June 24 (Reuters) - TuHURA Biosciences Inc HURA.O:
TUHURA BIOSCIENCES INITIATES ITS PHASE 3 ACCELERATED APPROVAL TRIAL OF IFX-2.0 AS AN ADJUNCTIVE THERAPY TO KEYTRUDA® (PEMBROLIZUMAB) IN FIRST LINE TREATMENT FOR ADVANCED OR METASTATIC MERKEL CELL CARCINOMA
TUHURA BIOSCIENCES INC: PRIMARY ENDPOINT OF OVERALL RESPONSE RATE $(ORR.AU)$ QUALIFIES FOR ACCELERATED APPROVAL PROCESS
TUHURA BIOSCIENCES INC -KEY SECONDARY ENDPOINT OF PROGRESSION FREE SURVIVAL $(PFS)$ MAY SATISFY REQUIREMENT FOR A POST CONFIRMATORY TRIAL
Source text: ID:nPn3sVmWSa
Further company coverage: HURA.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。