Brief: Ascletis Pharma Inc Announces IND Approval By U.S. FDA For Development Of Asc22 (Envafolimab)
17/01/2022 12:44
Jan 17 (Reuters) - Ascletis Pharma Inc 1672.HK :
* ANNOUNCES INVESTIGATIONAL NEW DRUG APPLICATION APPROVAL BY
U.S.
FDA FOR DEVELOPMENT OF CO'S ASC22 (ENVAFOLIMAB)
Further company coverage: 1672.HK
((Reuters.Briefs@thomsonreuters.com;))
Recent news on Ascletis Pharma
See all newsFactbox: Race to launch weight-loss pill heats up as Novo wins UK approval
Brief: Ascletis Announces Fixed-Dose Combination of ASC30, Once-Daily Oral Small Molecule GLP-1R Agonist, and ASC39, Once-Daily Oral Small Molecule Amylin-Selective Amylin Receptor Agonist, for Clinical Development
Factbox: Race to launch weight-loss pill heats up as Lilly wins US approval
Brief: Ascletis Pharma FY Loss Attributable Rmb359.9 Million
Brief: Ascletis Pharma Expects To Submit IND Application To U.S. FDA For ASC39 In Q3 2026