Prilenia and Ferrer initiate PRECISE-HD study for Huntington’s disease
The confirmatory trial will evaluate pridopidine in 400 participants across 75 sites, with a 52-week placebo-controlled stage and 104-week open-label extension.
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Clinical-stage biotech developing neurodegenerative disease treatments
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In short: Prilenia and Ferrer initiated the Phase 3 PRECISE-HD and PREVAiLS studies to evaluate pridopidine in Huntington's disease and ALS.
The confirmatory trial will evaluate pridopidine in 400 participants across 75 sites, with a 52-week placebo-controlled stage and 104-week open-label extension.
The data from placebo arms of PRIDE and PROOF studies will advance Huntington's disease research.
The study evaluates pridopidine in ALS, with first Canadian patient enrolled and global recruitment across 13 countries.
Eric Litjens emphasizes harnessing biotech innovation for economy, healthcare leadership, and patient outcomes in rare neurodegenerative diseases like ALS and Huntington's.
NAARDEN, Netherlands & WALTHAM, Mass. & BARCELONA, Spain, July 07, 2026--Prilenia Therapeutics B.V. and Ferreri today announced initiation of the confirmatory PRECISE-HD study (Pridopidine Phase...
Prilenia Therapeutics B.V., a biopharmaceutical company driven by an unwavering commitment to scientific excellence and accelerating progress for people affected by Huntington's disease (HD) and...
The “PREVAiLS” study, which will review the investigational drug pridopidine as a potential ALS treatment, has already enrolled its first participant, according to a press...
Prilenia Therapeutics and Ferrer have enrolled the first participant in the Phase III PREVAiLS trial assessing pridopidine in early ALS.
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