract Research Organizations of $1.0 million as of March 31, 2018.

(2)

The Company signed a lease extension agreement with Cummings Properties which began on October 1, 2013. The lease is for a term of five years ending on September 30, 2018, and requires monthly payments of approximately $18,000. The Company will receive $900 per month from the sublease of 200 square feet of space to Innovative Medical Research Inc., a company owned by Leo Ehrlich and Dr. Krishna Menon, officers of our Company, which is not included in the table above.

 

 

Three Months Ended

 

 

Change

 

 

 

September 30,

 

 

Increase/

 

 

 

2018

 

 

2017

 

 

(Decrease)

 

 

 

 

 

 

 

 

 

%

 

Net cash used in operating activities

 

$(2,099,000)

 

$(3,689,000)

 

 

(43)%

Net cash used in investing activities

 

 

(19,000)

 

 

(22,000)

 

 

(14)%

Net cash provided by financing activities

 

 

-

 

 

 

2,503,000

 

 

 

(100)%

Net decrease in cash

 

$(2,118,000)

 

$(1,208,000)

 

 

75%

 

Equity TransactionsThe decrease in net cash used in operating activities of $1.6 million versus the prior-year three-month period was mainly due to decreases in our losses from operations of $2.4 million, largely attributable to our less spending for research and development expenses.

 

From April 1,Our operating activities used cash of $2.1 million and $3.7 million for the three months ended September 30, 2018 and 2017, respectively. The use of cash in these periods principally resulted from our losses from operations, as adjusted for non-cash charges for stock-based compensation, amortization and depreciation, and changes in our working capital accounts.

Investing activities

The decrease in net cash used in investing activities versus the prior-year three-month period was due to May 6,a decrease in patents costs.

Financing activities

During the three months ended September 30, 2018, we did not have any financing activity. During the Company has generated additionalthree months ended September 30, 2017, we raised approximately $2.5 million in net cash proceeds of approximately $2.0 million under the Common Stock Purchase Agreement with Aspire Capital from the sale of approximately 8.03.2 million shares of itsour common stock.stock to Aspire Capital. 

 

Off-Balance Sheet Arrangements

 

The Company does not have any off-balance sheet arrangements, as defined in Item 304(a)(4)(ii) of Regulation S-K.S-K under the Securities Exchange Act of 1934, as amended.

 

 
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ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

 

The Company maintains an investment portfolio in accordance with our investment policy. The primary objectives of our investment policy are to preserve principal, maintain proper liquidity to meet operating needs and maximize yields. The Company holds investments that are subject to credit risk, but not interest rate risks. The Company does not own derivative financial instruments in our investment portfolio. Accordingly, the Company does not believe there is any material market risk exposure that would require disclosure under this item.Not applicable.

 

ITEM 4. CONTROLS AND PROCEDURES

 

Evaluation of Disclosure Controls and Procedures

 

We have established disclosure controls and procedures to ensure that the information required to be disclosed by the Company in the reports that it files or submits under the Securities Exchange Act of 1934, as amended (the “Exchange Act”), is recorded, processed, summarized and reported within the time periods specified in SEC rules and forms and that such information is accumulated and communicated to management, including our principal executive officer and principal financial officer, as appropriate to allow timely decisions regarding required disclosure.

 

As of March 31,September 30, 2018, management, with the participation of our principal executive officer and principal financial officer, carried out an evaluation of the effectiveness of the design and operation of the Company’s disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) of the Exchange Act). Based on such evaluation, as of March 31,September 30, 2018, the principal executive officer and principal financial officer of the Company have concluded that the Company’s disclosure controls and procedures are effective.

 

Changes in Internal Controls

 

There have been no changes in our internal control over financial reporting during the quarter ended March 31,September 30, 2018, that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

 

Limitations on Effectiveness of Controls and Procedures

 

In designing and evaluating the disclosure controls and procedures, management recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired control objectives. In addition, the design of disclosure controls and procedures must reflect the fact that there are resource constraints and that management is required to apply its judgment in evaluating the benefits of possible controls and procedures relative to their costs.

 

 
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PART II. OTHER INFORMATION

 

ITEM 1. LEGAL PROCEEDINGS

 

None

 

ITEM 1A. RISK FACTORS

 

Our operations and financial results are subject to various risks and uncertainties, including those described in Part I, Item 1A, “Risk Factors” in our Annual Report on Form 10-K for the year ended June 30, 2017,2018, which could adversely affect our business, financial condition, results of operations, cash flows, and the trading price of our common and capital stock. There have been no material changes to our risk factors since our Annual Report on Form 10-K for the year ended June 30, 2017.2018.

 

ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES

 

None

 

ITEM 3. DEFAULTS UPON SENIOR SECURITIES

 

None

 

ITEM 4. MINE SAFETY DISCLOSURES

 

None

 

ITEM 5. OTHER INFORMATION

 

None

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ITEM 6. EXHIBITS

 

(a) Exhibit index

 

(1)The documents set forth below are filed herewith or incorporated herein by reference to the location indicated.

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(1) The documents set forth below are filed herewith or incorporated herein by reference to the location indicated. 

  

EXHIBIT INDEX

 

Exhibit No.

 

Title

 

Method of Filing

 

31.1

 

President of Researchand Chief Medical Officer Certifications required under Section 302 of the Sarbanes Oxley Act of 2002

 

Filed herewith

 

31.2

 

Chief Executive Officer and Chief Financial Officer Certifications required under Section 302 of the Sarbanes Oxley Act of 2002

 

Filed herewith

 

32.1

 

President of Researchand Chief Medical Officer Certifications required under Section 906 of the Sarbanes Oxley Act of 2002

 

Furnished herewith

 

32.2

 

Chief Executive Officer and Chief Financial Officer Certifications required under Section 906 of the Sarbanes Oxley Act of 2002

 

Furnished herewith

 

101

 

The following materials from the Company’s Quarterly Report on Form 10-Q for the ninethree months ended March 31,September 30, 2018 formatted in Extensible Business Reporting Language (XBRL): (i) the Condensed Statements of Income, (ii) the Condensed Statements of Comprehensive Income, (iii) the Condensed Balance Sheets, (iv) the Condensed Statements of Cash Flows, and (v) related notes

 

Filed herewith

 

 
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SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

 

INNOVATION PHARMACEUTICALS INC.

 

Dated: May 10,November 8, 2018

By:

/s/ Leo Ehrlich

Name:

Leo Ehrlich

Title:

Chief Executive Officer and Chief Financial Officer

(Principal Executive, Accounting and Financial Officer)

 

Dated: November 8, 2018

By:

/s/ Krishna MenonArthur P. Bertolino

Name:

Arthur P. Bertolino

 

Krishna Menon

Title:

President of Researchand Chief Medical Officer

 

 

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