Table of Contents
UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-Q

(Mark One)

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

For the quarterly period ended September 30, 2019

2020

OR

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:  0-26642

MYRIAD GENETICS, INC.

(Exact name of registrant as specified in its charter)

Delaware
(State or other jurisdiction
of incorporation or organization)
320 Wakara Way, Salt Lake City, UT
(Address of principal executive offices)
87-0494517
(I.R.S. Employer Identification No.)

84108
(Zip Code)
Delaware

87-0494517

(State or other jurisdiction

of incorporation or organization)

(I.R.S. Employer Identification No.)

320 Wakara Way, Salt Lake City, UT

84108

(Address of principal executive offices)

(Zip Code)

Registrant's telephone number, including area code: (801) 584-3600

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

Trading


Symbol(s)

Name of each exchange on which registered

Public Common Stock, $0.01 par value

MYGN

Nasdaq Global Select Market

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 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 every Interactive Data File required to be submitted 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 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

x

Accelerated filer

Non-accelerated filer

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. ¨

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

Indicate by check mark whether the registrant has filed all documents and reports required to be filed by Sections 12, 13 or 15(d) of the Securities Exchange Act of 1934 subsequent to the distribution of securities under a plan confirmed by a court.     Yes      No  

As of November 4, 20192, 2020, the registrant had 74,389,02475,210,480 shares of $0.01 par value common stock outstanding.


MYRIAD GENETICS, INC.

INDEX TO FORM 10-Q




Table of Contents
MYRIAD GENETICS, INC.
INDEX TO FORM 10-Q

Page

Page

23

28

28

29

29

30

30


2


Table of Contents


MYRIAD GENETICS, INC.

AND SUBSIDIARIES

Condensed Consolidated Balance Sheets (Unaudited)

(In millions)

 

September 30,

 

 

June 30,

 

ASSETS

 

2019

 

 

2019

 

ASSETSSeptember 30,
2020
June 30,
2020
(Unaudited)

Current assets:

 

 

 

 

 

 

 

 

Current assets:

Cash and cash equivalents

 

$

89.9

 

 

$

93.2

 

Cash and cash equivalents$118.3 $163.7 

Marketable investment securities

 

 

52.7

 

 

 

43.7

 

Marketable investment securities42.1 54.1 

Prepaid expenses

 

 

14.0

 

 

 

16.6

 

Prepaid expenses12.5 13.8 

Inventory

 

 

28.1

 

 

 

31.4

 

Inventory26.6 29.1 

Trade accounts receivable

 

 

117.0

 

 

 

133.9

 

Trade accounts receivable85.1 68.1 

Prepaid taxes

 

 

23.0

 

 

 

25.1

 

Prepaid taxes107.9 

Other receivables

 

 

4.8

 

 

 

4.7

 

Other receivables2.0 2.9 

Total current assets

 

 

329.5

 

 

 

348.6

 

Total current assets394.5 331.7 

Property, plant and equipment, net

 

 

55.0

 

 

 

57.3

 

Property, plant and equipment, net36.7 37.0 

Operating lease right-of-use assets

 

 

71.3

 

 

 

 

Operating lease right-of-use assets62.7 66.0 

Long-term marketable investment securities

 

 

51.5

 

 

 

54.9

 

Long-term marketable investment securities30.2 37.0 

Intangibles, net

 

 

667.8

 

 

 

684.7

 

Intangibles, net590.9 605.3 

Goodwill

 

 

416.1

 

 

 

417.2

 

Goodwill328.3 327.6 
Other assetsOther assets1.2 

Total assets

 

$

1,591.2

 

 

$

1,562.7

 

Total assets$1,444.5 $1,404.6 

LIABILITIES AND STOCKHOLDERS' EQUITY

 

 

 

 

 

 

 

 

LIABILITIES AND STOCKHOLDERS' EQUITY

Current liabilities:

 

 

 

 

 

 

 

 

Current liabilities:

Accounts payable

 

$

24.0

 

 

$

33.3

 

Accounts payable$19.1 $21.7 

Accrued liabilities

 

 

73.0

 

 

 

78.9

 

Accrued liabilities65.4 75.9 

Current maturities of operating lease liabilities

 

 

13.0

 

 

 

 

Current maturities of operating lease liabilities13.6 13.5 

Short-term contingent consideration

 

 

3.3

 

 

 

3.4

 

Short-term contingent consideration3.3 3.1 

Deferred revenue

 

 

2.1

 

 

 

2.2

 

Deferred revenue32.3 32.8 

Total current liabilities

 

 

115.4

 

 

 

117.8

 

Total current liabilities133.7 147.0 

Unrecognized tax benefits

 

 

22.1

 

 

 

21.7

 

Unrecognized tax benefits37.4 23.5 
Long-term deferred taxesLong-term deferred taxes75.3 26.6 
Long-term debtLong-term debt224.6 224.4 

Noncurrent operating lease liabilities

 

 

62.6

 

 

 

 

Noncurrent operating lease liabilities53.5 56.9 

Other long-term liabilities

 

 

7.3

 

 

 

7.8

 

Other long-term liabilities10.7 8.0 

Contingent consideration

 

 

7.4

 

 

 

10.4

 

Long-term debt

 

 

225.0

 

 

 

233.5

 

Long-term deferred taxes

 

 

76.9

 

 

 

82.6

 

Total liabilities

 

 

516.7

 

 

 

473.8

 

Total liabilities535.2 486.4 

Commitments and contingencies

 

 

 

 

 

 

 

 

Commitments and contingencies

Stockholders’ equity:

 

 

 

 

 

 

 

 

Stockholders’ equity:

Common stock, 74.4 and 73.5 shares outstanding at September 30, 2019 and

June 30, 2019 respectively

 

 

0.7

 

 

 

0.7

 

Common stock, 75.2 and 74.7 shares outstanding at September 30, 2020 and June 30, 2020 respectivelyCommon stock, 75.2 and 74.7 shares outstanding at September 30, 2020 and June 30, 2020 respectively0.8 0.7 

Additional paid-in capital

 

 

1,076.3

 

 

 

1,068.0

 

Additional paid-in capital1,101.2 1,096.6 

Accumulated other comprehensive loss

 

 

(7.5

)

 

 

(5.4

)

Accumulated other comprehensive loss(3.6)(5.2)

Retained earnings

 

 

5.0

 

 

 

25.6

 

Accumulated deficitAccumulated deficit(189.1)(173.9)

Total Myriad Genetics, Inc. stockholders’ equity

 

 

1,074.5

 

 

 

1,088.9

 

Total Myriad Genetics, Inc. stockholders’ equity909.3 918.2 

Non-Controlling Interest

 

 

 

 

 

 

Non-controlling interestNon-controlling interest

Total stockholders' equity

 

 

1,074.5

 

 

 

1,088.9

 

Total stockholders' equity909.3 918.2 

Total liabilities and stockholders’ equity

 

$

1,591.2

 

 

$

1,562.7

 

Total liabilities and stockholders’ equity$1,444.5 $1,404.6 

See accompanying notes to condensed consolidated financial statements.

3


Table of Contents
MYRIAD GENETICS, INC.

AND SUBSIDIARIES

Condensed Consolidated Statements of Operations (Unaudited)

(In millions, except per share amounts)

 

Three months ended

 

 

September 30,

 

Three months ended
September 30,

 

2019

 

 

2018

 

20202019

Molecular diagnostic testing

 

$

172.0

 

 

$

189.0

 

Molecular diagnostic testing$135.7 $172.0 

Pharmaceutical and clinical services

 

 

14.3

 

 

 

13.3

 

Pharmaceutical and clinical services9.5 14.3 

Total revenue

 

 

186.3

 

 

 

202.3

 

Total revenue145.2 186.3 

Costs and expenses:

 

 

 

 

 

 

 

 

Costs and expenses:

Cost of molecular diagnostic testing

 

 

41.2

 

 

 

42.3

 

Cost of molecular diagnostic testing39.9 41.2 

Cost of pharmaceutical and clinical services

 

 

8.5

 

 

 

7.4

 

Cost of pharmaceutical and clinical services4.3 8.5 

Research and development expense

 

 

21.3

 

 

 

21.1

 

Research and development expense17.6 21.3 

Change in the fair value of contingent consideration

 

 

0.7

 

 

 

0.4

 

Change in the fair value of contingent consideration(1.1)0.7 

Selling, general, and administrative expense

 

 

135.5

 

 

 

129.9

 

Selling, general, and administrative expense124.1 135.5 

Total costs and expenses

 

 

207.2

 

 

 

201.1

 

Total costs and expenses184.8 207.2 

Operating income (loss)

 

 

(20.9

)

 

 

1.2

 

Operating lossOperating loss(39.6)(20.9)

Other income (expense):

 

 

 

 

 

 

 

 

Other income (expense):

Interest income

 

 

0.9

 

 

 

0.7

 

Interest income0.4 0.9 

Interest expense

 

 

(2.9

)

 

 

(2.2

)

Interest expense(2.9)(2.9)

Other

 

 

0.6

 

 

 

1.1

 

Other(1.6)0.6 

Total other expense:

 

 

(1.4

)

 

 

(0.4

)

Income (loss) before income tax

 

 

(22.3

)

 

 

0.8

 

Income tax provision (benefit)

 

 

(1.7

)

 

 

1.6

 

Net income (loss)

 

$

(20.6

)

 

$

(0.8

)

Total other expense, netTotal other expense, net(4.1)(1.4)
Loss before income taxLoss before income tax(43.7)(22.3)
Income tax benefitIncome tax benefit(28.5)(1.7)
Net lossNet loss(15.2)(20.6)

Net loss attributable to non-controlling interest

 

 

 

 

 

(0.1

)

Net loss attributable to non-controlling interest

Net income (loss) attributable to Myriad Genetics, Inc. stockholders

 

$

(20.6

)

 

$

(0.7

)

Earnings (loss) per share:

 

 

 

 

 

 

 

 

Basic

 

$

(0.28

)

 

$

(0.01

)

Diluted

 

$

(0.28

)

 

$

(0.01

)

Net loss attributable to Myriad Genetics, Inc. stockholdersNet loss attributable to Myriad Genetics, Inc. stockholders$(15.2)$(20.6)
Net loss per share:Net loss per share:
Basic and dilutedBasic and diluted$(0.20)$(0.28)

Weighted average shares outstanding:

 

 

 

 

 

 

 

 

Weighted average shares outstanding:

Basic

 

 

73.7

 

 

 

73.0

 

Diluted

 

 

73.7

 

 

 

73.0

 

Basic and dilutedBasic and diluted74.7 73.7 

See accompanying notes to condensed consolidated financial statements.

4


Table of Contents
MYRIAD GENETICS, INC.

AND SUBSIDIARIES

Condensed Consolidated Statements of Comprehensive IncomeLoss (Unaudited)

(In millions)

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Net income (loss) attributable to Myriad Genetics, Inc. stockholders

 

$

(20.6

)

 

$

(0.7

)

Unrealized gain (loss) on available-for-sale securities, net of tax

 

 

 

 

 

(0.2

)

Change in foreign currency translation adjustment, net of tax

 

 

(2.2

)

 

 

0.4

 

Comprehensive income (loss)

 

 

(22.8

)

 

 

(0.5

)

Comprehensive income attributable to non-controlling interest

 

 

 

 

 

 

Comprehensive income (loss) attributable to Myriad Genetics, Inc.

   shareholders

 

$

(22.8

)

 

$

(0.5

)

Three months ended
September 30,
20202019
Net loss attributable to Myriad Genetics, Inc. stockholders$(15.2)$(20.6)
Unrealized loss on available-for-sale debt securities, net of tax(0.2)
Change in foreign currency translation adjustment, net of tax1.8 (2.2)
Comprehensive loss(13.6)(22.8)
Comprehensive loss attributable to non-controlling interest
Comprehensive loss attributable to Myriad Genetics, Inc. shareholders$(13.6)$(22.8)

See accompanying notes to condensed consolidated financial statements.

5


Table of Contents
MYRIAD GENETICS, INC.

AND SUBSIDIARIES

Condensed Consolidated Statements of Stockholders’ Equity

(In millions)

 

 

 

 

 

 

 

 

 

 

Accumulated

 

 

Retained

 

 

Myriad

 

 

 

 

 

 

 

Additional

 

 

other

 

 

earnings

 

 

Genetics, Inc.

 

 

 

Common

 

 

paid-in

 

 

comprehensive

 

 

(accumulated

 

 

Stockholders’

 

 

 

stock

 

 

capital

 

 

loss

 

 

deficit)

 

 

equity

 

BALANCES AT JUNE 30, 2018

 

$

0.7

 

 

$

915.4

 

 

$

(4.1

)

 

$

54.1

 

 

$

966.1

 

Issuance of common stock under share-based compensation plans

 

 

 

 

 

1.9

 

 

 

 

 

 

 

 

 

1.9

 

Share-based payment expense

 

 

 

 

 

127.4

 

 

 

 

 

 

 

 

 

127.4

 

Repurchase and retirement of common stock

 

 

 

 

 

7.7

 

 

 

 

 

 

 

 

 

7.7

 

Net income

 

 

 

 

 

 

 

 

 

 

 

(0.7

)

 

 

(0.7

)

Other comprehensive income, net of tax

 

 

 

 

 

 

 

 

(0.2

)

 

 

 

 

 

(0.2

)

BALANCES AT SEPTEMBER 30, 2018

 

$

0.7

 

 

$

1,052.4

 

 

$

(4.3

)

 

$

53.4

 

 

$

1,102.2

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

BALANCES AT JUNE 30, 2019

 

$

0.7

 

 

$

1,068.0

 

 

$

(5.4

)

 

$

25.6

 

 

$

1,088.9

 

Issuance of common stock under share-based

   compensation plans

 

 

 

 

 

(0.5

)

 

 

 

 

 

 

 

 

(0.5

)

Share-based payment expense

 

 

 

 

 

8.8

 

 

 

 

 

 

 

 

 

8.8

 

Net income (loss)

 

 

 

 

 

 

 

 

 

 

 

(20.6

)

 

 

(20.6

)

Other comprehensive income, net of tax

 

 

 

 

 

 

 

 

(2.1

)

 

 

 

 

 

(2.1

)

BALANCES AT SEPTEMBER 30, 2019

 

$

0.7

 

 

$

1,076.3

 

 

$

(7.5

)

 

$

5.0

 

 

$

1,074.5

 

Common
stock
Additional
paid-in
capital
Accumulated
other
comprehensive
loss
Retained
earnings
(accumulated
deficit)
Myriad
Genetics, Inc.
Stockholders’
equity
BALANCES AT JUNE 30, 2019$0.7 $1,068.0 $(5.4)$25.6 $1,088.9 
Issuance of common stock under share-based compensation plans, net of shares exchanged for withholding tax— (0.5)— — (0.5)
Share-based payment expense— 8.8 — — 8.8 
Net loss— — — (20.6)(20.6)
Other comprehensive loss, net of tax— — (2.1)— (2.1)
BALANCES AT SEPTEMBER 30, 2019$0.7 $1,076.3 $(7.5)$5.0 $1,074.5 
BALANCES AT JUNE 30, 2020$0.7 $1,096.6 $(5.2)$(173.9)$918.2 
Issuance of common stock under share-based compensation plans, net of shares exchanged for withholding tax0.1 (3.8)— — (3.7)
Share-based payment expense— 8.4 — — 8.4 
Net loss— — — (15.2)(15.2)
Other comprehensive income, net of tax— — 1.6 — 1.6 
BALANCES AT SEPTEMBER 30, 2020$0.8 $1,101.2 $(3.6)$(189.1)$909.3 

See accompanying notes to consolidated financial statements.

6


Table of Contents
MYRIAD GENETICS, INC.

AND SUBSIDIARIES

Condensed Consolidated Statements of Cash Flows (Unaudited)

(In millions)

 

Three months ended

 

 

September 30,

 

Three months ended
September 30,

 

2019

 

 

2018

 

20202019

CASH FLOWS FROM OPERATING ACTIVITIES:

 

 

 

 

 

 

 

 

CASH FLOWS FROM OPERATING ACTIVITIES:

Net Income (loss) attributable to Myriad Genetics, Inc. stockholders

 

$

(20.6

)

 

 

(0.7

)

Adjustments to reconcile net income to net cash provided by operating activities:

 

 

 

 

 

 

 

 

Net loss attributable to Myriad Genetics, Inc. stockholdersNet loss attributable to Myriad Genetics, Inc. stockholders$(15.2)$(20.6)
Adjustments to reconcile net loss to net cash provided by operating activities:Adjustments to reconcile net loss to net cash provided by operating activities:

Depreciation and amortization

 

 

18.2

 

 

 

18.3

 

Depreciation and amortization17.7 18.2 

Non-cash interest expense

 

 

0.1

 

 

 

(1.3

)

Non-cash interest expense0.2 0.1 
Non-cash lease expenseNon-cash lease expense3.3 3.2 

Loss (gain) on disposition of assets

 

 

(0.1

)

 

 

(1.0

)

Loss (gain) on disposition of assets0.1 (0.1)

Share-based compensation expense

 

 

8.8

 

 

 

7.7

 

Share-based compensation expense8.4 8.8 

Deferred income taxes

 

 

(5.1

)

 

 

2.7

 

Deferred income taxes48.4 (5.1)

Unrecognized tax benefits

 

 

0.4

 

 

 

(2.6

)

Unrecognized tax benefits13.9 0.4 

Change in fair value of contingent consideration

 

 

0.7

 

 

 

(0.4

)

Change in fair value of contingent consideration(1.1)0.7 

Changes in assets and liabilities:

 

 

 

 

 

 

 

 

Changes in assets and liabilities:

Prepaid expenses

 

 

2.6

 

 

 

1.8

 

Prepaid expenses1.2 2.6 

Trade accounts receivable

 

 

16.7

 

 

 

(3.3

)

Trade accounts receivable(17.0)16.7 

Other receivables

 

 

(0.1

)

 

 

(0.3

)

Other receivables0.9 (0.1)

Inventory

 

 

3.1

 

 

 

3.5

 

Inventory2.6 3.1 

Prepaid taxes

 

 

2.1

 

 

 

(3.6

)

Prepaid taxes(107.9)2.1 
Other assetsOther assets(1.2)

Accounts payable

 

 

(9.3

)

 

 

(8.4

)

Accounts payable(3.2)(9.3)

Accrued liabilities

 

 

(1.7

)

 

 

(4.4

)

Accrued liabilities(9.8)(4.9)

Deferred revenue

 

 

 

 

 

(0.2

)

Deferred revenue(0.6)

Net cash provided by operating activities

 

 

15.8

 

 

 

7.8

 

Net cash (used in) provided by operating activitiesNet cash (used in) provided by operating activities(59.3)15.8 

CASH FLOWS FROM INVESTING ACTIVITIES

 

 

 

 

 

 

 

 

CASH FLOWS FROM INVESTING ACTIVITIES

Capital expenditures

 

 

(1.4

)

 

 

(1.3

)

Capital expenditures(1.5)(1.4)

Acquisitions, net of cash acquired

 

 

 

 

 

(279.6

)

Purchases of marketable investment securities

 

 

(23.1

)

 

 

(14.4

)

Purchases of marketable investment securities(23.1)

Proceeds from maturities and sales of marketable investment securities

 

 

17.4

 

 

 

16.3

 

Proceeds from maturities and sales of marketable investment securities18.6 17.4 

Net cash used in investing activities

 

 

(7.1

)

 

 

(279.0

)

Net cash provided by (used in) investing activitiesNet cash provided by (used in) investing activities17.1 (7.1)

CASH FLOWS FROM FINANCING ACTIVITIES:

��

 

 

 

 

 

 

 

CASH FLOWS FROM FINANCING ACTIVITIES:

Net proceeds from common stock issued under share-based compensation plans

 

 

(0.4

)

 

 

2.1

 

Payment for tax withholding for common stock issued under share-based compensation plansPayment for tax withholding for common stock issued under share-based compensation plans(3.8)(0.4)

Payment of contingent consideration recognized at acquisition

 

 

(3.3

)

 

 

 

Payment of contingent consideration recognized at acquisition(0.1)(3.3)

Net proceeds from revolving credit facility

 

 

 

 

 

290.0

 

Repayment of revolving credit facility

 

 

(8.6

)

 

 

(40.0

)

Repayment of revolving credit facility(8.6)

Net cash provided by (used in) financing activities

 

 

(12.3

)

 

 

252.1

 

Net cash used in financing activitiesNet cash used in financing activities(3.9)(12.3)

Effect of foreign exchange rates on cash and cash equivalents

 

 

0.3

 

 

 

1.5

 

Effect of foreign exchange rates on cash and cash equivalents0.7 0.3 

Net decrease in cash and cash equivalents

 

 

(3.3

)

 

 

(17.6

)

Net decrease in cash and cash equivalents(45.4)(3.3)

Cash and cash equivalents at beginning of the period

 

 

93.2

 

 

 

110.9

 

Cash and cash equivalents at beginning of the period163.7 93.2 

Cash and cash equivalents at end of the period

 

$

89.9

 

 

$

93.3

 

Cash and cash equivalents at end of the period$118.3 $89.9 

See accompanying notes to condensed consolidated financial statements.

7


Table of Contents
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED)

(Dollars and shares in millions, except per share data)

(1)

BASIS OF PRESENTATION

(1)BASIS OF PRESENTATION
The accompanying condensed consolidated financial statements have been prepared byfor Myriad Genetics, Inc. and subsidiaries (the “Company” or “Myriad”) have been prepared in accordance with U.S. generally accepted accounting principles (“GAAP”) for interim financial information and pursuant to the applicable rules and regulations of the Securities and Exchange Commission (“SEC”). The condensed consolidated financial statements include the accounts of the Company and its wholly owned subsidiaries.  All intercompany accounts and transactions have been eliminated in consolidation. In the opinion of management, the accompanying financial statements contain all adjustments (consisting of normal and recurring accruals) necessary to present fairly all financial statements in accordance with GAAP. The condensed consolidated financial statements herein should be read in conjunction with the Company’s audited consolidated financial statements and notes thereto for the fiscal year ended June 30, 2019, included in the Company’s Annual Report on Form 10-K for the fiscal year ended June 30, 2019. Operating results for the three months ended September 30, 2019 may not necessarily be indicative of results to be expected for any other interim period or for the full year.

The consolidated financial statements include the accounts of the Company’s majority-owned subsidiary, Assurex Canada, Ltd. which is 85% owned by Assurex Health, Inc. (“Assurex”), a wholly owned subsidiary of the Company, and 15% owned by the Centre for Addiction and Mental Health. Assurex Canada, Ltd. is a consolidated subsidiary of Assurex Health, Inc. The value of the non-controlling interest represents the portion of Assurex Canada, Ltd.’s profit or loss and net assets that is not held by Assurex Health, Inc. The Company attributes comprehensive income or loss of the subsidiary between the Company and the non-controlling interest based on the respective ownership interest.

2020.

The preparation of financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosures of contingent assets and liabilities at the date of the financial statements, as well as the reported amounts of revenue and expenses during the reporting period. ActualOperating results could differ from those estimates.

Recent Accounting Pronouncements

Recently Adopted Standards

In February 2016, the FASB issued ASU 2016-02, Leases (“ASU 2016-02”). ASU 2016-02 amends the existing accounting standards for lease accounting, including requiring lessees to recognize most leases on their balance sheets and changing certain lessor accounting requirements. ASU 2016-02 also requires entities to provide enhanced disclosures surrounding the amount, timing and uncertainty of cash flows arising from leasing arrangements. On July 1, 2019, the Company adopted ASU 2016-02 under the modified retrospective approach by initially applying ASU 2016-02 at the adoption date, rather than at the beginning of the earliest comparative period presented. Results for the three months ended September 30, 2019 are presented under ASU 2016-02. Prior2020 may not necessarily be indicative of results to be expected for any other interim period or for the full year.

The full impact of the COVID-19 outbreak continues to evolve and its future impact remains highly uncertain and unpredictable. As such, it is uncertain as to the full magnitude of the effect that the pandemic will have on the Company's financial condition, liquidity, and future results of operations. Management is actively monitoring the impact of the global situation on the Company's financial condition, liquidity, operations, suppliers, industry, and workforce. Given the daily evaluation of the COVID-19 outbreak and the global responses to curb its spread, the Company is not able to estimate the effects of the COVID-19 outbreak on its results of operations, financial condition, or liquidity for future periods.
We have historically experienced seasonality in our testing business. The volume of testing is negatively impacted by the summer season, which is generally reflected in the quarter ended June 30. The quarter ending December 31 is generally strong as we see an increase in volumes from patients who have met their annual insurance deductible. Conversely, the quarter ending March 31 is typically negatively impacted by the annual reset of patient deductibles. Due to the global pandemic, we cannot predict if seasonality will follow the same pattern as in prior years.
Reclassifications
Certain prior period amounts were not adjusted and continuehave been reclassified to be reported under previous lease accounting guidance.

Under ASU 2016-02,conform with the Company determines if an arrangement iscurrent period presentation. The reclassifications have no impact on the total assets, total liabilities, stockholders’ equity, cash flows from operations, or contains a lease at inception by assessing whether the arrangement contains an identified asset and whether it has the right to control the identified asset. Right-of-use (“ROU”) assets represent the Company's right to use an underlying assetnet loss for the lease term and lease liabilities represent the Company's obligation to make lease payments arising from the lease. Lease liabilities are recognized at the lease commencement date based on the present value of future lease payments over the lease term. ROU assets are based on the measurement of the lease liability and also include any lease payments made prior to or on lease commencement and exclude lease incentives and initial direct costs incurred, as applicable.

As the implicit rate in the Company's leases is generally unknown, the Company uses its incremental borrowing rate based on the information available at the lease commencement date in determining the present value of future lease payments. When calculating the Company’s incremental borrowing rates, the Company gives consideration to its credit risk, term of the lease, total lease payments and adjust for the impacts of collateral, as necessary. The lease term used may reflect any option to extend or terminate the lease when it is reasonably certain the Company will exercise such options. Lease expenses for the Company's operating leases are recognized on a straight-line basis over the lease term.

ASU 2016-02 provides a number of optional practical expedients in transitioning to ASU 2016-02. The Company has elected the package of practical expedients to avoid reassessing under ASU 2016-02 prior conclusions about lease identification, lease classification and initial direct costs. The Company has also elected the practical expedient allowing the use of hindsight in determining the lease term and assessing impairment of right-of-use ROU assets based on all facts and circumstances through the effective date of the new standard. ASU 2016-02 also provides practical expedients for ongoing lease accounting. The Company has elected the recognition exemption for short-term leases for all leases that qualify. Under this exemption, the Company will not recognize ROU assets or lease liabilities for those leases that qualify as a short-term lease (leases with lease terms of 12 months or less), which includes not recognizing ROU assets or lease liabilities for existing short-term leases in transition. The Company also has elected the practical expedient avoid separating lease and non-lease components for any of its leases within its existing classes of assets.

8


The Company recognized operating lease liabilities of $78.8 and right-of-use assets related to operating leases totaling $74.5 as of the adoption date. These are presented as “Current maturities of operating lease liabilities” for a total of $13.1, “Noncurrent operating lease liabilities” for a total of $65.7, and “Operating lease right-of-use assets” for a total of $74.5 on the Company’s consolidated balance sheet. No adjustments to the beginning retained earnings balance were required.

period.

Recent Accounting Pronouncements
Recently Adopted Standards Effective in Future Years and Not Yet Adopted

In June 2016, the FASBFinancial Accounting Standards Board (the "FASB") issued ASU 2016-13, Financial Instruments – Credit Losses (Topic 326) (“ASU 2016-13”) which introduces new guidance for the accounting for credit losses on certain instruments within its scope. ASU 2016-13 introduces an approach based on expected losses to estimate credit losses on certain types of financial instruments. For trade receivables, the Company will beis required to use a forward-looking expected loss model rather than the incurred loss model for recognizing credit losses, which reflects losses that are probable. Credit losses relating to available-for-sale debt securities willare also be recorded through an allowance for credit losses rather than as a reduction in the amortized cost basis of the securities. On July 1, 2020, the Company adopted ASU 2016-13 under the modified retrospective approach by initially applying ASU 2016-13 at the adoption date, rather than at the beginning of the earliest comparative period presented. This guidance was adopted with no material impact to the Company's consolidated financial statements.
In August 2018, the FASB issued ASU 2018-15, Intangibles – Goodwill and Other - Internal-Use Software (Subtopic 350-40): Customer’s Accounting for Implementation Costs Incurred in a Cloud Computing Arrangement That Is a Service Contract (“ASU 2018-15”). ASU 2018-15 aligns the requirements for capitalizing implementation costs incurred in a hosting arrangement that is a service contract with the requirements for capitalizing implementation costs incurred to develop or obtain internal-use software, including hosting arrangements that include an internal-use
8

Table of Contents
software license. On July 1, 2020, the Company adopted ASU 2018-15 on a prospective basis with no material impact to the Company's consolidated financial statements as of September 30, 2020. The amounts capitalized may be material in future periods; implementation costs incurred in cloud computing arrangements are capitalized as part of the other assets financial statement line item in the consolidated balance sheets.
Standards Effective in Future Years and Not Yet Adopted
In December 2019, the FASB issued ASU 2019-12, Income Taxes (Topic 740): Simplifying the Accounting for Income Taxes ("ASU 2019-12"). ASC 2019-12 is a new accounting standard to simplify accounting for income taxes and remove, modify, and add to the disclosure requirements of income taxes. The standard is effective for fiscal years beginning after December 31, 2019, including interim periods within those years. Early application of the guidance is permitted for all entities for fiscal years beginning after December 15, 2018, including the interim periods within those fiscal years. Application of the amendments is through a cumulative-effect adjustment to retained earnings as of the effective date.2020, with early adoption permitted. The Company is currently evaluating the impact of ASU 2016-13this new standard will have on itsthe consolidated financial statementsstatements.
.(2)

REVENUE

(2)

REVENUE

Myriad generates revenue by performing molecular diagnostic testing and pharmaceutical services. The Company previously provided clinical services until selling Privatklinik Dr. Robert Schindlbeck GmbH & Co. KG (the "Clinic") in February 2020. Revenue from the sale of molecular diagnostic tests and pharmaceutical and clinical services is recorded at the estimated amount of consideration to be received. The Company has determined that the communication of test results or the completion of clinical and pharmaceutical services indicates transfer of control for revenue recognition purposes.

The following table presents detail regarding the composition of our total revenue by product and U.Sby U.S. versus rest of world, “RoW”:

 

Three months ended September 30,

 

Three months ended September 30,

 

2019

 

 

2018

 

20202019

(In millions)

 

U.S.

 

 

RoW

 

 

Total

 

 

U.S.

 

 

RoW

 

 

Total

 

(In millions)U.S.RoWTotalU.S.RoWTotal

Molecular diagnostic revenues:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Molecular diagnostic revenues:

Hereditary Cancer Testing

 

$

100.6

 

 

$

3.9

 

 

$

104.5

 

 

$

113.5

 

 

$

2.8

 

 

$

116.3

 

Hereditary Cancer Testing$72.1 $8.5 $80.6 $100.6 $3.9 $104.5 
PrenatalPrenatal16.4 0.1 16.5 23.5 23.5 

GeneSight

 

 

22.7

 

 

 

 

 

 

22.7

 

 

 

29.3

 

 

 

 

 

 

29.3

 

GeneSight11.911.922.722.7

Prenatal

 

 

23.5

 

 

 

 

 

 

23.5

 

 

 

18.1

 

 

 

 

 

 

18.1

 

VectraDA

 

 

11.0

 

 

 

 

 

 

11.0

 

 

 

13.0

 

 

 

 

 

 

13.0

 

VectraVectra9.19.111.011.0
myChoice CDxmyChoice CDx7.60.2 7.81.31.3

Prolaris

 

 

6.5

 

 

 

 

 

 

6.5

 

 

 

6.2

 

 

 

 

 

 

6.2

 

Prolaris6.46.46.56.5

EndoPredict

 

 

0.5

 

 

 

1.8

 

 

 

2.3

 

 

 

0.3

 

 

 

2.1

 

 

 

2.4

 

EndoPredict0.42.42.80.51.82.3

Other

 

 

1.4

 

 

 

0.1

 

 

 

1.5

 

 

 

3.6

 

 

 

0.1

 

 

 

3.7

 

Other0.60.60.10.10.2

Total molecular diagnostic revenue

 

 

166.2

 

 

 

5.8

 

 

 

172.0

 

 

 

184.0

 

 

 

5.0

 

 

 

189.0

 

Total molecular diagnostic revenue124.511.2135.7166.25.8172.0

Pharmaceutical and clinical service revenue

 

 

8.5

 

 

 

5.9

 

 

 

14.3

 

 

 

7.6

 

 

 

5.7

 

 

 

13.3

 

Pharmaceutical and clinical service revenue9.59.58.55.914.3

Total revenue

 

$

174.7

 

 

$

11.7

 

 

$

186.3

 

 

$

191.6

 

 

$

10.7

 

 

$

202.3

 

Total revenue$134.0 $11.2 $145.2 $174.7 $11.7 $186.3 


The Company performs its obligation under a contract with a customer by processing diagnostic tests and communicating the test results to customers, in exchange for consideration from the customer. The Company has the right to bill its customers upon the completion of performance obligations and thus does not record contract assets. Occasionally, customers make payments prior to the Company's performance of its contractual obligations. When this occurs, the Company records a contract liability as deferred revenue. During fiscal year 2020, the Company received approximately $29.7 in advance Medicare payments to provide relief from the economic impacts of COVID-19 on the Company. The advance Medicare payments are included in the beginning and ending balance of deferred revenue. A reconciliation of the beginning and ending balances of deferred revenue is shown in the table below:

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Deferred revenue - beginning balance

 

$

2.2

 

 

$

2.6

 

Revenue recognized

 

 

(0.4

)

 

 

(1.7

)

Prepayments

 

 

0.3

 

 

 

1.6

 

Deferred revenue - Ending Balance

 

$

2.1

 

 

$

2.5

 

9

9


Myriad Companies generate revenue by performing molecular diagnostic testing and pharmaceutical & clinical services. Revenue from the saleTable of molecular diagnostic tests and pharmaceutical and clinical services is recorded at the invoiced amount net of any discounts or contractual allowances. The Company has determined that the communication of test results or the completion of clinical and pharmaceutical services indicates transfer of control for revenue recognition purposes.Contents

Three months ended
September 30,
20202019
Deferred revenue - beginning balance$32.8 $2.2 
Revenue recognized(2.3)(0.4)
Prepayments1.8 0.3 
Deferred revenue - ending balance$32.3 $2.1 
In accordance with ASU 2014-09, the Company has elected not to disclose the aggregate amount of the transaction price allocated to remaining performance obligations for its contracts that are one year or less, as the revenue is expected to be recognized within the next year. Furthermore, the Company has elected not to disclose the aggregate amount of the transaction price allocated to remaining performance obligations for its agreements wherein the Company’s right to payment is in an amount that directly corresponds with the value of Company’s performance to date. However, periodically the Company periodically enters into arrangements with customers to provide diagnostic testing and/or pharmaceutical and clinical services that may have terms longer than one year and include multiple performance obligations. As of September 30, 2019,2020, the aggregate amount of the transaction price of such contracts that is allocated to the remaining performance obligations is $1.8.  

$2.8. 

The Company provides discounts such as early payment, self-pay and volumemay provide discounts to its customers. In determining the transaction price, Myriad includes an estimate of the expected amount of consideration as revenue. The Company applies this method consistently for similar contracts when estimating the effect of any uncertainty on an amount of variable consideration to which it will be entitled. The Company applies the expected value method for sales where the Company has a large number of contracts with similar characteristics.


In addition, the Company considers all the information (historical, current, and forecast) that is reasonably available to identify possible consideration amounts. The Company considers the probability of the variable consideration for each possible scenario. The Company also has significant experience with historical discount patterns and uses this experience to estimate transaction prices. The Company excludes from the measurement of transaction price all taxes assessed by a governmental authority that are both imposed on and concurrent with a specific revenue-producing transaction and collected by the Company from a customercustomer. for e.g.example, sales tax, value added tax, etc.

When assessing the total consideration for insurance carriers and patients, revenues are further constrained for estimated refunds. The Company reserves certain amounts in accrued liabilities on the balance sheet in anticipation of requests for refunds of payments made previously by insurance carriers, which are accounted for as reductions in revenues in the consolidated statements of operations and comprehensive loss. As of September 30, 2020, the Company recorded a $2.2 accrued liability and corresponding reduction in revenues for future refund of payments.


Cash collections for certain diagnostic tests delivered may differ from rates originally estimated, primarily driven by changes in the estimated transaction price due to contractual adjustments, obtaining updated information from payors and patients that was unknown at the time the performance obligation was met and settlements with third party payors. As a result of this new information, the Company updates our estimate of the amounts to be recognized for previously delivered tests, the impact of which was not material to our consolidated statements of operations for the three months ended September 30, 2020.
The Company applies the practical expedient related to costs to obtain or fulfill a contract since the amortization period for such costs will be one year or less. Accordingly, 0 costs incurred to obtain or fulfill a contract have been capitalized. The Company also applies the practical expedient for not adjusting revenue recognized for the effects of the time value of money. This practical expedient has been elected because the Company collects very little cash from customers under payment terms and the vast majority of paymentspayment terms have a payback period of less than one year.

During

Concentration of Credit Risk
Financial instruments that potentially subject us to concentrations of credit risk consist primarily of cash and cash equivalents and accounts receivable. Substantially all of the Company’s accounts receivable are with companies in the healthcare industry, U.S. and state governmental agencies that make payments on the customer's behalf, and with individuals. The Company does not believe that receivables due from U.S. and state governmental agencies, such as Medicare, represent a credit risk since the related healthcare programs are funded by the U.S. and state governments. The Company only has one payor, Medicare, that represents greater than 10% of its revenues. Revenues received from Medicare represented approximately 16% and 14% of total revenue for the three months ended September 30, 2020 and 2019, the Company recognized a $10.9 decrease in revenue, which resulted in an ($0.11) impact to EPS, for tests in which the performance obligationrespectively. Concentrations of delivering the tests results was met in prior periods.  The changes were primarily driven by changes in the estimated transaction pricecredit risk are mitigated due to contractual adjustments, obtaining updated information from payors and patients that was unknown at the time the performance obligation was met and settlements with third party payors.

(3)

ACQUISITIONS

Acquisition of Counsyl, Inc.

On July 31, 2018, the Company completed the acquisition of Counsyl, Inc. (“Counsyl”), a leading provider of genetic testing and DNA analysis services, pursuant to the Agreement and Plan of Merger (the “Merger Agreement”), dated May 25, 2018.  Pursuant to the termsnumber of the Merger Agreement, Myriad Merger Sub, Inc., a newly-created wholly-owned subsidiaryCompany’s customers as well as their dispersion across many geographic regions. No payor accounted for more than 10% of the Company, was merged with and into Counsyl, with Counsyl continuing as the surviving corporation and a wholly-owned subsidiary of Myriad.accounts receivable at September 30, 2020 or 2019. The Company believes the acquisition allows for greater entry into the high-growth reproductive testing market, with the ability to become a leader in women’s health genetic testing.  

The Company acquired Counsyl for total considerationdoes not require collateral from its customers.

10

Table of $405.9, consisting of $278.5 in cash, financed in part by the Amendment to the Facility (see Note 8) and 2,994,251 shares of common stock issued, valued at $127.4.  The shares were issued and valued as of July 31, 2018 at a per share market closing price of $42.53. To complete the purchase transaction, the Company incurred approximately $6.8 of acquisition costs, which were recorded as selling, general and administrative expenses in the period incurred.

Of the cash consideration, $5.0 was deposited into an escrow account to fund any post-closing adjustments payable to Myriad based upon differences between the estimated working capital and the actual working capital of Counsyl at closing.

10


Contents

Consideration transferred was allocated to the tangible and intangible assets acquired and liabilities assumed based on their fair values as of the acquisition date. Management estimated the fair value of tangible and intangible assets and liabilities in accordance with the applicable accounting guidance for business combinations and utilized the services of third-party valuation consultants. The allocation of the consideration transferred was finalized within the measurement period (which was up to one year from the acquisition date).

 

 

Estimated Fair

Value

 

Current assets

 

$

42.5

 

Intangible assets

 

 

290.0

 

Equipment

 

 

18.2

 

Other assets

 

 

0.1

 

Goodwill

 

 

99.3

 

Current liabilities

 

 

(19.6

)

Long term liabilities

 

 

(0.1

)

Deferred tax liability

 

 

(9.2

)

Total fair value purchase price

 

$

421.2

 

Less: Cash acquired

 

 

(15.3

)

Total consideration transferred

 

$

405.9

 

Identifiable Intangible Assets

Through its acquisition of Counsyl, the Company acquired intangible assets that consisted of developed screening processes with an estimated fair value of $290.0. The fair values of these developed screening processes were estimated using a probability-weighted income approach that discounts expected future cash flows to present value. Under the probability-weighted income approach, the estimated net cash flows from these developed screening processes were discounted using a discount rate of 12.5%, which is based on the estimated internal rate of return for the acquired developed screening processes and represents the rate that market participants may use to value these intangible assets. The Company will amortize these intangible assets on a straight-line basis over their estimated useful lives of 12 years.      

Goodwill

The goodwill represents the excess of consideration transferred over the fair value of assets acquired and liabilities assumed from Counsyl and is attributable to the benefits expected from combining the Company’s expertise with Counsyl’s technology and customer insights and the opportunity to integrate genetic screening into clinical practice with OBGYNs.  Changes in goodwill since the Counsyl acquisition as of September 30, 2019 are shown below:

 

 

Carrying

 

 

 

amount

 

Balance September 30, 2018

 

$

94.9

 

Fair value adjustment to equipment

 

 

0.7

 

Intangible adjustment

 

 

2.9

 

Working capital adjustment

 

 

(1.1

)

Change in deferred tax liability

 

 

1.9

 

Balance September 30, 2019

 

$

99.3

 

(3)MARKETABLE INVESTMENT SECURITIES

This goodwill is not deductible for income tax purposes.

Pro Forma Information (Unaudited)

The unaudited pro-forma results presented below include the effects of the Counsyl acquisition as if it had been consummated as of July 1, 2017, with adjustments to give effect to pro forma events that are directly attributable to the acquisition, which includes adjustments related to the amortization of acquired intangible assets, interest income and expense, and depreciation.

11


The unaudited pro forma results do not reflect any operating efficiency or potential cost savings that may result from the consolidation of Counsyl. Accordingly, these unaudited pro forma results are presented for informational purposes only and are not necessarily indicative of what the actual results of operation of the combined company would have been if the acquisition had occurred at the beginning of the period presented, nor are they indicative of future results of operations and are not necessarily indicative of results that might have been achieved had the acquisition been consummated as of July 1, 2017.

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Revenue

 

$

186.3

 

 

$

212.5

 

Income (loss) from operations

 

 

(20.9

)

 

 

11.5

 

Net income (loss)

 

 

(20.6

)

 

 

8.6

 

Earnings (loss) per share, basic

 

$

(0.28

)

 

$

0.11

 

Earnings (loss) per share, diluted

 

$

(0.28

)

 

$

0.11

 

(4)

MARKETABLE INVESTMENT SECURITIES

The Company has classified its marketabledebt investment securities as available-for-sale securities. These securities are carried at estimated fair value with unrealized holding gains and losses, net of the related tax effect, included in accumulated other comprehensive loss in stockholders’ equity until realized. Gains and losses on investment security transactions are reported on the specific-identification method. Dividend and interest income are recognized when earned. The Company’s cash equivalents consist of short-term, highly liquid investments that are readily convertible to known amounts of cash. The amortized cost, gross unrealized holding gains, gross unrealized holding losses, and fair value for available-for-sale securities by major security type and class of security at September 30, 20192020 and June 30, 20192020 were as follows:

 

 

 

 

 

Gross

 

 

Gross

 

 

 

 

 

 

 

 

 

 

unrealized

 

 

unrealized

 

 

 

 

 

Amortized
cost
Gross
unrealized
holding
gains
Gross
unrealized
holding
losses
Estimated
fair value

 

Amortized

 

 

holding

 

 

holding

 

 

Estimated

 

 

cost

 

 

gains

 

 

losses

 

 

fair value

 

At September 30, 2019:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

At September 30, 2020:At September 30, 2020:

Cash and cash equivalents:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Cash and cash equivalents:

Cash

 

$

67.2

 

 

$

 

 

$

 

 

$

67.2

 

Cash$68.3 $— $— $68.3 

Cash equivalents

 

 

22.7

 

 

 

 

 

 

 

 

$

22.7

 

Cash equivalents50.0 — — $50.0 

Total cash and cash equivalents

 

 

89.9

 

 

 

 

 

 

 

 

 

89.9

 

Total cash and cash equivalents118.3 — — 118.3 

Available-for-sale:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Available-for-sale:

Corporate bonds and notes

 

 

68.7

 

 

 

0.4

 

 

 

 

 

 

 

69.1

 

Corporate bonds and notes40.5 0.6 41.1 

Municipal bonds

 

 

15.0

 

 

 

0.1

 

 

 

 

 

 

 

15.1

 

Municipal bonds12.6 0.2 12.8 

Federal agency issues

 

 

7.0

 

 

 

 

 

 

 

 

 

7.0

 

Federal agency issues4.0 0.1 4.1 

US government securities

 

 

12.9

 

 

 

0.1

 

 

 

 

 

 

13.0

 

US government securities14.2 0.1 14.3 

Total

 

$

193.5

 

 

$

0.6

 

 

$

 

 

$

194.1

 

Total$189.6 $1.0 $$190.6 

 

 

 

 

 

Gross

 

 

Gross

 

 

 

 

 

 

 

 

 

 

unrealized

 

 

unrealized

 

 

 

 

 

Amortized
cost
Gross
unrealized
holding
gains
Gross
unrealized
holding
losses
Estimated
fair value

 

Amortized

 

 

holding

 

 

holding

 

 

Estimated

 

 

cost

 

 

gains

 

 

losses

 

 

fair value

 

At June 30, 2019:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

At June 30, 2020:At June 30, 2020:

Cash and cash equivalents:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Cash and cash equivalents:

Cash

 

$

68.7

 

 

$

 

 

$

 

 

$

68.7

 

Cash$132.8 $— $— $132.8 

Cash equivalents

 

 

24.5

 

 

 

 

 

 

 

 

 

24.5

 

Cash equivalents30.9 — — 30.9 

Total cash and cash equivalents

 

 

93.2

 

 

 

 

 

 

 

 

 

93.2

 

Total cash and cash equivalents163.7 — — 163.7 

Available-for-sale:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Available-for-sale:

Corporate bonds and notes

 

 

64.0

 

 

 

0.6

 

 

 

 

 

 

64.6

 

Corporate bonds and notes50.1 0.8 50.9 

Municipal bonds

 

 

15.3

 

 

 

 

 

 

 

 

 

15.3

 

Municipal bonds17.8 0.2 18.0 

Federal agency issues

 

 

9.0

 

 

 

 

 

 

 

 

 

9.0

 

Federal agency issues5.5 0.1 5.6 

US government securities

 

 

9.7

 

 

 

 

 

 

 

 

 

9.7

 

US government securities16.4 0.2 16.6 

Total

 

$

191.2

 

 

$

0.6

 

 

$

 

 

$

191.8

 

Total$253.5 $1.3 $$254.8 

12

In accordance with the adoption of ASC 2016-13, the Company assesses any unrealized loss positions for available-for-sale debt securities for which an allowance for credit losses has not been recorded. The aggregate amount of unrealized losses of these securities was not significant, and the impact of the securities in a continuous loss position to the condensed consolidated statements of operations and comprehensive loss were not material as of September 30, 2020.

11

Table of Contents
Cash, cash equivalents, and maturities of debt securities classified as available-for-sale securities are as follows at September 30, 2019:

2020:

 

Amortized

 

 

Estimated

 

 

cost

 

 

fair value

 

Amortized
cost
Estimated
fair value

Cash

 

$

67.2

 

 

$

67.2

 

Cash$68.3 $68.3 

Cash equivalents

 

 

22.7

 

 

 

22.7

 

Cash equivalents50.0 50.0 

Available-for-sale:

 

 

 

 

 

 

 

 

Available-for-sale:

Due within one year

 

 

54.9

 

 

 

55.0

 

Due within one year41.8 42.1 

Due after one year through five years

 

 

48.7

 

 

 

49.2

 

Due after one year through five years29.5 30.2 

Due after five years

 

 

 

 

 

 

Due after five years

Total

 

$

193.5

 

 

$

194.1

 

Total$189.6 $190.6 

(5)

PROPERTY, PLANT AND EQUIPMENT, NET

 

 

September 30,

 

 

June 30,

 

 

 

2019

 

 

2019

 

Land

 

$

2.2

 

 

$

2.3

 

Buildings and improvements

 

 

18.2

 

 

 

18.8

 

Leasehold improvements

 

 

31.1

 

 

 

31.0

 

Equipment

 

 

115.5

 

 

 

117.1

 

 

 

 

167.0

 

 

 

169.2

 

Less accumulated depreciation

 

 

(112.0

)

 

 

(111.9

)

Property, plant and equipment, net

 

$

55.0

 

 

$

57.3

 

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Depreciation expense

 

$

2.9

 

 

$

4.9

 

(4)FAIR VALUE MEASUREMENTS

(6)

GOODWILL AND INTANGIBLE ASSETS

Goodwill

The fair value of the Company’s financial instruments reflects the amounts that the Company has recorded goodwillestimates it will receive in connection with the sale of $416.1 froman asset or pay in connection with the acquisitionstransfer of Counsyla liability in an orderly transaction between market participants at the measurement date (exit price). The fair value hierarchy prioritizes the use of inputs used in valuation techniques into the following three levels:

Level 1—quoted prices in active markets for identical assets and liabilities.
Level 2—observable inputs other than quoted prices in active markets for identical assets and liabilities; quoted prices in markets that was completedare not active; or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities.  Some of the Company’s marketable securities primarily utilize broker quotes in a non-active market for valuation of these securities.
Level 3—unobservable inputs.
All of the Company’s financial instruments are valued using quoted prices in active markets or based on July 31, 2018, Assurexother observable inputs.  For Level 2 securities, the Company uses a third party pricing service which provides documentation on an ongoing basis that was completed on August 31, 2016,includes, among other things, pricing information with respect to reference data, methodology, inputs summarized by asset class, pricing application and corroborative information. The fair value of contingent consideration related to the Sividon Diagnostics GmbH (“Sividon”("Sividon") acquisition in fiscal year 2016 as well as long-term debt are categorized as Level 3 liabilities, as the measurement amount is based primarily on significant inputs not observable in the market.  For Level 3 contingent consideration, the Company reassesses the fair value of expected contingent consideration and the corresponding liability each reporting period using the Monte Carlo Method, which is consistent with the initial measurement of the expected earn out liability. This fair value measurement is considered a Level 3 measurement because the Company estimates projections during the expected measurement period of approximately 9.25 years, utilizing various potential pay-out scenarios.  Probabilities were applied to each potential scenario and the resulting values were discounted using a rate that was completed on May 31, 2016, Privatklinik Dr. Robert Schindlbeck GmbH & Co. KG (the “Clinic”) that was completed on February 27, 2015, Crescendo Bioscience, Inc. that was completed on February 28, 2014considers weighted average cost of capital as well as a specific risk premium associated with the riskiness of the earn-out itself, the related projections, and Rules-Based Medicine, Inc. that was completed on May 31, 2011.  Of this goodwill, $350.8 relatesthe overall business. The contingent earn-out liabilities are classified as a component of long-term and short-term contingent consideration in the Company’s consolidated balance sheets.  Changes to the Company’s diagnostic segment and $65.3 relatesearn-out liabilities are reflected in change in the fair value of contingent consideration in our consolidated statements of operations. Changes to the other segment.  unobservable inputs could have a material impact on the Company’s financial statements.
The fair value of our long-term debt, which we consider a Level 3 measurement, is estimated using discounted cash flow analyses, based on the Company’s current estimated incremental borrowing rates for similar borrowing arrangements.  The fair value of long-term debt is estimated to be $226.5 at September 30, 2020.

12

Table of Contents
The following summarizes changes totable sets forth the goodwillfair value of the financial assets and liabilities that the Company re-measures on a regular basis:
Level 1Level 2Level 3Total
September 30, 2020
Money market funds (a)$50.0 $$$50.0 
Corporate bonds and notes41.1 41.1 
Municipal bonds12.8 12.8 
Federal agency issues4.1 4.1 
US government securities14.3 14.3 
Contingent consideration(5.9)(5.9)
Total$50.0 $72.3 $(5.9)$116.4 
(a)Money market funds are primarily comprised of exchange traded funds and accrued interest.
Level 1Level 2Level 3Total
June 30, 2020
Money market funds (a)$30.9 $$$30.9 
Corporate bonds and notes50.9 50.9 
Municipal bonds18.0 18.0 
Federal agency issues5.6 5.6 
US government securities16.6 16.6 
Contingent consideration(6.8)(6.8)
Total$30.9 $91.1 $(6.8)$115.2 
(a)Money market funds are primarily comprised of exchange traded funds and accrued interest.

The following table reconciles the change in the fair value of the contingent consideration during the periods presented:
Carrying
amount
Balance June 30, 2020$6.8 
Payment of contingent consideration(0.1)
Change in fair value recognized in the income statement(1.1)
Translation adjustments recognized in other comprehensive loss0.3 
Ending balance September 30, 2020$5.9 

The fair value of contingent consideration for the three months ended September 30, 2019:

2020 decreased compared to the same period in the prior year due to changes in timing of expected cash payments associated with the contingent consideration related to the Sividon acquisition.  

 

 

Carrying

amount

 

Ending balance June 30 2019

 

$

417.2

 

Acquisitions

 

 

 

Translation adjustments

 

 

(1.1

)

Ending balance September 30, 2019

 

$

416.1

 

(5)PROPERTY, PLANT AND EQUIPMENT, NET
September 30,
2020
June 30,
2020
Leasehold improvements$32.6 $31.8 
Equipment114.1 112.1 
146.7 143.9 
Less accumulated depreciation(110.0)(106.9)
Property, plant and equipment, net$36.7 $37.0 

13


Table of Contents
Three months ended
September 30,
20202019
Depreciation expense$2.4 $2.9 

(6)GOODWILL AND INTANGIBLE ASSETS
Goodwill
The changes in the carrying amount of goodwill for the three months ended September 30, 2020, are as follows:
DiagnosticOtherTotal
Beginning balance$270.7 $56.9 $327.6 
Translation adjustments0.7 0.7 
Ending balance$271.4 $56.9 $328.3 

The Company will perform its annual goodwill impairment testing during the quarter ended December 31, 2020 as a result of its change in fiscal year end (see Note 16). The upcoming annual assessment may result in impairment charges if there is deterioration in business conditions, negative changes in market factors, or changes in the strategic priorities of the Company and its reporting units.
Intangible Assets

Intangible assets primarily consist of amortizable assets of purchased licenses and technologies, customer relationships, and trade names as well as non-amortizable intangible assets of in-process technologies and research and development. The following summarizes the amounts reported as intangible assets:

 

Gross

 

 

 

 

 

 

 

 

 

 

Carrying

 

 

Accumulated

 

 

 

 

 

Gross
Carrying
Amount
Accumulated
Amortization
Net

 

Amount

 

 

Amortization

 

 

Net

 

At September 30, 2019:

 

 

 

 

 

 

 

 

 

 

 

 

At September 30, 2020:At September 30, 2020:

Purchased licenses and technologies

 

$

814.5

 

 

$

(171.5

)

 

$

643.0

 

Purchased licenses and technologies$816.6 $(232.4)$584.2 

Customer relationships

 

 

4.7

 

 

 

(3.9

)

 

 

0.8

 

Customer relationships4.7 (4.4)0.3 

Trademarks

 

 

3.0

 

 

 

(1.3

)

 

 

1.7

 

Trademarks3.0 (1.4)1.6 

Total amortized intangible assets

 

 

822.2

 

 

 

(176.7

)

 

 

645.5

 

Total amortized intangible assets824.3 (238.2)586.1 

In-process research and development

 

 

22.3

 

 

 

 

 

 

22.3

 

In-process research and development4.8 — 4.8 

Total unamortized intangible assets

 

 

22.3

 

 

 

 

 

 

22.3

 

Total unamortized intangible assets4.8 — 4.8 

Total intangible assets

 

$

844.5

 

 

$

(176.7

)

 

$

667.8

 

Total intangible assets$829.1 $(238.2)$590.9 

 

Gross

 

 

 

 

 

 

 

 

 

 

Carrying

 

 

Accumulated

 

 

 

 

 

Gross
Carrying
Amount
Accumulated
Amortization
Net

 

Amount

 

 

Amortization

 

 

Net

 

At June 30, 2019:

 

 

 

 

 

 

 

 

 

 

 

 

At June 30, 2020:At June 30, 2020:

Purchased licenses and technologies

 

$

815.7

 

 

$

(156.6

)

 

$

659.1

 

Purchased licenses and technologies$815.6 $(217.1)$598.5 

Customer relationships

 

 

4.6

 

 

 

(3.8

)

 

 

0.8

 

Customer relationships4.6 (4.2)0.4 

Trademarks

 

 

3.0

 

 

 

(1.2

)

 

 

1.8

 

Trademarks3.0 (1.4)1.6 

Total amortized intangible assets

 

 

823.3

 

 

 

(161.6

)

 

 

661.7

 

Total amortized intangible assets823.2 (222.7)600.5 

In-process research and development

 

 

23.0

 

 

 

 

 

 

23.0

 

In-process research and development4.8 — 4.8 

Total unamortized intangible assets

 

 

23.0

 

 

 

 

 

 

23.0

 

Total unamortized intangible assets4.8 — 4.8 

Total intangible assets

 

$

846.3

 

 

$

(161.6

)

 

$

684.7

 

Total intangible assets$828.0 $(222.7)$605.3 


14

Table of Contents
The Company recorded amortization expense during the respective periods for these intangible assets as follows:

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Amortization of intangible assets

 

$

15.3

 

 

$

13.4

 

Three months ended
September 30,
20202019
Amortization of intangible assets$15.3 $15.3 

(7)

ACCRUED LIABILITIES

 

 

September 30,

 

 

June 30,

 

 

 

2019

 

 

2019

 

Employee compensation and benefits

 

$

45.2

 

 

$

48.8

 

Accrued taxes payable

 

 

7.2

 

 

 

3.0

 

Qui tam settlement

 

 

9.1

 

 

 

9.1

 

Other

 

 

11.5

 

 

 

18.0

 

Total accrued liabilities

 

$

73.0

 

 

$

78.9

 

(7)ACCRUED LIABILITIES

(8)

LONG-TERM DEBT

September 30,
2020
June 30,
2020
Employee compensation and benefits$47.2 $47.4 
Accrued taxes payable3.5 6.1 
Other14.7 22.4 
Total accrued liabilities$65.4 $75.9 

(8)LONG-TERM DEBT
On December 23, 2016, the Company entered into a senior secured revolving credit facility (the “Facility”) by and among Myriad, as borrower, withand the lenders from time to time party thereto. On July 31, 2018, the Company entered into Amendment No. 1 (the “Amended Facility”) which effectseffected an “amend and extend” transaction with respect to the Facility by which the maturity date thereof was extended to July 31, 2023 and the maximum aggregate principal commitment was increased from $300.0 to $350.0. This wasOn May 1, 2020, the Company entered into Amendment No. 2 (the “Amended Facility”), which waived the Company's compliance with certain covenants and modified the interest rate and other terms during the Amendment Period from March 31, 2020 through June 30, 2021 (the "Amendment Period"). Both amendments were accounted for as a modificationmodifications pursuant to guidance in ASC 470-50.

Pursuant to the Amended Facility, Myriadthe Company borrowed revolving loans in an aggregate principal amount of $300.0 with $1.8 in upfront fees and $0.3 debt issuance costs recorded as a debt discount to be amortized over the term of the Amended Facility. The Company incurred an additional $1.0 in upfront fees as a result of Amendment No. 2, which was also recorded as a debt discount that will be amortized over the term of the Amended Facility. The current balance of the net long-term debt is $225.0.$224.6. There are 0 scheduled principal payments of the Amended Facility prior to its maturity date.

14


The proceeds of the Amended Facility were used to: (i) refinance in full the obligations under the Facility, (ii) finance the acquisition of Counsyl (See Note 3), (iii) pay fees, commissions, transactions costs and expenses incurred in connection with the foregoing, and (iv) for working capital and other general corporate purposes.

The Amended Facility contains customary loan terms, interest rates, representations and warranties, affirmative and negative covenants, in each case, subject to customary limitations, exceptions and exclusions. The Amended Facility also contains certain customary events of default.

Amendment No. 2 modified the Facility to increase the interest rate to be fixed at a spread of LIBOR plus 350 basis points on drawn balance and the undrawn fee was increased to 50 basis points during the Amendment Period. At the end of the Amendment Period, interest rates return to the previous pricing of 200 basis points on drawn balances and an undrawn fee ranging from 25 to 45 basis points based on the Company's leverage ratio. The LIBOR floor was also increased to 1.0% during the Amendment Period. The interest rate as of September 30, 2020 was 4.5%.

Covenants in the Amended Facility impose operating and financial restrictions on the Company. These restrictions may prohibit or place limitations on, among other things, the Company’s ability to incur additional indebtedness, create certain types of liens, and complete mergers, consolidations, or consolidations, and/orcomplete change in control transactions. The Amended Facility may also prohibit or place limitations on the Company’s ability to sell assets, pay dividends or provide other distributions to shareholders. The Company must maintain specified leverage and interest ratios measured as of the end of each quarter as a financial covenant in the Amended Facility. WeAmendment No. 2 modified the Amended Facility's compliance with the leverage covenant and the interest coverage ratio covenant, which were waived through March 31, 2021. A minimum liquidity covenant was added for the period beginning May 2020 until March 2021, and a minimum EBITDA covenant was added for the quarters ending December 31, 2020 and March 31, 2021. Amendment No. 2 also revised certain negative covenants of the Amended Facility during the Amendment Period. The Company was in compliance with all financial covenants at September 30, 2019.

During2020. Based on the quarter ended September 30, 2019,continued uncertainty regarding the impact of COVID-19 on the Company’s future operations, it is possible that the Company made $8.6could be in principal repayments.

violation of certain financial covenants contained in the Amended Facility within the Amendment Period, which runs through June 30, 2021. The Company may seek waivers or amendments from the lenders in order to avoid a future potential covenant violation, in addition to taking other potential actions. If the Company were unable to comply with the covenants in the future, it could result in an increase in the rate of interest and limits on the Company's ability to incur certain additional indebtedness and it could potentially cause the loan repayment to be

15

Table of Contents
accelerated, any of which could have a material adverse impact on the Company’s operations and liquidity. The Company has and continues to take actions to mitigate the risk of an event of default under the Amended Facility, however there is no assurance it will be successful in doing so.
The Amended Facility is secured by a first-lien security interest in substantially all of the assets of Myriad and certain of its domestic subsidiaries and each such domestic subsidiary of Myriad has guaranteed the repayment of the Amended Facility. Amounts outstanding under the Amended Facility and Facility were as follows:

 

September 30,

 

 

June 30,

 

 

2019

 

 

2019

 

September 30,
2020
June 30,
2020

Long-term debt

 

$

226.6

 

 

$

235.0

 

Long-term debt$226.7 $226.7 

Long-term debt discount

 

 

(1.6

)

 

 

(1.5

)

Long-term debt discount(2.1)(2.3)

Net long-term debt

 

$

225.0

 

 

$

233.5

 

Net long-term debt$224.6 $224.4 

(9)

OTHER LONG TERM LIABILITIES

 

 

September 30,

 

 

June 30,

 

 

 

2019

 

 

2019

 

Pension obligation

 

 

6.8

 

 

 

6.8

 

Other

 

 

0.5

 

 

 

1.0

 

Total other long term liabilities

 

$

7.3

 

 

$

7.8

 

(9)OTHER LONG-TERM LIABILITIES
September 30,
2020
June 30,
2020
Contingent consideration$2.6 $3.7 
Other8.1 4.3 
Total other long-term liabilities$10.7 $8.0 

The Company has 2 non-contributory defined benefit pension plans for certain Clinic employees. Participation in the plans excludes those employees hired after 2002. AsCompany's balance of other long-term liabilities as of September 30, 2019 the fair value2020 and June 30, 2020 consists of the plan assets were approximately $0.1 resulting in a net pension liabilityCompany's portion of $6.8.social security taxes that have been deferred under the CARES Act that do not have to be deposited until December 2021 and December 2022.
(10)

PREFERRED AND COMMON STOCKHOLDERS' EQUITY

(10)

PREFERRED AND COMMON STOCKHOLDER’S EQUITY

The Company is authorized to issue up to 5.0 shares of preferred stock, par value $0.01 per share.  There were 0 preferred shares outstanding at September 30, 2019.

2020.

The Company is authorized to issue up to 150.0 shares of common stock, par value $0.01 per share. There were 74.475.2 shares issued and outstanding at September 30, 2019.

2020.

Common shares issued and outstanding

 

Three months ended

 

 

Year ended

 

 

September 30,

 

 

June 30,

 

Three months ended
September 30,
Year ended June 30,

 

2019

 

 

2019

 

20202020

Beginning common stock issued and outstanding

 

 

73.5

 

 

 

70.6

 

Beginning common stock issued and outstanding74.7 73.5 

Common stock issued upon exercise of options and employee

stock plans

 

 

0.9

 

 

 

4.5

 

Repurchase and retirement of common stock

 

 

 

 

 

(1.6

)

Common stock issued upon exercise of options, vesting of restricted stock units and employee stock plansCommon stock issued upon exercise of options, vesting of restricted stock units and employee stock plans0.5 1.2 

Common stock issued and outstanding at end of period

 

 

74.4

 

 

 

73.5

 

Common stock issued and outstanding at end of period75.2 74.7 

15


Basic earnings per share is computed based on the weighted-average number of shares of common stock outstanding.  Diluted earnings per share is computed based on the weighted-average number of shares of common stock, including the dilutive effect of common stock equivalents, outstanding.  In periods when the Company has a net loss, stock awards are excluded from the calculation of diluted net loss per share as their inclusion would have an antidilutive effect.
16

Table of Contents

The following is a reconciliation of the denominators of the basic and diluted earnings per share (“EPS”) computations:

 

Three months ended

 

 

September 30,

 

Three months ended
September 30,

 

2019

 

 

2018

 

20202019

Denominator:

 

 

 

 

 

 

 

 

Denominator:

Weighted-average shares outstanding used to compute

basic EPS

 

 

73.7

 

 

 

73.0

 

Weighted-average shares outstanding used to compute basic EPS74.7 73.7 

Effect of dilutive shares

 

 

 

 

 

 

Effect of dilutive shares

Weighted-average shares outstanding and dilutive

securities used to compute diluted EPS

 

 

73.7

 

 

 

73.0

 

Weighted-average shares outstanding and dilutive securities used to compute diluted EPS74.7 73.7 

Certain outstanding options and restricted stock units (“RSUs”) were excluded from the computation of diluted earnings per share because the effect would have been anti-dilutive. These potential dilutive common shares, which may be dilutive to future diluted earnings per share, are as follows:

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Anti-dilutive options and RSU's excluded from EPS

   computation

 

 

1.7

 

 

 

4.1

 

Three months ended
September 30,
20202019
Anti-dilutive options and RSUs excluded from EPS computation7.3 1.7 

Stock Repurchase Program

In June 2016, the Company’s Board of Directors authorized an eightha share repurchase program of $200.0 of the Company’s outstanding common stock. The Company plans to repurchase its common stock from time to time or on an accelerated basis through open market transactions or privately negotiated transactions as determined by the Company’sCompany's management. The amount and timing of stock repurchases under the program will depend on business and market conditions, stock price, trading restrictions, acquisition activity and other factors.  As of September 30, 2019,2020, the Company hasis authorized to repurchase up to $110.7 remaining on its current share repurchaseof shares under this authorization.

The Company uses NaN shares were repurchased during the par value method of accounting for its stock repurchases.  As a result of the stock repurchases, the Company reduced common stock and additional paid-in capital and recorded charges to accumulated deficit.  The shares retired, aggregate common stock and additional paid-in capital reductions, and related charges to accumulated deficit for the repurchases for three months ended September 30, 2020 or 2019.

(11)SHARE-BASED COMPENSATION
On November 30, 2017, the Company’s shareholders approved the adoption of the 2017 Employee, Director and Consultant Equity Incentive Plan (as amended, the “2017 Plan”). On November 29, 2018 and December 5, 2019, the shareholders approved amendments to the 2017 Plan increasing the shares available to grant. The 2017 Plan allows the Company, under the direction of the Compensation Committee of the Board of Directors, to make grants of restricted and 2018unrestricted stock awards to employees, consultants and directors. As of September 30, 2020, the Company may grant additional shares of common stock under the 2017 Plan with respect to the 0.1 options outstanding under our 2003 Plan and 4.8 options and restricted stock units outstanding under our 2010 Plan, to the extent that those options and restricted stock units expire or are cancelled without delivery of shares of common stock. If an RSU awarded under the 2017 Plan is cancelled or forfeited without the issuance of shares of common stock, the unissued or reacquired shares, which were subject to the RSU, shall again be available for issuance pursuant to the 2017 Plan.
The number of shares, terms, and vesting periods are determined by the Company’s Board of Directors or a committee thereof on an award-by-award basis. RSUs granted to employees generally vest ratably over four years on the anniversary date of the designated day of the last week of the month in which the RSUs are granted. The number of RSUs awarded to certain executive officers may be increased or reduced based on certain additional performance metrics. Options and RSUs granted to our non-employee directors vest in full upon completion of one year of service on the anniversary following the date of the grant. Options generally vest ratably over service periods of four years.  Options granted after December 5, 2012 expire eight years from the date of grant, and options granted prior to that date generally expire ten years from the date of grant. In September 2014, the Company began generally issuing RSUs in lieu of stock options.  
During the three months ended September 30, 2020, the Company granted stock-based awards to the Company's new President and Chief Executive Officer as an inducement material to his commencement of employment and entry into an employment agreement with the Company. The inducement awards were made in accordance with Nasdaq Stock Market rules and were not made under the Company's existing equity plans; the inducement awards are included in the tables below.

17

Table of Contents
Stock Options
A summary of the stock option activity under the Company’s equity plans, including the Company's inducement awards, for the three months ended September 30, 2020 is as follows:

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Shares purchased and retired

 

 

 

 

 

 

Common stock and additional paid-in-capital reductions

 

$

 

 

$

 

Charges to retained earnings

 

$

 

 

$

 

Number
of
shares
Weighted
average
exercise
price
Options outstanding at June 30, 20204.8 $24.47 
Options granted0.7 $13.38 
Less:
Options exercised$
Options canceled or expired(0.1)$16.40 
Options outstanding at September 30, 20205.4 $23.19 
Options exercisable at September 30, 20204.7 $24.62 

(11)

INCOME TAXES

As of September 30, 2020, there was $5.2 of unrecognized share-based compensation expense related to the inducement stock options that will be recognized over a weighted-average period of 2.8 years.

Restricted Stock Units
A summary of the RSU activity under the Company’s plans, including the Company's inducement awards and RSU awards with performance metrics, for the three months ended September 30, 2020 is as follows:
Number
of
shares
Weighted
average
grant date
fair value
RSUs outstanding at June 30, 20202.3 $32.50 
RSUs granted0.4 $13.24 
Less:
RSUs vested(0.8)$33.07 
RSUs canceled$
RSUs outstanding at September 30, 20201.9 $27.70 
As of September 30, 2020, there was $44.1 of total unrecognized share-based compensation expense related to RSUs that will be recognized over a weighted-average period of 2.5 years. 
Employee Stock Purchase Plan
The Company also has an Employee Stock Purchase Plan that was approved by shareholders in 2012 (the “2012 Purchase Plan”), under which 2.0 shares of common stock have been authorized.  Shares are issued under the 2012 Purchase Plan twice yearly at the end of each offering period.  As of September 30, 2020, approximately 0.3 shares of common stock are available for issuance under the 2012 Purchase Plan.
Share-Based Compensation Expense
Share-based compensation expense recognized and included in the condensed consolidated statements of operations and comprehensive loss was allocated as follows:
Three months ended
September 30,
20202019
Cost of molecular diagnostic testing$0.3 $0.2 
Cost of pharmaceutical and clinical services0.1 0.1 
Research and development expense1.3 1.5 
Selling, general, and administrative expense6.7 7.0 
     Total share-based compensation expense$8.4 $8.8 

18

Table of Contents
(12)INCOME TAXES
In order to determine the Company’s quarterly provision for income taxes, the Company used an estimated annual effective tax rate that is based on expected annual income and statutory tax rates in the various jurisdictions in which the Company operates. TheUnder the Tax Act Cuts and Jobs Act, reduces the federal corporate tax rate tois 21% for the fiscalcalendar year ending June 30, 2020. Certain significant or unusual items are separately recognized in the quarter during which they occur and can be a source of variability in the effective tax rate from quarter to quarter.   Certain significant or unusual items are separately recognized in the quarter during which they occur and can be a source of variability in the effective tax rate from quarter to quarter.

Income tax benefit for the three months ended September 30, 20192020 was $(1.7),$28.5, or approximately 65.2% of pre-tax loss compared to an income tax benefit of $1.7, or approximately 7.6% of pre-tax income compared to income tax expense of $1.6, or approximately 200.0% of pre-tax income,loss, for the three months ended September 30,

16


2018. 2019.  Income tax expensebenefit for the three months ended September 30, 20192020 is based on the Company’s estimated annualannualized effective tax rate for the full fiscal yearsix-month transition period ending June 30,December 31, 2020, adjusted by discrete items recognized during the period.  For the three months ended September 30, 2019,2020, the Company’s recognized effective tax rate differs from the U.S. federal statutory rate primarily due to carrying back net operating losses due to the effectCARES Act.

On March 27, 2020, the Coronavirus Aid, Relief, and Economic Security Act (“CARES”) was enacted.  CARES impacted several provisions to the U.S. tax code that have affected our six-month transition period ending December 31, 2020, including, but not limited to, (1) NOL carry-back and carry-forward provisions, (2) deductibility of interest, (3) acceleration of corporate AMT credits, and (4) classification of qualified improvement property.  As of the releasequarter ended September 30, 2020, the Company recognized an income tax net benefit of uncertain tax liabilities, state income taxes, acquisition transaction costs, and differences$20.0 related to the CARES Act, which included an increase in the uncertain tax effectbenefit accrual of equity compensation expense$14.3, related to carrying back net operating losses to tax years with higher corporate tax rates than the year the net operating loss originated. The Company will continue to evaluate the application of any and all provisions through the deduction realized when exercised, released or sold.

remainder of the six-month transition period ending December 31, 2020.

The Company files U.S., foreign and state income tax returns in jurisdictions with various statutes of limitations.  The Company is currently under audit by the state of New Jersey for the fiscal years June 30, 2013 through 2017; the state of New York and Massachusetts for the fiscal years June 30, 2014 through 2016; Germany for the fiscal years June 30, 2013 through 2015; and Switzerland for the fiscal years June 30, 2015 through 2016. Annual and interim tax provisions include amounts considered necessary to pay assessments that may result from examination of prior year tax returns; however, the amount ultimately paid upon resolution of issues may differ materially from the amount accrued.

(12)

SHARE-BASED COMPENSATION

On November 30, 2017, the Company’s shareholders approved the adoption of the 2017 Employee, Director and Consultant Equity Incentive Plan (the “2017 Plan”).

(13)COMMITMENTS AND CONTINGENCIES
The 2017 Plan allows the Company, under the direction of the Compensation Committee of the Board of Directors, to make grants of restricted and unrestricted stock awards to employees, consultants and directors. As of September 30, 2019, the Company may grant additional shares of common stock under the 2017 Plan with respect to the 0.4 options outstanding under our 2003 Plan and 5.3 options and restricted stock units outstanding under our 2010 Plan, that expire or are cancelled without delivery of shares of common stock. If an RSU awarded under the 2017 Plan is cancelled or forfeited without the issuance of shares of common stock, the unissued or reacquired shares, which were subject to the RSU, shall again be available for issuance pursuant to the 2017 Plan.

The number of shares, terms, and vesting periods are determined by the Company’s Board of Directors or a committee thereof on an option-by-option basis. Options generally vest ratably over service periods of four years.  Options granted after December 5, 2012 expire eight years from the date of grant, and options granted prior to that date generally expire ten years from the date of grant. In September 2014, the Company began issuing restricted stock units (“RSUs”) in lieu of stock options.  RSUs granted to employees generally vest ratably over four years on the anniversary date of the designated day of the last week of the month in which the RSUs are granted. The number of RSUs awarded to certain executive officers may be reduced if certain additional performance metrics are not met. Options and RSUs granted to our non-employee directors vest in full upon completion of one year of service on the Board following the date of the grant.

Stock Options

A summary of the stock option activity under the Company’s plans for the three months ended September 30, 2019 is as follows:

 

 

Number

of

shares

 

 

Weighted

average

exercise

price

 

Options outstanding at June 30, 2019

 

 

5.5

 

 

$

24.45

 

Options granted

 

 

 

 

$

 

Less:

 

 

 

 

 

 

 

 

Options exercised

 

 

(0.4

)

 

$

22.87

 

Options canceled or expired

 

 

(0.1

)

 

$

30.00

 

Options outstanding at September 30, 2019

 

 

5.0

 

 

$

24.39

 

Options exercisable at September 30, 2019

 

 

5.0

 

 

$

24.39

 

As of September 30, 2019, there was 0 unrecognized share-based compensation expense related to stock options.

Restricted Stock Units

A summary of the RSU activity under the Company’s plans for the three months ended September 30, 2019 is as follows:

17


 

 

Number

of

shares

 

 

Weighted

average

grant date

fair value

 

RSUs outstanding at June 30, 2019

 

 

2.4

 

 

$

37.70

 

RSUs granted

 

 

1.2

 

 

$

29.89

 

Less:

 

 

 

 

 

 

 

 

RSUs vested

 

 

(0.8

)

 

$

36.00

 

RSUs canceled

 

 

(0.1

)

 

$

46.00

 

RSUs outstanding at September 30, 2019

 

 

2.7

 

 

$

34.71

 

As of September 30, 2019, there was $39.2 of total unrecognized share-based compensation expense related to RSUs that will be recognized over a weighted-average period of 2.7 years.  This unrecognized compensation expense is equal to the fair value of RSUs expected to vest.

Employee Stock Purchase Plan

The Company also has an Employee Stock Purchase Plan that was approved by shareholders in 2012 (the “2012 Purchase Plan”), under which 2.0 shares of common stock have been authorized.  Shares are issued under the 2012 Purchase Plan twice yearly at the end of each offering period.  As of September 30, 2019, approximately 0.6 shares of common stock are available for issuance under the 2012 Purchase Plan.

Share-Based Compensation Expense

Share-based compensation expense recognized and included in the condensed consolidated statements of income and comprehensive income was allocated as follows:

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Cost of molecular diagnostic testing

 

$

0.2

 

 

$

0.2

 

Cost of pharmaceutical and clinical services

 

 

0.1

 

 

 

0.1

 

Research and development expense

 

 

1.5

 

 

 

1.2

 

Selling, general, and administrative expense

 

 

7.0

 

 

 

6.2

 

Total share-based compensation expense

 

$

8.8

 

 

$

7.7

 

(13)

FAIR VALUE MEASUREMENTS

The fair value of the Company’s financial instruments reflects the amounts that the Company estimates it will receive in connection with the sale of an asset or pay in connection with the transfer of a liability in an orderly transaction between market participants at the measurement date (exit price). The fair value of contingent consideration related to the Sividon and Assurex acquisitions as well as the long-term debt were categorized as a level 3 liability, as the measurement amount is based primarily on significant inputs not observable in the market. The fair value hierarchy prioritizes the use of inputs used in valuation techniques into the following three levels:

Level 1—quoted prices in active markets for identical assets and liabilities.

Level 2—observable inputs other than quoted prices in active markets for identical assets and liabilities; quoted prices in markets that are not active; or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities.  Some of the Company’s marketable securities primarily utilize broker quotes in a non-active market for valuation of these securities.

Level 3—unobservable inputs.

18


All of the Company’s financial instruments are valued using quoted prices in active markets or based on other observable inputs.  For Level 2 securities, the Company uses a third party pricing service which provides documentation on an ongoing basis that includes, among other things, pricing information with respect to reference data, methodology, inputs summarized by asset class, pricing application and corroborative information.  For Level 3 contingent consideration, the Company reassesses the fair value of expected contingent consideration and the corresponding liability each reporting period using the Monte Carlo Method, which is consistent with the initial measurement of the expected earn out liability.  This fair value measurement is considered a Level 3 measurement because the Company estimates projections during the earn out period utilizing various potential pay-out scenarios.  Probabilities were applied to each potential scenario and the resulting values were discounted using a rate that considers weighted average cost of capital as well as a specific risk premium associated with the riskiness of the earn-out itself, the related projections, and the overall business.  The contingent earn-out liabilities are classified as a component of long-term and short-term contingent consideration in the Company’s consolidated balance sheets.  Changes to the earn-out liabilities are reflected in change in the fair value of contingent consideration in our consolidated statements of operations. Changes to the unobservable inputs could have a material impact on the Company’s financial statements.

The fair value of our long-term debt, which we consider a Level 3 measurement, is estimated using discounted cash flow analyses, based on the Company’s current estimated incremental borrowing rates for similar borrowing arrangements.  The fair value of long-term debt is estimated to be $224.7 at September 30, 2019.

The following table sets forth the fair value of the financial assets and liabilities that the Company re-measures on a regular basis:

 

 

Level 1

 

 

Level 2

 

 

Level 3

 

 

Total

 

September 30, 2019

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Money market funds (a)

 

$

13.3

 

 

$

 

 

$

 

 

$

13.3

 

Corporate bonds and notes

 

 

1.5

 

 

 

69.1

 

 

 

 

 

 

70.6

 

Municipal bonds

 

 

 

 

 

15.1

 

 

 

 

 

 

15.1

 

Federal agency issues

 

 

 

 

 

7.0

 

 

 

 

 

 

7.0

 

US government securities

 

 

 

 

 

13.0

 

 

 

 

 

 

13.0

 

Contingent consideration

 

 

 

 

 

 

 

 

(10.7

)

 

 

(10.7

)

Total

 

$

14.8

 

 

$

104.2

 

 

$

(10.7

)

 

$

108.3

 

(a)

Money market funds are primarily comprised of exchange traded funds and accrued interest.

 

 

Level 1

 

 

Level 2

 

 

Level 3

 

 

Total

 

June 30, 2019

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Money market funds (a)

 

$

17.2

 

 

$

 

 

$

 

 

$

17.2

 

Corporate bonds and notes

 

 

2.5

 

 

 

64.4

 

 

 

 

 

 

66.9

 

Municipal bonds

 

 

 

 

 

15.4

 

 

 

 

 

 

15.4

 

Federal agency issues

 

 

 

 

 

9.0

 

 

 

 

 

 

9.0

 

US government securities

 

 

 

 

 

9.8

 

 

 

 

 

 

9.8

 

Contingent consideration

 

 

 

 

 

 

 

 

(13.8

)

 

 

(13.8

)

Total

 

$

19.7

 

 

$

98.6

 

 

$

(13.8

)

 

$

104.5

 

(a)

Money market funds are primarily comprised of exchange traded funds and accrued interest.

The following table reconciles the change in the fair value of the contingent consideration during the periods presented:

 

 

Carrying

amount

 

Balance June 30, 2019

 

$

13.8

 

Payment of contingent consideration

 

 

(3.3

)

Change in fair value recognized in the income statement

 

 

(0.7

)

Translation adjustments recognized in other comprehensive income

 

 

0.9

 

Ending balance September 30, 2019

 

$

10.7

 

19


(14)

COMMITMENTS AND CONTINGENCIES

In July 2019, the Company resolved the complaint filed by a qui tam relator in October 2017 in the United States District Court for the District of South Carolina.  The complaint was the basis of the Office of Inspector General (OIG) subpoena dated February 2018 regarding Medicare billing practices relating to the Company’s hereditary cancer testing from 2014 to 2018.  After a 17-month investigation, the Department of Justice declined to intervene in the case.  The Company believes this demonstrated that the key allegations made in the complaint were false.  In order to avoid a lengthy and distracting litigation with the qui tam relator, the Company entered into a settlement agreement on July 18, 2019 under which the Company would pay $9.1 to the qui tam relator in order to settle the matter. The Company paid the settlement amount of $9.1 in October 2019. The Company denies any wrongdoing and does not anticipate any material change in its billing practices.

In addition, the Company is subject to various claims and legal proceedings covering matters that arise in the ordinary course of its business activities. As of September 30, 2019,2020, the management of the Company believes any reasonably possible liability that may result from the resolution of these matters will not have a material adverse effect on the Company’s consolidated financial position, operating results, or cash flows.

From time to time, the Company receives recoupment requests from third-party payors for alleged overpayments. The Company leases certain office spaces and research and development laboratory facilities, vehicles, and office equipmentdisagrees with remaining lease terms ranging from one to six years. These leases require monthly lease payments that may be subject to annual increases throughout the lease term. Certain of these leases also include renewal options which allows the Company to, at its election, renew or extend the lease for a fixed or indefinite period of time. These optional periods have not been considered in the determinationcontentions of the right-of-use-assetspending requests or lease liabilities associated with these leases ashas recorded an estimated reserve for the Company did not consider it reasonably certain it would exercise the options.

The Company performed evaluations of its contracts and determined each of its identified leases are operating leases. For the three months ended September 30, 2019, the Company incurred $4.6 in lease costs which are included in operating expenses in the consolidated statement of operations in relation to these operating leases. Of such lease costs, $0.6 was variable lease expense and $0.1 was short-term lease expense, and neither of them were included in the measurement of the Company's operating ROU assets and lease liabilities. The variable rent expense is comprised primarily of the Company's proportionate share of operating expenses, property taxes, and insurance and is classified as lease expense due to the Company's election to not separate lease and non-lease components.

As of September 30, 2019, the maturities of the Company’s operating lease liabilities were as follows:

alleged overpayments.

Fiscal year ending:

 

 

 

 

2020

 

$

11.9

 

2021

 

 

14.9

 

2022

 

 

13.7

 

2023

 

 

12.6

 

2024

 

 

12.3

 

Thereafter

 

 

19.3

 

Total lease payments

 

$

84.7

 

As of September 30, 2019, the weighted average remaining lease term is 6.0 years and the weighted average discount rate used to determine the operating lease liability was 3.87%.

Disclosures related to periods prior to the adoption of ASU 2016-02

The following table summarizes the future minimum lease payments as of June 30, 2019:

Fiscal year ending:

 

 

 

 

2020

 

$

15.1

 

2021

 

 

14.1

 

2022

 

 

13.1

 

2023

 

 

12.2

 

2024

 

 

11.9

 

Thereafter

 

 

19.1

 

Total lease payments

 

$

85.5

 

(14)     SEGMENT AND RELATED INFORMATION

20


(15)

EMPLOYEE DEFERRED SAVINGS PLAN

The Company has a deferred savings plan which qualifies under Section 401(k) of the Internal Revenue Code. Substantially all of the Company’s U.S. employees are covered by the plan. The Company makes matching contributions of 50% of each employee’s contribution with the employer’s contribution not to exceed 4% of the employee’s compensation. The Company recorded contributions to the plan as follows:

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Deferred savings plan contributions

 

$

2.5

 

 

$

2.0

 

(16)

SEGMENT AND RELATED INFORMATION

The Company’s business is aligned with how the Chief Operating Decision Makerchief operating decision maker reviews performance and makes decisions in managing the Company.  The business units have been aggregated into 2 reportable segments: (i) diagnostics and (ii) other. The diagnostics segment provides testing and collaborative development of testing that is designed to assess an individual’s risk for developing disease later in life, identify a patient’s likelihood of responding to drug therapy and guide a patient’s dosing to ensure optimal treatment, or assess a patient’s risk of disease progression and disease recurrence. The other segment provides testing products and services to the pharmaceutical, biotechnology and medical research industries, research and development, and clinical services for patients, and includes corporate services such as finance, human resources, legal and information technology.


19

Table of Contents
Segment revenue and operating income (loss) were as follows during the periods presented:

 

Diagnostics

 

 

Other

 

 

Total

 

DiagnosticsOtherTotal
Three months ended September 30, 2020Three months ended September 30, 2020
RevenuesRevenues$130.5 $14.7 $145.2 
Depreciation and amortizationDepreciation and amortization16.7 1.0 17.7 
Segment operating lossSegment operating loss(0.3)(39.3)(39.6)

Three months ended September 30, 2019

 

 

 

 

 

 

 

 

 

 

 

 

Three months ended September 30, 2019

Revenues

 

$

170.4

 

 

$

15.9

 

 

$

186.3

 

Revenues$170.4 $15.9 $186.3 

Depreciation and amortization

 

 

16.9

 

 

 

1.3

 

 

 

18.2

 

Depreciation and amortization16.9 1.3 18.2 

Segment operating income (loss)

 

 

17.3

 

 

 

(38.2

)

 

 

(20.9

)

Segment operating income (loss)17.3 (38.2)(20.9)

Three months ended September 30, 2018

 

 

 

 

 

 

 

 

 

 

 

 

Revenues

 

$

189.0

 

 

$

13.3

 

 

$

202.3

 

Depreciation and amortization

 

 

17.0

 

 

 

1.3

 

 

 

18.3

 

Segment operating income

 

 

27.6

 

 

 

(26.4

)

 

 

1.2

 

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Total operating income for reportable segments

 

$

(20.9

)

 

$

1.2

 

Unallocated amounts:

 

 

 

 

 

 

 

 

Interest income

 

 

0.9

 

 

 

0.7

 

Interest expense

 

 

(2.9

)

 

 

(2.2

)

Other

 

 

0.6

 

 

 

1.1

 

Income (loss) from operations before income taxes

 

 

(22.3

)

 

 

0.8

 

Income tax provision

 

 

(1.7

)

 

 

1.6

 

Net income (loss)

 

 

(20.6

)

 

 

(0.8

)

Net loss attributable to non-controlling interest

 

 

 

 

 

(0.1

)

Net income (loss) attributable to Myriad Genetics, Inc.

   stockholders

 

$

(20.6

)

 

$

(0.7

)


21

Three months ended
September 30,
20202019
Total operating loss for reportable segments$(39.6)$(20.9)
Unallocated amounts:
Interest income0.4 0.9 
Interest expense(2.9)(2.9)
Other(1.6)0.6 
Loss from operations before income taxes(43.7)(22.3)
Income tax benefit(28.5)(1.7)
Net loss(15.2)(20.6)
Net loss attributable to non-controlling interest
Net loss attributable to Myriad Genetics, Inc. stockholders$(15.2)$(20.6)

(15)    SUPPLEMENTAL CASH FLOW INFORMATION
Three months ended
September 30,
20202019
Cash paid during the period for income taxes$1.3 $0.2 
Cash paid for interest2.6 2.8 
Establishment of operating lease right-of-use assets and lease liabilities
Operating lease right-of-use assets$— $74.5 
Operating lease liabilities— (78.8)
Accrued liabilities and other long-term liabilities— 4.3 

(16)     SUBSEQUENT EVENTS
Change in Fiscal Year
On October 9, 2020, the Company’s Board of Directors approved a change in the Company’s fiscal year from a fiscal year ending on the last day of June of each year to a calendar fiscal year ending on the last day of December of each year, effective January 1, 2021. Accordingly, the Company will be issuing financial statements for a six-month transition period ending December 31, 2020 and calendar year financial statements thereafter.
20

(17)


SUPPLEMENTAL CASH FLOW INFORMATION

 

 

Three months ended

 

 

 

September 30,

 

 

 

2019

 

 

2018

 

Cash paid during the period for income taxes

 

$

0.2

 

 

$

4.9

 

Cash paid for interest

 

 

2.8

 

 

 

0.9

 

Establishment of operating lease right-of-use assets and

   lease liabilities

 

 

 

 

 

 

 

 

Operating lease right-of-use assets

 

$

74.5

 

 

$

 

Operating lease liabilities

 

 

(78.8

)

 

 

 

Accrued liabilities and other long-term liabilities

 

 

4.3

 

 

 

 


22


Item 2.    Management’s Discussion and Analysis of Financial Condition and Results of Operations

General

We are a leading precision medicine company acting as a trusted advisor to transform patient lives through pioneering molecular diagnostics. Through our proprietary technologies, we believe we are positioned to identify important disease genes, the proteins they produce,

(Dollars and the biological pathwaysshares in which such genes and proteins are involved to better understand the genetic basis of certain human diseases. We believe that identifying these biomarkers (i.e., DNA, RNA and proteins) will enable us to develop novel molecular diagnostic tests that can provide important information to solve unmet medical needs. During the three months ended September 30, 2019, we reported total revenues of $186.3 million and net loss of $20.6 million that included income tax benefit of $(1.7) million resulting in $(0.28) diluted earningsmillions, except per share.  

Our business units have been aligned with how the Chief Operating Decision Maker reviews performance and makes decisions in managing the Company.  The business units have been aggregated into two reportable segments: (i) diagnostics and (ii) other. The diagnostics segment provides testing and collaborative development of testing that is designed to assess an individual’s risk for developing disease later in life, identify a patient’s likelihood of responding to drug therapy and guide a patient’s dosing to ensure optimal treatment, or assess a patient’s risk of disease progression and disease recurrence. The other segment provides testing products and services to the pharmaceutical, biotechnology and medical research industries, research and development, and clinical services for patients, and includes corporate services such as finance, human resources, legal and information technology.

Business Highlights

During the quarter ended September 30, 2019, Myriad reduced its financial guidance based primarily on a reduction in its outlook for hereditary cancer revenue. The reduction is based upon a coding transition which reduced reimbursement for the Company’s hereditary cancer tests despite double digit volume growth in the fiscal first-quarter. For GeneSight, the Company received reimbursement coverage for the test from UnitedHealthcare, the largest commercial insurer in the country, which took effect on October 1, 2019. Additionally, Myriad signed a master service agreement with a large pharmacy benefit manager in the United States to offer GeneSight to commercial payer and self-funded employer customers. A Fortune 50 company has already opted into the master service agreement.

We also saw the publication of the precision medicine analysis from the GUIDED study which demonstrated the test statistically significantly improved remission, response rates, and symptoms in patients taking medication with predicted gene drug interactions. For the prenatal tests Myriad published a study on its NIPS test Prequel which demonstrated Prequel is the only commercial product that is highly accurate in women with high body mass index. With Prolaris, the company published a clinical utility study demonstrating 82 percent of men with low Prolaris scores choose active surveillance as initial treatment with 64% these men remaining on active surveillance after four years of follow up.

From a companion diagnostic perspective, Myriad filed a supplementary Premarket Approval Application with the U.S. Food and Drug Administration (FDA) to authorize BRACAnalysis CDx as a companion diagnostic test for olaparib in metastatic, castrate-resistant, prostate cancer patients with germline BRCA mutations. The company also received the first FDA approval for myChoice CDx® as a companion diagnostic by healthcare professionals to identify women with ovarian cancer who have homologous recombination deficiency and may be candidates for niraparib monotherapy in the fourth-line setting. The company plans to seek ADLT status for this test and has a list price of $4,040. Myriad also submitted the myChoice CDx® companion diagnostic test for approval by Japan’s Pharmaceuticals and Medical Devices Agency (PMDA) in parallel with Takeda’s PMDA review of the novel PARP inhibitor, niraparib.  Takeda has an exclusive licensing agreement to develop and commercialize niraparib in Japan.

Results of Operations for the Three Months Ended September 30, 2019 and 2018

Revenue

 

 

Three months ended

 

 

 

 

 

 

 

September 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

Revenue

 

$

186.3

 

 

$

202.3

 

 

$

(16.0

)

The decrease in revenue was primarily due to a reduction of $11.8 million in Hereditary Cancer Testing revenue due to reduced reimbursement, including changes in estimates for tests in which the performance obligation of delivering the test results was met in prior periods, and a reduction of $6.6 million in GeneSight revenue due to reduced volumes. These decreases were partially offset by an increase of $5.4 million in Prenatal revenue due to Counsyl contributing revenue for only a portion of the three months ended September 30, 2018 compared to the full three months ended September 30, 2019.

23


The following table presents additional detail regarding the composition of our total revenue for the three months ended September 30, 2019 and 2018:

 

 

Three months ended

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

September 30,

 

 

$

 

 

% of Total Revenue

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

 

2019

 

 

2018

 

Molecular diagnostic revenues:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Hereditary Cancer Testing

 

$

104.5

 

 

$

116.3

 

 

$

(11.8

)

 

 

56

%

 

 

57

%

GeneSight

 

 

22.7

 

 

 

29.3

 

 

 

(6.6

)

 

 

12

%

 

 

14

%

Prenatal

 

 

23.5

 

 

 

18.1

 

 

 

5.4

 

 

 

13

%

 

 

9

%

VectraDA

 

 

11.0

 

 

 

13.0

 

 

 

(2.0

)

 

 

6

%

 

 

6

%

Prolaris

 

 

6.5

 

 

 

6.2

 

 

 

0.3

 

 

 

3

%

 

 

3

%

EndoPredict

 

 

2.3

 

 

 

2.4

 

 

 

(0.1

)

 

 

1

%

 

 

1

%

Other

 

 

1.5

 

 

 

3.7

 

 

 

(2.2

)

 

 

1

%

 

 

2

%

Total molecular diagnostic revenue

 

 

172.0

 

 

 

189.0

 

 

 

(17.0

)

 

 

 

 

 

 

 

 

Pharmaceutical and clinical service revenue

 

 

14.3

 

 

 

13.3

 

 

 

1.0

 

 

 

8

%

 

 

8

%

Total revenue

 

$

186.3

 

 

$

202.3

 

 

$

(16.0

)

 

 

100

%

 

 

100

%

Cost of Sales

 

 

Three months ended

 

 

 

 

 

 

 

September 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

Cost of sales

 

$

49.7

 

 

$

49.7

 

 

$

 

Cost of sales as a % of sales

 

 

26.7

%

 

 

24.6

%

 

 

 

 

Cost of sales as a percentage of revenue increased from 24.6% to 26.7% during the three months ended September 30, 2019 compared to the same period in the prior year.  The increase was primarily driven by lower gross margins associated with the Counsyl business and reduction of reimbursement related to Hereditary Cancer and GeneSight, partially offset by the implementation of efficiency programs in our DNA, RNA, and protein based laboratories.

Research and Development Expenses

 

 

Three months ended

 

 

 

 

 

 

 

September 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

R&D expense

 

$

21.3

 

 

$

21.1

 

 

$

0.2

 

R&D expense as a % of sales

 

 

11.4

%

 

 

10.4

%

 

 

 

 

Research and development expense for the three months ended September 30, 2019 increased compared to the same period in the prior year primarily related to Counsyl being included for a full quarter during the quarter ended September 30, 2019 compared to only a partial quarter for the quarter ended September 30, 2018.

Change in the Fair Value of Contingent Consideration

 

 

Three months ended

 

 

 

 

 

 

 

September 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

Change in the fair value of contingent consideration

 

$

0.7

 

 

$

0.4

 

 

$

0.3

 

Change in the fair value of contingent consideration as a % of sales

 

 

0.4

%

 

 

0.2

%

 

 

 

 

24


The fair value of contingent consideration for the three months ended September 30, 2019 increased compared to the same period in the prior year due to increase in the fair value of contingent consideration related to the Sividon acquisition.  

Selling, General and Administrative Expenses

 

 

Three months ended

 

 

 

 

 

 

 

September 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

SG&A expense

 

$

135.5

 

 

$

129.9

 

 

$

5.6

 

SG&A expense as a % of sales

 

 

72.7

%

 

 

64.2

%

 

 

 

 

Selling, general and administrative expense increased slightly for the three months ended September 30, 2019 compared to the same period in the prior year primarily related to Counsyl being included for a full quarter during the quarter ended September 30, 2019 compared to only a partial quarter for the quarter ended September 30, 2018.

Other Income (Expense)

 

 

Three months ended

 

 

 

 

 

 

 

September 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

Other income (expense)

 

$

(1.4

)

 

$

(0.4

)

 

$

(1.0

)

For the three months ended September 30, 2019 compared to the same period in the prior year, the change in other income expense was primarily driven by an increase in interest expense related to the debt incurred to fund the acquisition of Counsyl.  This was partially offset by increased interest income.

Income Tax Expense

 

 

Three months ended

 

 

 

 

 

 

 

September 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

Income tax expense (benefit)

 

$

(1.7

)

 

$

1.6

 

 

$

(3.3

)

Effective tax rate

 

 

7.6

%

 

 

200.0

%

 

 

 

 

Our tax rate is the product of a blended U.S. federal effective rate of 21% and a blended state income tax rate of approximately 3%. Certain significant or unusual items are separately recognized during the period in which they occur and can be a source of variability in the effective tax rates from period to period.

Income tax benefit for the three months ended September 30, 2019 is $(1.7) million for an effective tax rate of 7.6%.  The decrease in the effective rate for the three months ended September 30, 2019 as compared to the same period in prior year is due to the release of uncertain tax liabilities, state income taxes, acquisition transaction cost, and the differences related to the tax effect of equity compensation expense and the deduction realized when exercised, released or sold.

Liquidity and Capital Resources

We believe that our existing capital resources and the cash to be generated from future sales will be sufficient to meet our projected operating requirements, including contingent consideration and repayment of the outstanding Facility, which matures on July 31, 2023, for the foreseeable future. There are no scheduled principal payments of the Facility prior to its maturity date; however, our available capital resources may be consumed more rapidly than currently expected and we may need or want to raise additional financing. We may not be able to secure such financing in a timely manner or on favorable terms, if at all.  Without additional funds, we may be forced to delay, scale back or eliminate some of our sales and marketing efforts, research and development activities, or other operations and potentially delay development of our diagnostic tests in an effort to provide sufficient funds to continue our operations. If any of these events occurs, our ability to achieve our development and commercialization goals would be adversely affected.

Our capital deployment strategy focuses on use of resources in three key areas: research and development, acquisitions and the repurchase of our common stock.  We believe that research and development provides the best return on invested capital.  We also allocate capital for acquisitions that support our business strategy and share repurchases based on business and market conditions.

25


The following table represents the balances of cash, cash equivalents and marketable investment securities:

data)

 

 

September 30,

 

 

June 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2019

 

 

Change

 

Cash and cash equivalents

 

$

89.9

 

 

$

93.2

 

 

$

(3.3

)

Marketable investment securities

 

 

52.7

 

 

 

43.7

 

 

 

9.0

 

Long-term marketable investment securities

 

 

51.5

 

 

 

54.9

 

 

 

(3.4

)

Cash, cash equivalents and marketable investment

   securities

 

$

194.1

 

 

$

191.8

 

 

$

2.3

 

The decrease in cash and cash equivalents was primarily driven by the repayment of principle on the Amended Facility of $8.6 million, the payment of contingent consideration of $3.3 million related to Sividon, and $18.8 million reduction in net income excluding the change in the fair value of contingent consideration.  This was partially offset by $15.8 million in cash provided by operating activities.

The following table represents the condensed consolidated cash flow statement:

 

 

Three months ended

 

 

 

 

 

 

 

September 30,

 

 

 

 

 

(In millions)

 

2019

 

 

2018

 

 

Change

 

Cash flows from operating activities

 

$

15.8

 

 

 

7.8

 

 

$

8.0

 

Cash flows from investing activities

 

 

(7.1

)

 

 

(279.0

)

 

 

271.9

 

Cash flows from financing activities

 

 

(12.3

)

 

 

252.1

 

 

 

(264.4

)

Effect of foreign exchange rates on cash and cash equivalents

 

 

0.3

 

 

 

1.5

 

 

 

(1.2

)

Net increase (decrease) in cash and cash equivalents

 

 

(3.3

)

 

 

(17.6

)

 

 

14.3

 

Cash and cash equivalents at the beginning  of the year

 

 

93.2

 

 

 

110.9

 

 

 

(17.7

)

Cash and cash equivalents at the end  of the period

 

$

89.9

 

 

$

93.3

 

 

$

(3.4

)

Forward-Looking Statements

Cash Flows from Operating Activities

The increase in cash flows from operating activities for the three months ended September 30, 2019, compared to the same period in the prior year, was primarily due to a $28.3 million change in assets and liabilities associated with operating activities, partially offset by a $18.8 million decrease in net income excluding contingent consideration.  

Cash Flows from Investing Activities

For the three months ended September 30, 2019, compared to the same period in the prior year, the increase in cash used in investing activities was driven primarily by the $279.6 million used for the acquisition of Counsyl that occurred during the same period in the prior year.  This was partially offset by a $7.6 million increase in net purchases of marketable investment securities.

Cash Flows from Financing Activities

For the three months ended September 30, 2019, compared to the same period in the prior year, the decrease in cash flows from financing activities was driven primarily by the $290.0 million in net proceeds from the revolving credit facility that occurred during the same period in the prior year but did not occur during the three months ended September 30, 2019.  The decrease in cash flows were partially offset by only $8.6 million in cash paid for repayment of the revolving credit facility during the three months ended September 30, 2019 compared to $40.0 million in cash paid for repayment of the revolving credit facility during the same period in the prior year.

Effects of Inflation

We do not believe that inflation has had a material impact on our business, sales, or operating results during the periods presented.

Share Repurchase Program

In June 2016, our Board of Directors authorized an eighth share repurchase program of $200.0 million of our outstanding common stock. We plan to repurchase our common stock from time to time or on an accelerated basis through open market transactions or privately negotiated transactions as determined by our management. The amount and timing of stock repurchases under the program will depend on business and market conditions, stock price, trading restrictions, acquisition activity and other factors.  As of September 30, 2019, we have $110.7 million remaining on our current share repurchase authorization.  See also “Part II, Item 2. Unregistered Sales of Equity Securities and Use of Proceeds – Issuer Purchases of Equity Securities”.

26


Critical Accounting Policies

Critical accounting policies are those policies which are both important to the presentation of a company’s financial condition and results and require management’s most difficult, subjective or complex judgments, often as a result of the need to make estimates about the effect of matters that are inherently uncertain.  During the first quarter of fiscal 2019, we adopted new accounting guidance related to lease accounting, which is described above at “Recent Accounting Pronouncements.” There have been no other significant changes to our accounting policies during the period.  For a further discussion of our critical accounting policies, see our Annual Report on Form 10-K for the fiscal year ended June 30, 2019.

Certain Factors That May Affect Future Results of Operations

The Securities and Exchange Commission encourages companies to disclose forward-looking information so that investors can better understand a company’s future prospects and make informed investment decisions. This Quarterly Report on Form 10-Q contains such “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995.

Words such as “may,” “anticipate,” “estimate,” “expects,” “projects,” “intends,” “plans,” “believes,” “potential,“seek,” “could,” “would,” “continue,” “likely,” “will,” “strategy,“strategy”, “goal” and words and terms of similar substance used in connection with any discussion of future operating or financial performance, identify forward-looking statements. All forward-looking statements are management’s present expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those described in the forward-looking statements. These risks include, but are not limited to: uncertainties associated with COVID-19, including its possible effects on our operations and the demand for our products and services; our ability to efficiently and flexibly manage our business amid uncertainties related to COVID-19; the risk that sales and profit margins of our existing molecular diagnostic tests and pharmaceutical and clinical services may decline or will not continue to increase at historical rates; risks related to our ability to successfully transition from our existing product portfolio to our new tests; risks related to changes in the governmental or private insurers’ coverage and reimbursement levels for our tests or our ability to obtain reimbursement for our new tests at comparable levels to our existing tests; risks related to increased competition and the development of new competing tests and services; the risk that we may be unable to develop or achieve commercial success for additional molecular diagnostic tests and pharmaceutical and clinical services in a timely manner, or at all; the risk that we may not successfully develop new markets for our molecular diagnostic tests and pharmaceutical and clinical services, including our ability to successfully generate revenue outside the United States; the risk that licenses to the technology underlying our molecular diagnostic tests and pharmaceutical and clinical services tests and any future tests are terminated or cannot be maintained on satisfactory terms; risks related to delays or other problems with operating our laboratory testing facilities; risks related to public concern over our genetic testing in general or our tests in particular; risks related to regulatory requirements or enforcement in the United States and foreign countries and changes in the structure of the healthcare system or healthcare payment systems; risks related to our ability to obtain new corporate collaborations or licenses and acquire new technologies or businesses on satisfactory terms, if at all; risks related to our ability to successfully integrate and derive benefits from any technologies or businesses that we license or acquire, including but not limited to our acquisition of Counsyl, Assurex, Crescendo, Sividon and the Clinic;acquire; risks related to our projections about the potential market opportunity for our products; the risk that we or our licensors may be unable to protect or that third parties will infringe the proprietary technologies underlying our tests; the risk of patent-infringement claims or challenges to the validity of our patents; risks related to changes in intellectual property laws covering our molecular diagnostic tests and pharmaceutical and clinical services and patents or enforcement in the United States and foreign countries, such as the Supreme Court decisiondecisions in the lawsuit brought against us by the AssociationMayo Collab. Servs. v. Prometheus Labs., Inc., 566 U.S. 66 (2012), Ass’n for Molecular Pathology et al;v. Myriad Genetics, Inc., 569 U.S. 576 (2013), and Alice Corp. v. CLS Bank Int’l, 573 U.S. 208 (2014); risks of new, changing and competitive technologies and regulations in the United States and internationally; the risk that we may be unable to comply with financial operating covenants under our credit or lending agreements:agreements; the risk that we will be unable to pay, when due, amounts due under our creditorcredit or lending agreements; and other factors discussed under the heading “Risk Factors” contained in Item 1A of our Annual report on Form 10-K for the fiscal year ended June 30, 2019,2020, which has been filed with the Securities and Exchange Commission, as well as any updates to those risk factors filed from time to time in our Quarterly Reports on Form 10-Q (including Item 1A below in this report) or Current Reports on Form 8-K.

In light of these assumptions, risks and uncertainties, the results and events discussed in the forward-looking statements contained in this Quarterly Report or in any document incorporated by reference might not occur. Stockholders are cautioned not to place undue reliance on the forward-looking statements, which speak only as of the date of this Quarterly Report. We are not under any obligation, and we expressly disclaim any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events or otherwise. All subsequent forward-looking statements attributable to us or to any person acting on our behalf are expressly qualified in their entirety by the cautionary statements contained or referred to in this section.

27



21


General
We are a leading precision medicine company acting as a trusted advisor to transform patient lives through pioneering molecular diagnostics. Through our proprietary technologies, we believe we are positioned to identify important disease genes, the proteins they produce, and the biological pathways in which such genes and proteins are involved to better understand the molecular basis of certain human diseases. We believe that identifying these biomarkers (i.e., DNA, RNA and proteins) will enable us to develop novel molecular diagnostic tests that can provide important information to solve unmet medical needs. During the three months ended September 30, 2020, we reported total revenues of $145.2 and net loss of $(15.2) resulting in $(0.20) net loss per share.
Our business units have been aligned with how the chief operating decision maker reviews performance and makes decisions in managing the Company. The business units have been aggregated into two reportable segments: (i) diagnostics and (ii) other. The diagnostics segment provides testing and collaborative development of testing that is designed to assess an individual’s risk for developing disease later in life, identify a patient’s likelihood of responding to drug therapy and guide a patient’s dosing to ensure optimal treatment, or assess a patient’s risk of disease progression and disease recurrence. The other segment provides testing products and services to the pharmaceutical, biotechnology and medical research industries, research and development, and clinical services for patients, and includes corporate services such as finance, human resources, legal and information technology.
Business Updates

During the quarter ended September 30, 2020, we continued to see improvement in business fundamentals, including test volumes, for our diagnostic products which have been affected by the COVID-19 pandemic. Total test volumes reached 90 percent of pre-pandemic levels by the end of the quarter compared to 75 percent of pre-pandemic levels at the end of the prior quarter ended June 30, 2020. We have also made the following recent announcements:

Appointed Paul J. Diaz as President and Chief Executive Officer, effective August 13, 2020.

The American College of Obstetricians and Gynecologists recently issued guidelines recommending prenatal testing for average risk patients. These guidelines have led to new medical policy guidelines for payors covering average risk testing incorporating 24 million covered lives to date.

Received a local coverage determination ("LCD") for Prolaris for unfavorable intermediate and high-risk patients from Palmetto GBA and CGS Administrators, LLC, two of the administrative contractors for the Centers for Medicare & Medicaid Services. The final LCD becomes effective December 6, 2020.

The final LCD for pharmacogenomic (PGx) testing became effective during the quarter, which expanded coverage for patients to all healthcare providers licensed and qualified to diagnose the condition and prescribe relevant medications (either independently or in an arrangement).

Received coverage from the German Federal Joint Committee (G-BA) for the EndoPredict® breast cancer prognostic test. The positive decision means that EndoPredict® is now available to all patients with statutory health insurance in Germany without restrictions as a benefit of the statutory health insurance scheme (GKV).

Change in Fiscal Year
On October 9, 2020, our Board of Directors approved a change in our fiscal year from a fiscal year ending on the last day of June of each year to a calendar fiscal year ending on the last day of December of each year, effective January 1, 2021. Accordingly, we will be issuing financial statements for a six-month transition period ending as of December 31, 2020, and calendar year financial statements thereafter.

22


Results of Operations for the Three Months Ended September 30, 2020 and 2019
Revenue
Three months ended September 30,
(In millions)20202019Change
Revenue$145.2 $186.3 $(41.1)
The Company's revenues for the three months ended September 30, 2020 continued to be impacted by factors related to the COVID-19 pandemic, including patients incurring obstacles to access healthcare professionals, which resulted in testing volumes declining compared to the prior year across the majority of the products. In addition, the average expected reimbursement per test decreased due to a variety of factors such as negotiating new contracts with payors and the impact of a $2.2 million reduction in revenues for estimated future refunds across the Company's products. Hereditary Cancer Testing revenues decreased $23.9 compared to the same period in the prior year due primarily to an approximate 18% decrease in volumes and an approximate 6% decrease in average reimbursement per test. GeneSight revenues declined $10.8 compared to the same period in the prior year due primarily to an approximate 28% decrease in volumes and an approximate 27% decrease in average reimbursement per test. Prenatal revenues declined $7.0 compared to the same period in the prior year due primarily to a decrease in average reimbursement per test of approximately 34%. Pharmaceutical and clinical service revenue declined $4.8 compared to the same period in the prior year, primarily as a result of selling the Clinic in February 2020.
The following table presents additional detail regarding the composition of our total revenue for the three months ended September 30, 2020 and 2019:
Three months ended September 30,$
Change
% of Total Revenue
(In millions)2020201920202019
Molecular diagnostic revenues:
Hereditary Cancer Testing$80.6 $104.5 $(23.9)56 %56 %
Prenatal16.5 23.5 (7.0)11 %13 %
GeneSight11.9 22.7 (10.8)%12 %
Vectra9.1 11.0 (1.9)%%
myChoice CDx7.8 1.3 6.5 %%
Prolaris6.4 6.5 (0.1)%%
EndoPredict2.8 2.3 0.5 %%
Other0.6 0.2 0.4 — %— %
Total molecular diagnostic revenue135.7 172.0 (36.3)
Pharmaceutical and clinical service revenue9.5 14.3 (4.8)%%
Total revenue$145.2 $186.3 $(41.1)100 %100 %
Cost of Sales
Three months ended September 30,
(In millions)20202019Change
Cost of molecular diagnostic testing$39.9 $41.2 $(1.3)
Cost of molecular diagnostic testing as a % of revenue29.4 %24.0 %
Cost of pharmaceutical and clinical services$4.3 $8.5 $(4.2)
Cost of pharmaceutical and clinical services as a % of revenue45.3 %59.4 %
The cost of molecular diagnostic testing as a percentage of revenue increased from 24.0% to 29.4% during the three months ended September 30, 2020 compared to the same period in the prior year.  The increase was primarily driven by the decline in revenue from lower test volumes during the period, attributable to the impact of COVID-19 as lower revenues were generated to cover fixed costs of performing the tests. The cost of pharmaceutical and clinical services as a percentage of revenue decreased from 59.4% to 45.3% during the three months ended September 30, 2020 compared to the same period in the prior year due to the sale of the Clinic in February 2020.
23


Research and Development Expenses
Three months ended September 30,
(In millions)20202019Change
R&D expense$17.6 $21.3 $(3.7)
R&D expense as a % of sales12.1 %11.4 % 
Research and development expense for the three months ended September 30, 2020 decreased compared to the same period in the prior year primarily due to decreased personnel expenses from a decrease in headcount and decreased technology related expenses from synergies between our labs located in Salt Lake City and in San Francisco.
Change in the Fair Value of Contingent Consideration
Three months ended September 30,
(In millions)20202019Change
Change in the fair value of contingent consideration$(1.1)$0.7 $(1.8)
Change in the fair value of contingent consideration as a % of sales(0.8)%0.4  
The fair value of contingent consideration for the three months ended September 30, 2020 decreased compared to the same period in the prior year due to changes in timing of expected cash payments associated with the contingent consideration related to the Sividon acquisition.  
Selling, General and Administrative Expenses
Three months ended September 30,
(In millions)20202019Change
SG&A expense$124.1 $135.5 $(11.4)
SG&A expense as a % of sales85.5 %72.7 %
Selling, general and administrative expense decreased for the three months ended September 30, 2020 compared to the same period in the prior year primarily due to the Company implementing cost saving measures due to the decline in testing volumes as a result of the impacts of COVID-19 and due to a decline in expense from the sale of the Clinic in February 2020. The cost savings measures implemented by the Company have been partially offset by increased legal expenses and expenses related to our leadership transition in the current six-month transition period ending December 31, 2020.
Other Expense, net
Three months ended September 30,
(In millions)20202019Change
Other expense, net$(4.1)$(1.4)$(2.7)
Other expense, net increased for the three months ended September 30, 2020 compared to the same period in the prior year, due to increased foreign exchange losses and to decreased interest income.
Income Tax Benefit
Three months ended September 30,
(In millions)20202019Change
Income tax benefit$(28.5)$(1.7)$(26.8)
Effective tax rate65.2 %7.6 % 
Our tax rate is the product of a blended U.S. federal effective rate of 21% and a blended state income tax rate of approximately 3%. Certain significant or unusual items are separately recognized during the period in which they occur and can be a source of variability in the effective tax rates from period to period.

24


Income tax benefit for the three months ended September 30, 2020 was $28.5, and our effective tax rate was 65.2%.  The increase in the effective rate for the three months ended September 30, 2020 as compared to the same period in the prior year is primarily due to carrying back net operating losses due to the CARES Act.
Liquidity and Capital Resources
We believe that our existing capital resources and the cash to be generated from future sales, taking into consideration the expected continuing impacts of COVID-19 on our operations, will be sufficient to meet our projected operating requirements and repay the outstanding Amended Facility, which matures on July 31, 2023 and which has no scheduled principal payments prior to that date. Our available capital resources, however, may be consumed more rapidly than currently expected, and we may need or want to raise additional financing. We may not be able to secure such financing in a timely manner or on favorable terms, if at all. We are subject to financial covenants as part of our outstanding Amended Facility. Based on the continued uncertainty regarding the impact of COVID-19 on our future operations, it is possible that we could be in violation of certain financial covenants contained in the Amended Facility within the Amendment Period, which runs through June 30, 2021. We may seek waivers or amendments from our lenders in order to avoid a future potential covenant violation, in addition to taking other potential actions. If we were unable to comply with the covenants in the future, that could result in an increase in the rate of interest and limits on our ability to incur certain additional indebtedness and could potentially cause the loan repayment to be accelerated. Without additional funds, we may be forced to delay, scale back or eliminate some of our sales and marketing efforts, research and development activities, or other operations and potentially delay development of our diagnostic tests in an effort to provide sufficient funds to continue our operations. If any of these events occurs, our ability to achieve our development and commercialization goals could be adversely affected.
Additionally, the COVID-19 pandemic and resulting global disruptions have caused significant volatility in financial markets. This disruption can contribute to potential defaults in our accounts receivable, affect asset valuations resulting in impairment charges, and affect the availability of lease and financing credit as well as other segments of the credit markets. We utilize a range of financing methods to fund our operations and capital expenditures and expect to continue to maintain financing flexibility in the current market conditions. However, due to the continuing rapidly evolving global situation, it is not possible to predict whether unanticipated consequences of the pandemic are reasonably likely to materially affect our liquidity and capital resources in the future.
Our capital deployment strategy focuses on use of resources in the key areas of research and development, acquisitions, debt repayment, and the repurchase of our common stock.  We believe that investing organically through research and development or acquisitively to support business strategy provides the best return on invested capital.
The following table represents the balances of cash, cash equivalents and marketable investment securities: 
(In millions)September 30, 2020June 30, 2020Change
Cash and cash equivalents$118.3 $163.7 $(45.4)
Marketable investment securities42.1 54.1 (12.0)
Long-term marketable investment securities30.2 37.0 (6.8)
Cash, cash equivalents and marketable investment securities$190.6 $254.8 $(64.2)
The decrease in cash, cash equivalents, and marketable investment securities was primarily driven by $59.3 in cash used by operations and the use of $3.8 for the proceeds from the issuance of common stock, net of shares exchanged for withholding tax, offset by $18.6 in proceeds from maturities of marketable investments.
25


The following table represents the condensed consolidated cash flow statement:
Three months ended September 30,
(In millions)20202019Change
Cash flows from operating activities$(59.3)$15.8 $(75.1)
Cash flows from investing activities17.1 (7.1)24.2 
Cash flows from financing activities(3.9)(12.3)8.4 
Effect of foreign exchange rates on cash and cash equivalents0.7 0.3 0.4 
Net decrease in cash and cash equivalents(45.4)(3.3)(42.1)
Cash and cash equivalents at the beginning of the period163.7 93.2 70.5 
Cash and cash equivalents at the end of the period$118.3 $89.9 $28.4 
Cash Flows from Operating Activities
The decrease in cash flows from operating activities for the three months ended September 30, 2020, compared to the same period in the prior year, was primarily due to the $107.9 change in the balance of prepaid taxes and the $17.0 change in the balance of trade accounts receivable, offset by an increase in the unrecognized tax benefit adjustment of $13.2 and an increase in the deferred income tax adjustment of $48.4.
Cash Flows from Investing Activities
For the three months ended September 30, 2020, compared to the same period in the prior year, the change in cash flows from investing activities was driven primarily by the purchase of approximately $23.1 of marketable securities during the same period in the prior year that did not occur during the three months ended September 30, 2020.
Cash Flows from Financing Activities
For the three months ended September 30, 2020, compared to the same period in the prior year, the decrease in cash flows from financing activities was driven primarily by the use of $8.6 in cash for repayment of the credit facility during the same period in the prior year that did not occur during the three months ended September 30, 2020.
Effects of Inflation
We do not believe that inflation has had a material impact on our business, sales, or operating results during the periods presented.
Share Repurchase Program
Our Board of Directors has previously authorized us to repurchase up to $200.0 of our outstanding common stock. We may repurchase our common stock from time to time or on an accelerated basis through open market transactions or privately negotiated transactions as determined by our management. The amount and timing of stock repurchases under the program will depend on business and market conditions, stock price, trading restrictions, acquisition activity and other factors.  As of September 30, 2020, we are authorized to repurchase up to $110.7 under our current share repurchase authorization.  See also “Part II, Item 2. Unregistered Sales of Equity Securities and Use of Proceeds – Issuer Purchases of Equity Securities”.
Critical Accounting Policies
Critical accounting policies are those policies which are both important to the presentation of a company’s financial condition and results and require management’s most difficult, subjective or complex judgments, often as a result of the need to make estimates about the effect of matters that are inherently uncertain.  No significant changes to our accounting policies took place during the period. For a further discussion of our critical accounting policies, see our Annual Report on Form 10-K for the fiscal year ended June 30, 2020.
26


Item 3.    Quantitative and Qualitative Disclosures About Market Risk

There have been no material changes in our market risk during the three months ended September 30, 20192020 compared to the disclosures in Part II, Item 7A of our Annual Report on Form 10-K for the fiscal year ended June 30, 2019,2020, which is incorporated by reference herein.

Item 4.    Controls and Procedures

Evaluation of Disclosure Controls and Procedures.  

Our principal executive officer and principal financial officer, after evaluating the effectiveness of our disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) as of the end of the period covered by this Quarterly Report on Form 10-Q, have concluded that, based on such evaluation, our disclosure controls and procedures were effective to ensure that information required to be disclosed by us in the reports that we file or submit under the Exchange Act is recorded, processed, summarized and communicated to our management, including our principal executive and principal financial officers, or persons performing similar functions, as appropriate, to allow timely decisions regarding required disclosure.

In designing and evaluating our disclosure controls and procedures, our management recognized that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired control objectives, and our management necessarily is required to apply its judgment in evaluating the cost-benefit relationship of possible controls and procedures.

Changes in Internal Controls  

The Company is in the midst of a multi-year transformation project to achieve better analytics and process efficiencies through the use of Oracle Fusion Cloud Services System. During the three monthsquarter ended September 30, 2019, we2020, the Company completed the implementation of certain modules used in the financial statement close process and management reporting. Additional phases will continue to be implemented changes to our processes in response toover the adoptioncoming year. Emphasis has been on the maintenance of Accounting Standards Update No. 2016-02 “Lease (Topic 842)” that became effective July 1, 2019. Theinternal controls and assessment of the design and operating effectiveness of these changes will be evaluated as partkey control activities throughout development and deployment of our annual assessment of the effectiveness of internal controls over financial reporting.

each phase.

Other than as described above, there were no changes in our internal control over financial reporting that occurred during the quarterthree months ended September 30, 20192020 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

28

27


PART II - Other Information

Item 1.    Legal Proceedings

Investigations of the Department of Health and Human Services, Office of Inspector General

In July

Purported Securities Class Action Claims

On September 27, 2019, we resolved thea purported class action complaint was filed by a qui tam relator in October 2017 in the United States District Court for the District of South Carolina.  The complaint was the basis of the Office of Inspector General (OIG) subpoena dated February 2018 regarding Medicare billing practices relating to the Company’s hereditary cancer testing from 2014 to 2018.  After a 17-month investigation, the Department of Justice declined to intervene in the case.  The Company believes it demonstrated that the key allegations made in the complaint were false.  In order to avoid a lengthy and distracting litigation with the qui tam relator, we entered into a settlement agreement on July 18, 2019 under which we would pay $9.1 million to the qui tam relator in order to settle the matter. The settlement was approved on October 23, 2019 andUtah, against the Company, paid the settlement amount of $9.1 on October 29, 2019. The Company denies any wrongdoing and does not anticipate any material change in billing practices.

In June 2016, our wholly-owned subsidiary, Crescendo Bioscience, Inc. (“CBI”), received a subpoena from the Office of Inspector General of the Department of Health and Human Services requesting that CBI produce documents relating to entities that received payment from CBI for the collection and processing of blood specimens for testing, including a named unrelated company, healthcare providers and other third party entities.  The Office of Inspector General subsequently requested additional documentation in December 2017.  CBI has provided to the Office of Inspector General the documents requested and continues to cooperate with any follow-up requests.  We are unable to predict what action, if any, might be taken in the future by the Office of Inspector General or any other regulatory authority as a result of the matters related to this investigation. No claims have been made against CBI.

Purported Securities Class Action Claims

On September 27, 2019, Ethan Silverman, individually and on behalf of all others similarly situated, filed a purported class action complaint in the United States District Court, District of Utah, No. 2:19-cv-00707-PMW (“Silverman Action”), against us, ourits former President and Chief Executive Officer, Mark C. Capone, and ourits Executive Vice President and Chief Financial Officer, R. Bryan Riggsbee (collectively(“Defendants”). On February 21, 2020, the “Defendants”).plaintiff filed an amended class action complaint, which added the Company’s Executive Vice President of Clinical Development, Bryan M. Dechairo, as an additional Defendant. This action, captioned In re Myriad Genetics, Inc. Securities Litigation (No. 2:19-cv-00707-DBB), is premised upon allegations that the Defendants made false and misleading statements regarding our business, operations, and acquisitions. The lead plaintiff seeks certification as the purported class representative and the payment of damages allegedly sustained by plaintiffit and the purported class by reason of the allegations set forth in the amended complaint, plus interest, and legal and other costs and fees. The Company intends to vigorously defend against this action. 

Due to the nature of this matter and inherent uncertainties, it is not possible to provide an evaluation of the likelihood of an unfavorable outcome or an estimate of the amount or range of potential loss, if any.

Other Legal Proceedings


On August 24, 2018, our wholly-owned subsidiary, Assurex Health, Inc. ("Assurex") was served with an Amended Complaint which had been filed in the Circuit Court of Cook County, Illinois, County Department, Law Division, Civil Action No. 2018 L 004972, by Pipe Trades Services MN Welfare Plan ("Pipe Trades"), as a qui tam relator, on behalf of the State of Illinois, Pipe Trades, and all others similarly situated, purportedly arising from Assurex's alleged violations of the Illinois Insurance Claims Fraud Prevention Act and other causes of action. Pipe Trades seeks certification of a putative class, certification as the purported class representative, and the payment of treble damages allegedly sustained by Pipe Trades and the purported class by reason of the allegations set forth in the amended complaint, plus statutory damages and penalties, plus interest, and legal and other costs and fees. The State of Illinois and Cook County, Illinois, have declined to intervene in the matter. On September 11, 2019, plaintiffs filed a second amended complaint, and on October 10, 2019, Assurex filed a Motion to Dismiss Plaintiff’s Second Amended Complaint for Lack of Personal Jurisdiction and Standing, requesting that the second amended complaint be dismissed in its entirety, with prejudice, for lack of personal jurisdiction and standing. We intendOn July 20, 2020, this motion was denied. The Company’s motion filed on August 12, 2020, for interlocutory appeal of the denial of the motion to dismiss, was denied in a hearing on October 30, 2020. The Company intends to continue to vigorously defend against this action. Due to the nature of this matter and inherent uncertainties, it is not possible to provide an evaluation of the likelihood of an unfavorable outcome andor an estimate of the amount or range of potential loss, if anyany.
.  

Qui Tam Lawsuit

In June 2016, our wholly-owned subsidiary, Crescendo Bioscience, Inc. (“CBI”), received a subpoena from the Office of Inspector General of the Department of Health and Human Services requesting that CBI produce documents relating to entities that received payment from CBI for the collection and processing of blood specimens for testing, including a named unrelated company, healthcare providers and other third party entities. The Office of Inspector General subsequently requested additional documentation in December 2017. CBI provided to the Office of Inspector General the documents requested. On January 30, 2020, the United States District Court for the Northern District of California unsealed a qui tam complaint, filed on April 16, 2016 against CBI and the Company, alleging violations of the Federal and California False Claims Acts and the California Insurance Fraud Prevention Act. On January 22, 2020, after a multi-year investigation into CBI’s and the Company’s alleged conduct, the United States declined to intervene. On January 27, 2020, the State of California likewise filed its notice of declination. The Company was not aware of the complaint until after it was unsealed. On May 23, 2020, the court denied CBI and the Company’s motion to dismiss. The Company intends to continue to vigorously defend against this action. Due to the nature of this matter and inherent uncertainties, it is not possible to provide an evaluation of the likelihood of an unfavorable outcome or an estimate of the amount or range of potential loss, if any.
Other than as set forth above, we are not a party to any legal proceedings that we believe will have a material impact on our business, financial position or results of operations.


28


Item 1A.    Risk Factors

There have been no material changes to

The following risk factor disclosure should be read in conjunction with the risk factors includeddescribed in ourthe Annual Report on Form 10-K for the fiscal year ended June 30, 2019.

29


2020.
We may be adversely impacted if we are unable to successfully implement new systems or unable to adapt systems to our change in fiscal year-end.

Information technology systems are an important part of our business operations. We are in the midst of a multi-year transformation project to achieve better analytics and process efficiencies through the use of Oracle Fusion Cloud Services System ("Oracle Fusion"). This project is expected to improve the efficiency and effectiveness of certain financial and business transaction processes and the underlying systems environment. During the quarter ended September 30, 2020, we completed the implementation of certain modules used in the financial statement close process and management reporting. Additional integrations are expected to take place over the next year. An implementation of this nature is a major undertaking from a financial, management and personnel perspective. The implementation of Oracle Fusion may prove to be more difficult, costly, or time consuming than expected, and there can be no assurance that this system will be beneficial to the extent anticipated.

In addition, we have announced a change in our fiscal year end from a fiscal year ending on the last day of June of each year to a calendar fiscal year ending on the last day of December each year, effective January 1, 2021, which will require certain modifications to our systems used for accounting and management reporting. If the systems are not appropriately configured for the change in fiscal year-end it could have a material adverse effect on our results of operations and financial condition.

We are subject to debt covenants that impose operating and financial restrictions on us and if we are not able to comply with them, it could have a material adverse impact on our operations and liquidity.

Covenants in the Amended Facility impose operating and financial restrictions on us. These restrictions may prohibit or place limitations on, among other things, our ability to incur additional indebtedness, create certain types of liens, and complete mergers, consolidations, or change in control transactions. Under the Amended Facility, a change in control of the Company, which means that a shareholder or a group of shareholders is or becomes the beneficial owner, directly or indirectly, of more than 35% of the total voting power of the voting stock of the Company, would require mandatory prepayment of the outstanding debt. The Amended Facility may also prohibit or place limitations on our ability to sell assets, pay dividends or provide other distributions to shareholders. These restrictions could also limit our ability to take advantage of business opportunities.

We must maintain specified leverage and interest ratios measured as of the end of each applicable quarter as financial covenants in the Amended Facility. The Amended Facility, through Amendment No. 2 entered into on May 1, 2020, modified compliance with the leverage covenant and the interest coverage ratio covenant, which were waived through March 31, 2021, and added a minimum EBITDA covenant for the quarters ending December 31, 2020 and March 31, 2021. Based on the continued uncertainty regarding the impact of COVID-19 on our future operations, it is possible that we could be in violation of certain financial covenants contained in the Amended Facility within the modification period, which runs through June 30, 2021.

If we are unable to comply with the covenants and ratio in the Amended Facility, we may be in default under the agreement. A default would result in an increase in the rate of interest and limits on our ability to incur certain additional indebtedness and it could potentially cause the loan repayment to be accelerated, any of which could have a material adverse impact on our operations and liquidity.

Item 2.    Unregistered Sales of Equity Securities and Use of Proceeds.

Issuer Purchases of Equity Securities

In June 2016, we announced that our

Our Board of Directors hadhas previously authorized us to repurchase an additionalup to $200.0 million of our outstanding common stock, increasing the cumulative shareof which $110.7 million is still available to repurchase authorization since we first authorized the program in May 2010 to $1.4 billion. In connection with our most recent stock repurchase authorization, we have beenas of September 30, 2020. We are authorized to complete the repurchase through open market transactions or through an accelerated share repurchase program, in each case to be executed at management’s discretion based on business and market conditions, stock price, trading restrictions, acquisition activity and other factors. As of the date of this report, the Company has used $50.0 million to repurchase shares of the Company’s stock as part of an accelerated share repurchase under our most recent stock repurchase program. The repurchase program may be suspended or discontinued at any time without prior notice. The transactions effectuated to date occurred in open market purchases.

The details of the activitypurchases and pursuant to a trading plan under Rule 10b5-1.

No stock repurchases were made under our stock repurchase programsprogram during the three months ended September 30, 2019, are as follows:

2020.

(a)

(b)

(c)

(d)

Total Number of

Approximate Dollar

Shares Purchased as

Value of Shares that

Part of Publicly

May Yet Be

Total Number of

Average Price Paid

Announced Plans or

Purchased Under the

Period

Shares Purchased

per Share

Programs

Plans or Programs

July 1, 2019 to July 31, 2019

$

110.7

August 1, 2019 to August 31, 2019

$

110.7

September 1, 2019 to September 31, 2019

$

110.7

Total

110.7


29


Item 3.    Defaults Upon Senior Securities.

None.

Item 4.    Mine Safety Disclosures.

None.

Item 5.    Other Information.

None.

Item 6.    Exhibits.

31.1

10.1
10.2*
10.3
10.4
10.5
10.6
31.1

31.2

31.2

32.1

32.1

101.INS

101.INSInline XBRL Instance Document - the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document.

101.SCH

101.SCHInline XBRL Taxonomy Extension Schema Document

101.CAL

Inline XBRL Taxonomy Extension Calculation Linkbase Document

101.DEF

101.DEFInline XBRL Taxonomy Extension Definition Linkbase Document

101.LAB

101.LABInline XBRL Taxonomy Extension Label Linkbase Document

101.PRE

101.PREInline XBRL Taxonomy Extension Presentation Linkbase Document

104

104The cover page from the Company’sCompany's Quarterly Report on Form 10-Q for the quarter ended September 30, 2019,2020, has been formatted in Inline XBRL.

* The appendix to this exhibit has been omitted pursuant to Item 601(a)(5) of Regulation S-K. A copy of the omitted appendix will be furnished to the SEC upon request.



30



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.

MYRIAD GENETICS, INC.

Date: November 5, 2019

9, 2020

By:

By:

/s/ Mark C. Capone

Paul J. Diaz

Mark C. Capone

Paul J. Diaz

President and Chief Executive Officer

(Principal executive officer)

Date: November 5, 2019

9, 2020

By:

By:

/s/ R. Bryan Riggsbee

R. Bryan Riggsbee

Executive Vice President, Chief Financial Officer

(Principal financial and chief accounting officer)


31