listening today. Allison. Thanks, morning, everybody Good
Biopharma, support a the compelling all first as we value Let commercially are call me Biopharma, proposition. as Strongbridge company Xeris Xeris shareholders one Xeris a focused overwhelming Biopharma of our result operating as with to approval and both biopharmaceutical very of by now Pharmaceutical you start of and welcoming
the to profile talking spend a of the couple I’d company. about minutes new context, like For
a have very diversified base. revenue We
large current over that potential Our established us revenue give in years. strong the addressable markets and growth growing presence double-digit the several next Gvoke assets, already revenue has commercial Keveyis to generate a rapidly base
the With rapid XXXX leveraging the commercial by infrastructure. of Recorlev approved if our in additional for FDA, quarter the experienced launch first of potential endocrinology-focused opportunity
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a We also have robust pipeline.
Xeris for and under relatively In addition small a to FDA and of the review programs. young extensive which is pipeline filed by Recorlev, development company, has an
commercial new We and current marketed and have into developments important new support the well forward of using in to long-term extend as product our as formulation indications products bringing platforms technology opportunity uses, products success.
financial very are we strong also Importantly, a position. in
commercial functions a immediate This general We XXXX public an XXXX pre-tax quarter we from notably have we investments, infrastructure team. the for of will and $XXX other most of year company the resulting realize in savings, end forecasted cash approximately and and million cost is cost, by end the including cash synergies acquisition within equivalents million Strongbridge have reporting avoidance $XX from us. including management experienced administrative cost unique
just third acquisition report completed are quarter into was financials, week Strongbridge We one required to standalone yet the of Xeris QX.
only available XXXX, approvals the of results room a well FDA with for compared performance XXXX I say some very We Kit, announced XX am year impact combined subcutaneous period as collaboration end. an months. as up Syringe – the second UK the pro our technology, on accurately, of XeriJect XX% in of HypoPen Merck $XX position forma partnership highlights well enrollment shelf-life that for as guidance and near-term more had net debt of The Keveyis in before and up With Gvoke will with be had to-date the on of potential is levothyroxine once-weekly a injection of as quarter healthy our Steve growth will forma quarter as So, Gvoke the Prefilled temperature additional and once we and the we into happy months the pro on a positive of later. acquisition. XX% bit at from Xeris of that, and interest Gvoke metrics. they key achievement has acquisition. full track coming extension completed our the which quarter-over-quarter. into an which X is to to million million our our The our of will study, Gvoke evaluate Strongbridge Xmg quarter of facility, milestones XX% Phase provide cash our to quarter, company stated. $XX to a that $XX the integration million, $XX.X EU end of using $XX allowing sNDA Steve and include, QX, go will cash, cash QX Keveyis XXXX third detail million the little Pharma sales Other importantly, with plus respectively. the of for initiation I That launch details Ogluo extension of XX versus and of go with more close was million $XX.X a Tetris to the on the are in year million revenue very into again, completed the of the strong and the second combined the
start the into deeper with Gvoke. little a I’ll specifics, Going
We of owe quarter-over-quarter to a We continue prescription in that Gvoke demand few growth. see terms market factors. for and strong to
have believe with the product. we we – product, best Our
the prescription growth total The and growth commercially? second a is XXXX. XX,XXX up was we over with excellent first coverage saw are Our taking up is uptick to end market in for the by $XX this for earlier the continues market of growth of footprint from net XX% to Gvoke the X% XX% XX% increasingly in market effort; our prescriptions in glucagon year. prescribers; insulin and XX% an with sales as impactful up million are quarter, all to XX% increased sales of – supported extended from from QX Our up which time at payer the commercial which QX from is grew message, sales improving up were to unrestricted. patients that Gvoke’s our offices; outpace October. the the coverage and the What of field terms significant Gvoke’s TRxs physician QX glucagon from - and of QX. Gvoke insight XX% end up access add topping to we continued to share, beginning QX XX% our all
from that to maintain slightly tend perhaps basis. As fourth quarter you we comfortable in Sitting an over today, or on based am quarter. annual glucagon the on even market increase quarter can quarter third I know, saying recent here fourth third the prescriptions decrease prescriptions prescriptions, the
to on move Keveyis. Let’s
paralysis first approved for X,XXX PPP, diagnosed only We periodic primary The condition. with estimate a or FDA to and PPP. severe therapy people each year X,XXX
established quarter-over-quarter growth expertise driven revenue disease year-over-year. has Our commercial and and of Keveyis rare experience
revenue of revenue XXXX $XX the exceeding of increase last sales of million given $XX million. XX% million XXXX net of the quarter Year-to-date to QX third we impressive XXXX. year. historical over million of over that The will increase a be range represents million full results, And in XX% believe $XX.X to $XX an million guidance is year $XX.X $XX
briefly pipeline, talk well. me start I’ll about Let Recorlev. our as with
fit treated syndrome penetration. the and therapy, an the are drive we’ve X,XXX the we to controlled. treated acquisition U.S. opportunity early give an of Strongbridge syndrome the the Cushing’s are a is in as tremendous with approximately, like As market diagnosed, for XX,XXX I’d articulated, part Cushing’s commercial existing X,XXX ketoconazole. some whom patients value with will of on Recorlev of estimated opportunity, infrastructure, background Many not which of the with unapproved There prescription of including Gvoke’s well. patients which these generics, are being well patients are estimated believe
penetration market endocrinology have significant reimbursement established Gvoke, offices in gaining dominated dedicated plus approved by XX patient liaisons, with by $X we science of and prescribing date today this believe billion support January Recorlev? market. are The under generics. review we PDUFA overlap of been reps, products branded drive CS our medical a with on share is in Where and X, However, with capitalize experience, addressable could what currently NDA field relationships with a With the Recorlev our FDA be once can XXXX. we services, the
mentioned, in injection stage And the I levothyroxine of full study mode first launch. We potential pharmacokinetics, earlier programs, subcutaneous drugs treatment for our successfully and subcutaneous the in anticipation we of our the dosed one as in tolerability of Phase initiated pre-commercialization once-weekly and dosing terms potential formulation all quarter are U.S., X in the in most safety a of for of participants in prescribed to levothyroxine, a evaluate preparation for weekly and a novel hypothyroidism. for the our
We achieve can dosing. will from in that first X once-weekly indication not XXXX, we us Phase expect results which the give the of whether half of, study or an
the the ready-to-use agreement we in first in quarter In of ultra-high For use suspension-based for sub with Exercise-induced Exercise-induced addressing Hypoglycemia, purpose the our for undisclosed engineering collaboration technology, to generate monoclonal of and clearance, upon formulations. license announced Hypoglycemia formulation Merck, submit of October, antibodies will data with more we XeriJect, an XXXX. option with an concentration, management IND the XXXX, clinical
are we on excited quite working expect, Merck this to would be with you project. As closely
As some understand of we’d you I my some to stated our can guidance provide important to the earlier value metrics remarks, like better performance. in
of million to $XX year sales, is full we million in million the expect Keveyis. $XX XXXX, $XX which to For net million $XX from
year an sales to we million. we also our XXXX not is of cash $XXX after full basis. year deal-related impressive fourth this expect for and products We combined quarter one-time to When commercial early of million individual expenses. and position $XX an product expect with be full in net year report on March, providing the And approximately end
to Now Steve performance. will over the our to I financial call review details turn of