Sage Therapeutics, Inc. and partner Biogen, Inc. revealed on 24 July that SAGE-324, a positive allosteric modulator (PAM) of the GABA-A receptor, did not meet the primary endpoint in a Phase II dose-ranging study in essential tremor (ET). The clinical trial failure is Sage’s second mid-stage upset this year and the setback eliminates a needed later-stage program from Biogen’s pipeline.
Key Takeaways
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Sage and Biogen will discontinue development of SAGE-324 in essential tremor after all doses of the drug failed on the primary endpoint in the Phase II...
The companies said they will end development of SAGE-324 in ET while evaluating next steps in other potential indications. Analysts said in same-day notes that they viewed the Phase II...
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