everyone us our thanks results. taking and operating morning, you, year join full and for achievements we XXXX. time discuss Good significant another reported with in to strong the Thank of Supernus Peter. results XXXX fourth year quarter as
continued The achievement on XR. execution the is and strong Trokendi commercial first XR Oxtellar
performance. Following the brands us and in total diluted highlight revenues million, $X.XX. growth deliver launches operating enabled a to in heavily the market solid of that double-digit sixth a intense in is growth to of total robust $XXX earnings was growth for prescriptions XXXX, of from XXXX in three delivered important market. the that total two achieved year in in company a delivered reaching now compared solid by grew XX% new to growth financial year prescriptions $XXX record We promoted that are another in saw class prescription in that million on our their This It new with competition earnings in share XXXX per XX% migraine drugs. year
at in of high around its share For increased million Trokendi of market total at held grown steady XX.X XXXX market market the prescriptions while topiramate Trokendi share X.XX% XX% despite topiramate XR, end prescriptions. up XX% XXXX. has all-time an by XR year reaching competition, increased the
of XX% another increased level For Oxtellar to suboptimal year compared of XR, promotion prescriptions for full XXXX despite year the competition.
significant to include Oxtellar label long-term growth the for in for we with of to launched in seizures of represent label is expansion monotherapy seizures monotherapy and Oxtellar XXXX opportunity this FDA expanded achievement include The the its Oxtellar we monotherapy XR. XR. quarter, for in Early partial second can partial XR believe major approval that a
generating studied extensively market efficacy. partial X.X market than a year, significant a efficacy epilepsy data safety market strong drug eight at a studies XX and million its of oxcarbazepine in prescriptions has estimated prove monotherapy has is monotherapy. oxcarbazepine The its wealth prescriptions million anticonvulsant, proving that been the much larger an general about The with As data year. in of monotherapy seizure approximately a
achievement Phase X successful three the results trials novel our line completion these The we from in candidate with The statistical trials third its SPN-XXX. onset across in trial point product significance. major and XXXX efficacy, primary announced product of December a top is lead ADHD safety with fast end Each action good profile to point a met trials. strong well differentiated all of with a robust pipeline
to for showed aspect important which efficacy strong the an non-stimulant. the sub-scales, that, trials addition the In any inattention very is on hyperactivity and
to trial adolescent the We results disclosing forward are line from by of the March. end final top looking second and
We continue of XXXX file NDA FDA for the for second the product to the half of be second the pending on and half XXXX. launch the in in SPN-XXX of track approval to
patients We adult in to are also a of planning the X this start in program year. half Phase second
profile with clinical for We differentiated remain about late patients our believe potential a what important have well therapeutic we now to as non-stimulant the of one new SPN-XXX products ADHD. de-risked stage enthusiastic and pipeline offer of an
we SPN-XXX an of and remains half patient addition at treatment in ADHD. Enrollment observe with aggression on the of and the a made believe efficacy significant in tolerability is report average encouraging expect patients to nearing year. the we enrollment profile is of higher. achievements, progress on this this novel impulsive treatment to open and which we have good of second Supernus In these the SPN-XXX XX% months program results label completion on XX study in for On label unique novel or SPN-XXX, to in our SPN-XXX. for sign continues extension open study
SPN-XXX of to We FDA launch to the XXXX submit drug approval the pending half for by expect second and the in the an NDA half in second to continue of XXXX.
of XXXX. the for is program of the Regarding half to commence expected SPN-XXX in disorder X treatment Phase second the bipolar
SPN-XXX progress completed opportunity an In adding epilepsy. acquisition addition stage Neurotherapeutics for above the pipeline we our exciting Biscayne on to the severe XXXX programs late pipeline in of
and in neurology represent for strategic side Our with that a activity will psychiatry looking portfolio. XXXX corporate our fit assets continue on the development
Investor programs Finally, will where we be an including over our who an Greg, our you quarter with year will a issued full full on the market hosting our clinical last now assessment New announced we of to call XXXX, SPN-XXX share year detailed fourth in overview provide opportunities. details night, discussion and on as quarter more company and Day associated financial the XX, an results of York we especially in of our fourth April I release and will turn performance. press will