call for this afternoon. Well, the thanks Erik the in the for thanks participants comments,
pipeline specifically programs, clinical As updates which some moving well. all our Kevin on mentioned, along provide five are I’ll
So two programs. with the let's start valbenazine
about long-term that psychiatric commercial and we accepted steady of The team three We and publication neurology. tardive psychiatry of at dyskinesia, College later patient pleased manuscripts and connect extension multiple the the Erik, year up flow including been engagement leaders scientific submitted has with clinical just scientific been sharing a importance. American data upcoming are INGREZZA been stability First very anticipate medical do has from with XXXX. up other more also successful topics of of launch both coming data, group aspects affairs of and is meetings with specific data has in the having which subtype planned heard Psycho-Neuropsychopharmacology this the for analyses, you recently medical our affairs in the including
valbenazine a sufficient in important modeling with study, data design our up GOLD response set to were screen. to is currently that T-Force with granted screen For that of T-Force up study, the from FDA that wrapping data And clinical which with open followed we're us the study. orphan designation patients the the exposure some got study, T-Force we busy we've The Syndrome, very for T-Force is fusion study extension with pleased that label very conjunction was Tourettes. for fusion Tourette recently which pediatric disease team come because able
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and placebo last optimization in new randomization controlled dose see will it placebo. trial our The that II and controlled the six valbenazine placebo controlled a T-Force You period subjects, rate kids being conducted the years And complete data offer late prior patients beginning trial The our for trial, release also noted Tourette trials, of States. about in we XXX these eighteen twelve this other study. this that the is is on from approximately randomize is clinicaltrials.gov. those it syndrome higher patients of so design week, portion. the doses trial a who excited open one with We study anticipate press of can and blind enroll. of as the includes will double treatment weeks one to age. used Phase top-line that aged for extension as includes all randomized are obviously an and in strategy trial United through recruitment in Like were the label GOLD that's for on dependent to huge progress XXXX, those very on trial The
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month to approximately FDA would provide As then meeting face minutes the usual meetings, with meeting. formal face after these the one
that. So we'll keep updated on you
with As quality has in to of a beginning Kevin progress have range high publications. mentioned, but made across happy are partners scientific job generating not share data, really They elagolix AbbVie. tremendous and we by meetings now been a the with data that that only our done
they’re recently, of data into treatment. about The long-term won't Journal out So England through of rolling pivotal months and Medicine efficacy really the out after twelve And now all go publication additional details in New the safety the I abstracts.
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work. to a AbbVie our such at for So congrats outstanding colleagues
the programs that’s active forward in questions. that look the and with turn to to So clinic. currently I'll it an that five update on Kevin are back your