The company revealed the findings at a London medical conference, confirming that the treatment was well tolerated in the study. By targeting both intracellular and extracellular tau—a protein linked to neuronal health in the central nervous system—the therapy demonstrated sustained efficacy during the observation period. The U.S. Food and Drug Administration granted investigational new drug clearance for the candidate in June, paving the way for upcoming trials.
In section Market Quotes
Voyager Therapeutics Clears Hurdle for Alzheimer’s Gene Therapy
A single intravenous dose of VY1706 reduced tau protein levels by up to 75% in non-human primates over six months, according to new toxicology data. Following these results, Voyager Therapeutics intends to move its investigational gene therapy into human clinical trials for early-stage Alzheimer’s disease later this year.

Chief Executive Alfred Sandrock stated that the data reinforces the pharmacology and durability observed in earlier testing. Voyager remains focused on the potential of tau as a therapeutic target for neurodegenerative decline. Investors responded to the announcement with a 3.3% uptick in premarket trading, pushing shares to $3.55, a modest recovery after the stock’s 12% decline earlier this year.
Comments (0)
No comments yet. Be the first!