SAGE Therapeutics reports positive top-line results from phase 2 placebo-controlled trial of SAGE-217
- SAGE-217 met primary endpoint and provided rapid, profound and durable effects through 2-week treatment period and additional 4-week follow-up
- Well-tolerated and demonstrated highly statistically significant mean reduction in the HAM-D score compared to placebo at 15 days beginning after one dose and maintained through Week 4 with numerical superiority though Week 6
- All secondary endpoints were consistent with primary endpoints at Day 15, including remission in 64% of SAGE-217 patients versus 23% of placebo patients
- Data support further development of SAGE-217 for MDD and related disorders
No comments:
Post a Comment