April 25 (Reuters) - EMA:
EMA SAYS CHMP WILL RE-EXAMINE OPINION ADOPTED FOR MARKETING AUTHORISATION HOLDER FOR KISUNLA (DONANEMAB)
EMA SAYS CHMP RECOMMENDS CONDITIONAL MARKETING AUTHORISATION FOR DUVYZAT (GIVINOSTAT), AS TREATMENT FOR DMD IN PATIENTS FROM AGE SIX WHO CAN WALK
EMA SAYS TEPEZZA (TEPROTUMUMAB) RECEIVED POSITIVE OPINION FROM CHMP FOR TREATMENT OF ADULTS WITH MODERATE TO SEVERE THYROID EYE DISEASE
EMA SAYS SEPHIENCE (SEPIAPTERIN) GOT POSITIVE OPINION FROM CHMP FOR TREATMENT OF HYPERPHENYLALANINAEMIA IN ADULTS & CHILDREN WITH PHENYLKETONURIA
EMA SAYS CHMP RECOMMENDED GRANTING CONDITIONAL MARKETING AUTHORISATION FOR ZIIHERA (ZANIDATAMAB)
Source text: [ID:]
Further company coverage: LLY.N
((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。