Prilenia’s Pridopidine for Huntington’s Disease Accepted for European Marketing Authorisation Review

Prilenia, a clinical stage biotechnology company focused on the urgent mission to develop novel therapeutics to slow the progression of neurodegenerative diseases and neurodevelopmental disorders, has filed a European Marketing Authorization Application (MAA) with the European Medicines Agency (EMA) for pridopidine as a treatment for Huntington’s disease (HD). An MAA Loe edasi...

IROS, Prilenia and International Huntington’s Disease Association collaborate on first-ever Huntington’s disease (HD) trial in the MENA region

Abu Dhabi, UAE; June 19, 2024: IROS, an Abu Dhabi-based contract research organization (part of the M42 group), has partnered with Prilenia Therapeutics, a clinical-stage biotech company, and the International Huntington’s Disease Association (IHA) to plan the first-ever clinical trial for Huntington’s disease (HD) in the UAE and MENA region, Loe edasi...

uniQure Announces Positive Interim Data Update Demonstrating Slowing of Disease Progression in Phase I/II Trials of AMT-130 for HD

“We are very pleased with these new data demonstrating a statistically significant, dose-dependent slowing of the progression of Huntington’s disease and lowering of NfL in the CSF at 24 months,” stated Walid Abi-Saab, M.D., chief medical officer of uniQure. “We believe this is the first clinical trial of any investigational medicine Loe edasi...

Wave Life Sciences annab teada positiivsetest tulemustest faasi 1b/2a uuringust SELECT-HD, mis näitab esmakordselt kliiniliselt, et Huntingtoni tõve all-selektiivne mutant Huntingtin vähendab Huntingtoni tõbe

Täna teatas Wave Life Sciences positiivsetest tulemustest SELECT-HD, meie platseebokontrolliga faasi 1b/2a uuringust, milles hinnatakse uuritavat ravi WVE-003. Need tulemused näitavad, et WVE-003 vähendab selektiivselt toksilist, mutantset huntingtiini (mHTT) valku ja säilitab terve, metsikut tüüpi huntingtiini (wtHTT) valgu Huntingtoni tõvega isikute puhul. Uuringu tulemusedAnalüüsis võrreldi Loe edasi...

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