good that to had a and Allison, and we’re morning, for report strong today. us you, XXXX. Thank I’m off a first happy to to start and everyone for quarter we thanks joining good
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quarter from Barry also further first which improvement gross-to-net, remarks. our in Our his in sales discuss an net will benefited
translates that gap who how note there unit IQVIA, into prescriptions that you will of those reported For remains follow a between sales. you and
As the time. will that we have we gap believe indicated past, reporting in narrow over
through with programs, the registered March. in different our remarks. entirely my on I’ll FDA direct Working the discussions offering in a in Deerfield clinical ready-to-use the important MRA Our additional approval in detail position markets two which as and Ogluo more brand -- clearance regulatory an outside February in in three MHRA We cash with by approval rescue million the -- I U.S. glucagon received product for EMEA countries $XX advanced said in we virtually name U.K. EU strengthened April. discuss and later
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it. Deerfield in and detail to discuss initiatives, appreciate success these those will and With Oxford/SVB continue remarks. Barry more commitment to during show his long-term events sincerely we their Xeris
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First, let it the us, talking to I’m as say pandemic. sure we we’d few it everyone with behind to on what and will. me everyone Like preface continued words the would effects about like about a call, of to see like stop COVID-XX I’m this about
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our XX% most result, in customers been face-to-face our our being of the customer -- and As increasingly few some engage sales XX% customers now we’re interactions to In the XX% weeks, have able few person. weeks is a in recent team organization of field than more last seeing approaching face-to-face.
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expected of our previously they EU Turning the select received we have better had cash has Europe in countries, be focusing vaccine mentioned plan countries watching our way markets giving glucagon the U.K., Europe, very than that and better approach And in February for Europe the within Lily’s would securing briefly to strategy EU we announced paying Ogluo had in pricing -- in for given to private for and as much we we commercialization this launch in to select Relative as success only on key Europe changed. believe been the I April, approval and for pricing. Initially, ready-to-use closely. launch, best that -- their respectively.
attractive prove ourselves a are most potential first also $XXX However, still excuse in commercialization at strategy in we’ve to year? of not, European timeframe. pursue since time. country more expect reimbursement broader select in renewed If before in Should me, from will this various Ogluo coordinate the launch our a countries we these stages of that at several. countries, interest of the discussion or is discussions approximately and partners the we or with Not more similar could appears the end fruitful, launch a you we to opportunity us seen we surprisingly, countries vaccine EU U.S.
Let’s move our on pipeline. to
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I drug we forward find of As with can a optimistic history mentioned, approved we reasonable remain safety. these or for both that very an one programs long for of a path
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the an meetings juncture, these of needed of to aspects avenue in that increasingly these At the been we has population. difficult programs this hasn’t can of for fact unique due trials pursue on have but -- as the not we dialogue microdosing on for As become do new. calendar either and programs to mini continue would able any the possible and say that beginning for I taking in-person are basis to it that insulin many pandemic, the of FDA a to XXXX, anticipate
falls co-formulation diabetes. other is pathway control confirm we the improve product that As this quarter, program, first product in including to indications that the the that in -- A for programs, of with our BLA FDA patients and the pramlintide-insulin glycaemic XXX(k) in the
actively X Type to we co-formulation with our and regarding anticipate in on process diabetes and submitted -- third Type from glycaemic we’ve control product. for request as diazepam as clarification a our further our with the a FDA X we’re quarter. Phase about partner two that our to talked meetings broad the the As proposal to patients support programs, X license the for effect license out a mentioned in initiate response for an previously, indication. Based program We previously, other we feedback, out also feedback follow-up received clinical we’ve will seeking for studies explore as
successful well over for Barry year set I briefly. a Before moving are priorities. have We stay turn quarter we manner begun financials, are summarize second quarter and up first we very our the very forward the and and in critical a to positive me let the believe focused we on --we had for
Gvoke development growth our subsides, diabetes promotional steadily momentum opening continuing license demand grow to insulin select drive to for patients Gvoke First, with as pipeline all pandemic the continuing for and commensurate taking especially footprint Gvoke, of with enterprise. marketplace, fund of XeriSol development in our and an our a commercialization to quarter, and growth expanding programs aggressively commercial the fourth out to message, either the seeking with and internal for launch ourselves, or the partners, partnerships XeriJect advancing preparing technology the and managing by select in financials of through the in our platform carefully the partner continued countries our external Ogluo to EU
our Barry highlights. financial that, with the me discuss call So to over let turn to