Bruce C. Cozadd
Kathy. everyone, and for you, afternoon, Good joining Thank us. thank you
MAA compared fronts. XXXX, quarter the on in same X% Matt and for over X% and to in our review During both XXXX. for months, clinical expected financial in turn submitted the or results Vyxeos the Technology year-to-date million $XXX more to XXXX, launched Authorization delivered and to our Marketing CMS's guidance. senior for before on growth Payment significant approval and the submitted and the progress legal, area, and detailed made few revolver In financial Canada, updates update our a therapeutic periods Defitelio We Xyrem notes quarter multiple the EU, sleep Vyxeos the third commercial, activities announced outstanding key of After in we've call for repay key us received balance. sales the year-end, application exchangeable and and events some highlighting regulatory in Application to U.S. ImmunoGen, past I'll fully issued providing agreement the Add-on due Vyxeos New with option fiscal collaboration in year allowing
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during This quarter, continued rates, we year-to-date. experienced and grow reimbursement to steadily the enrollments quarter high consistent payer and approval patient
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is an we've narcolepsy can of fills growth we new that We from new enrollments that generate consecutive accurate awareness making over difference, second patients time give diagnosis. improvements earlier time a confidence observed patient to investments narcolepsy are we the in rates XXXX. insurance helping obtain us in patient made believe on new in of improvements volume and first continue narcolepsy This have through the We seen The patients. recent quarterly years. diagnosis, positive have narcolepsy data first review our diagnosis in the based quarter claims growth
dosing related excessive daytime for our sleepiness. oxybate supplemental support other plans patients for Drug sNDA with in submit of use to planned and our cataplexy The Xyrem the amounts smaller narcolepsy dispenser Xyrem programs, drug pediatric sNDA to includes or a pediatric request help the response and In highlight Application for with order the in with New plan pediatric which written provide data starting dosing the sNDA now I'll dosing to Next, R&D dispenser to of submission, new the mid-XXXX. accurate new we ensure will of patients.
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and litigation brief against filed for Xyrem, legal Amneal, a Turning companies that of four Par, continues a version property the ANDAs intellectual update of patent Watson and on generic Lupin. have Xyrem, to
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had September a pre-NDA planned excessive OSA narcolepsy. and are in FDA NDA meeting in JZP-XXX, our year-end for for on the with and sleepiness treatment to Turning we submission of track
the unmet about with for to real wake-promoting long-term a opportunities bring need. agent where FDA We patients forward the are there working JZP-XXX is novel look and this to to excited
process take that DEA year approximately expect followed will review the We scheduling. by FDA one
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achieve our key initiatives drive are to three which U.S. continue We designed launch objectives. to
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make NCCN the that in will recommendations term. hopeful are We near
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