Sage Therapeutics' dalzanemdor (SAGE-718) failed to meet key goals in a Phase 2 study for cognitive impairment in Huntington's disease, leading to the program's discontinuation.
The Phase 2 KINETIC 2 study of SAGE-324 (BIIB124) did not meet its primary endpoint of demonstrating a statistically significant dose-response relationship in essential tremor patients.
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