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Prilenia Therapeutics B.V.: Prilenia receives positive EMA opinion on Orphan Drug Designation for pridopidine in ALS finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.
Prilenia Therapeutics: Prilenia Achieves 25% Enrollment in its Phase 3 HD Trial and Appoints Dr. Goldberg as CSO PROOF-HD is the most advanced clinical trial in HD assessing impact on clinical progression Dr. Y Paul Goldberg joins Prilenia to enhance the broader scientific strategy for pridopidine Prilenia Therapeutics B.V., a clinical stage biotech company focused on developing novel treatments for neurodegenerative and neurodevelopmental disorders, is pleased to announce that it has now enrolled more than 120 patients in its Phase 3 trial of pridopidine in HD (PROOF-HD), reaching 25% of the total target enrollment. The study remains on target to complete enrollment by Q4 2021 as originally planned. ....
Prilenia Enrolls First Subject in Europe in its PROOF-HD Phase 3 Clinical Trial for Huntington s Disease About Prilenia (www.prilenia.com) Prilenia is a clinical stage biotech startup founded in 2018 with the purpose of improving the lives of patients and their families by developing treatments for neurodegenerative and neurodevelopmental disorders. Prilenia raised 88.5 million thus far and is backed by a group of well-respected investors: Talisman, Forbion, Morningside and Sectoral and ALS Investment Fund. The Company is based in Naarden, the Netherlands, Herzliya, Israel and Boston, MA in the U.S. About Pridopidine Prilenia s lead asset is Pridopidine, a first-in-class drug candidate with an established safety profile and therapeutic potential in several neurodegenerative diseases affecting adults and children. The highly selective S1R agonist was acquired from Teva in 2018. ....
Press release content from Business Wire. The AP news staff was not involved in its creation. Prilenia Announces First Patient Enrolled for Pridopidine Phase 2/3 Platform Trial for ALS January 8, 2021 GMT NAARDEN, The Netherlands (BUSINESS WIRE) Jan 8, 2021 Prilenia Therapeutics B.V., a clinical stage biotech company focused on developing novel treatments for neurodegenerative and neurodevelopmental disorders, today announces the enrollment of the first participant for treatment with pridopidine in the pivotal HEALEY ALS Platform Trial. The HEALEY ALS Platform trial (“HEALEY trial”; NCT04297683 ) is a multi-center, multi-regimen clinical trial evaluating the safety and efficacy of investigational products for the treatment of amyotrophic lateral sclerosis (ALS). It is the first platform trial for ALS, designed to accelerate development of promising new treatments by enabling investigators to simultaneously assess multiple therapeutic candidates. ....
(1) Pridopidine was chosen in global competition as one of the top drug candidates to participate in the first ever ALS Platform Trial led by the Healey Center at Massachusetts General Hospital This trial is the second late-stage clinical trial in neurodegenerative disorders with pridopidine, in addition to the global Phase 3 trial in Huntington s disease Positive data from this clinical study could lead to registration of pridopidine for the treatment of ALS Prilenia Therapeutics B.V., a clinical stage biotech company focused on developing novel treatments for neurodegenerative and neurodevelopmental disorders, today announces the enrollment of the first participant for treatment with pridopidine in the pivotal HEALEY ALS Platform Trial. ....