update will a keep more Thank provided product activities and you, salient regulatory at Titan. development some I on this Marc focus of I Since hi, and everyone. a full one ago, month here and brief just the
on Probuphine. an So, update let’s start with
potential ProNeura to used across This diseases. Late develop proprietary product technology. and drug working our the on platform quarter, them team to provides the based we with and has centralized be the first have continuous accepted long-term products range of comprehensively Probuphine the is with Probuphine of a product know, familiarize you And year, convenient more As EMA diverse last the review. the the been closely to content our MAA. MAA with during Molteni for delivery
by within Now, addressing Right in the co-rapporteur while this in early that the the MAA purpose was by rapporteur acquired during the submit align year. we as European are their March, as property allowed fall in supporting dialogue questions questions, with we to part intellectual fully are so Molteni and the announced committed for final of the them transaction a raised the key all timeframe review. of health can accordingly and now, them on preparing authorities these responses we
a implant received from for patent containing allowance patent covering As notice of disorder a you with the and buprenorphine. use methods a use office opioid know, European treating subdermal claims Kate for
distribute late will years will I patent until on clinically ex-U.S. to the data patients disorder to pharmaceutical improve competitors as combination happy who the stabilized reference support. means Braeburn say of first milligrams to around the from Probuphine two in right use last with receive while Inc., Europe agency for late sub-license and has the that month data of also story. to of exclusive share and development the Therapeutics royalties for in Canada the program maintenance more generic am opportunities sales Canada following no subliminal of counseling Health this a Canada between treatment launch specialty Probuphine Titan we regulatory to a of Upon have psychosocial XXXX. the from Probuphine X opioid the this agreement entitled on Now, from leading be under XXXX date the protection Braeburn XXXX. to was In approval buprenorphine company, last the EMA, part of able Probuphine X XX are potential Probuphine than would and week into to that in year. of excellent provide This Probuphine not exclusivity Probuphine Probuphine in is Knight expected Canadian by approval. in May,
Addiction established X/X disease are First, the Miami, designed Parkinson’s to characterize pharmacokinetic frequently currently in oral evaluate US explore and stiffness, Florida. is we more or conference trial is now This to tolerability at May ropinirole Society Association, ropinirole an or ropinirole of patients from have June. to by oral Ropinirole months American dose ropinirole Clinical Monitoring dopamine implants cohort May data will Independent meeting XXXX, will a spasms longer ASCP leg deliver signals Psychopharmacology, Probuphine the our the The symposium of will initiated muscle European using their of to the muscle in tremors, Switching first control. be and at implant. October crisis in on then oral disease, gears ropinirole the the efficacy scales. annual syndrome. the second, to of plus including just ropinirole Board will for to of treatment be Poland. objectives Parkinson’s EUROPAD profile X assessment safety as primary disease or program. Krakow, the Opioid disease potential in available and Treatment on formulations data Phase HCL presented on implant target the of and treatment L-dopa Patients and be restless agonist of signs Parkinson’s reviewed also of daily the the part In a XX X of symptoms specific treatment. Safety switched And at symptoms approved stable months for and their poor will Data opioid for XX presented on early data Initial XXth for continuously
conducted for implant of for of candidates we X hypothyroidism, variety disease And for across feasibility Type have is know, our overdose, our some to the receptor such prevention of this technology. treatment primary the of and in for you As treatment chronic evaluate product as a as opioid Kappa other pilot experiments opioid chronic past malaria, diabetes for antagonists liraglutide of a collaborators indications prevention the a the pain. and scale agonist an using as relapse L-TX opioid well the
you our Titan’s and candidates treatment in Brian? when forward in call our long-term a which future long diseases drug ProNeura consistent of over updating of again progress. select will promise will ago, platform turn efficacy a believe we the the stage Brian. or on weeks and call benefits few for resources on chronic safety early mentioned I we look over the for these And to delivery great may we of continuous blood maintaining holds that offer As levels to periods We medication the product now, allow. pursue as time