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- In the Phase 2 PRECEDENT Study, dalzanemdor (SAGE-718) did not show statistically significant differences versus placebo on the primary endpoint in patients with mild cognitive impairment in Parkinsons disease
- Dalzanemdor (SAGE-718) was generally well-tolerated and there were no new safety signals observed
- Topline data readouts from the Phase 2 studies in Huntingtons disease and Alzheimers disease are expected later this year
CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Sage Therapeutics, Inc. (Nasdaq: SAGE) announced today topline results from PRECEDENT, a double-blind, placebo-controlled Phase 2 study of the... More

