Nov 20 (Reuters) - SAGE Therapeutics Inc SAGE.O:
SAGE THERAPEUTICS ANNOUNCES TOPLINE RESULTS FROM THE PHASE 2 DIMENSION STUDY OF DALZANEMDOR (SAGE-718) IN THE TREATMENT OF COGNITIVE IMPAIRMENT ASSOCIATED WITH HUNTINGTON’S DISEASE
SAGE THERAPEUTICS INC - DALZANEMDOR DID NOT MEET PRIMARY ENDPOINT IN PHASE 2 STUDY
SAGE THERAPEUTICS INC - DALZANEMDOR GENERALLY WELL-TOLERATED WITH NO NEW SAFETY SIGNALS
SAGE THERAPEUTICS INC - TO HALT FURTHER DEVELOPMENT OF DALZANEMDOR
SAGE THERAPEUTICS - TO CLOSE ONGOING PURVIEW STUDY, AN OPEN-LABEL SAFETY STUDY OF DALZANEMDOR IN PARTICIPANTS WITH HD
Source text: ID:nBw3XvSsba
Further company coverage: SAGE.O
((Reuters.Briefs@thomsonreuters.com;))
免責聲明:投資有風險,本文並非投資建議,以上內容不應被視為任何金融產品的購買或出售要約、建議或邀請,作者或其他用戶的任何相關討論、評論或帖子也不應被視為此類內容。本文僅供一般參考,不考慮您的個人投資目標、財務狀況或需求。TTM對信息的準確性和完整性不承擔任何責任或保證,投資者應自行研究並在投資前尋求專業建議。