Thank to welcome, you, and everyone, today's call.
with achievements our to by be you quarter, highlighted We today in launch third are remarkable of Ohtuvayre. the pleased share the extremely to
Hahn, Chief Officer; our Chris today Chief our Rheault, Officer; me Kathy With Commercial Officer; Chief our Mark Medical our Martin, Rickard, Development are Officer. Tara Chief Dr. Financial Dr. and
The and third for of exceptional treatment by marked our maintenance the of Pharma, COPD U.S. Verona launch progress development the programs. Ohtuvayre on clinical quarter continued for was
benefits patients. broad product First, outstanding grounded provides its Ohtuvayre, the $X.X launch million COPD were sales After quarter. COPD Ohtuvayre compelling indication third which let's in to just X and net is of the review weeks, the for
continues with sales net exceeding escalate, third for to We are as quarter. Ohtuvayre demand excited for October the
Ohtuvayre. of Ohtuvayre, than Through metrics. more have end more HCPs filled, prescriptions launch October, Ohtuvayre fully unique XX X,XXX been key some X,XXX the review let's prescribing than weeks only Now after launching with
HCPs. Ohtuvayre to on Our launch highest the promoting efforts prescribing continue focus XX,XXX to
prescribed HCPs X,XXX Tier weeks, XX of approximately In have Ohtuvayre. X XX% our
XXX treatment HCPs reminder, write per on As month. X Tier COPD maintenance average prescriptions a
prescribing continue to in more patients to practice. their Ohtuvayre, an also increased prescribes see their We they HCP once that
and this We impressed by the prescribers early breadth of depth in the prescriptions are and launch.
and approximately patients, patient of research our significant This therapy. market XX% patient are broad dual and background a on all broad COPD with utilization the including Ohtuvayre to single, across Importantly, consistent range the population. across triple across continues prescribing COPD HCPs is types need unmet highlight
from impact deliver regardless health severity is and COPD, about of Ohtuvayre meaningful and early patients is a feedback the care extremely the potential against to background all disease of and Initial both refill supported by encouraging data. therapy, providers
more HCPs to month. commercial Our and Tier continue of Through increase of X our promotion. digital through weeks engage or X XX over Tier reached activities the in-person than month to launch, we first XX% have HCPs
well continue XXX Ohtuvayre Presentations ENHANCE Our to unmet speaker new need by accelerate, COPD with as have ERS analysis and data. from efficacy end and Ohtuvayre at evaluating as expect real-world HCPs the and subgroup CHEST in XXXX.
We on claims COPD. we highlighted conferences studies the and III care safety in health utilization approximately presented the based the to Phase programs of resource from trial impact COPD-related of ENHANCE analysis programs pooled in the on recently completed
for booths approximately At at HCPs. of in from our high interest CHEST, X,XXX Ohtuvayre interacted commercial and highlighting Ohtuvayre, our HCPs with team the medical level
While start the to it's the launch, still very we commercialization of encouraged Ohtuvayre. are early by the U.S. extremely in strong
nonsteroidal the COPD anti-inflammatory treatment redefine paradigm. first can bronchodilation confident Ohtuvayre is the we provide to inhaled both are it COPD and and that treatment effects,
a centers be the J-Code We for Ohtuvayre, approved which and XXXX. product-specific Medicaid in Medicare effective services permanent recently are for also pleased to report will January
glycopyrrolate, treatment with standard via quarter. during the Ohtuvayre the LAMA, our II Phase enrollment nebulizer. a fixed-dose delivered third clinical a a of initiated dose-ranging II Alongside for supporting programs ensifentrine launch, new successful a Phase maintenance began formulation September, jet In in we trial and X COPD combination
and X-week of the crossover is in trial randomized, glycopyrrolate via dose-ranging approximately XX function, delivered placebo-controlled, COPD. with safety double-blind, pharmacokinetic subjects to profile the lung The a trial nebulizer assess
range, of identification combination of fixed assessing trial be II ensifentrine dose an and the dose a conducted. Phase appropriate glycopyrrolate Following glycopyrrolate will
Also nebulized in placebo-controlled fibrosis randomized enroll non-cystic a in parallel with assess trial group trial ensifentrine enrollment Phase bronchiectasis. recent of The in pulmonary to patients subjects II began September, will history exacerbations. XXX with double-blind, the
least the and The ensure driven, exacerbation trial events pulmonary the will robust quality are on is required until event ensifentrine the for number the daily symptoms assess life. risk with effect subjects X-milligram of treated and powering, To and exacerbations, trial of XX twice at weeks of observed. rate all of
announced in update Pharma partner China, expects evaluating next turning Finally, in clinical maintenance for we providing pivotal development from for it to in enrollment year. pivotal to ensifentrine III forward Pharma, to our in completed COPD Nuance Phase the results trial III Nuance provide Phase trial an treatment ensifentrine its the our Greater China. look and XXXX, has of strategy. global clinical
quarter. now will review for over third I turn Mark the results call the to our financial to