Brief: Antengene Says U.S. FDA Ind Clearance For Phase I Trial Of Atg-017
Oct 31 (Reuters) - Antengene Corporation Ltd 6996.HK :
* U.S. FDA IND CLEARANCE FOR PHASE I TRIAL OF- SMALL
MOLECULE
ERK1/2 INHIBITOR ATG-017 IN- PATIENTS WITH ADVANCED SOLID TUMORS
* INVESTIGATIONAL NEW DRUG APPLICATION FOR ATG-017 HAS
RECEIVED
CLEARANCE FROM U.S. FDA
Further company coverage: 6996.HK
((Reuters.Briefs@thomsonreuters.com;))
Recent news on Antengene
See all newsBiotech firm Antengene's H1 revenue jumps on licensing deals
Brief: Antengene Corp Expects HY Profit Of RMB195 MLN-RMB238 MLN
Brief: Antengene Corp Receives Initial $60 Million Upfront Payment From UCB
Brief: Antengene Corp Intends To Repurchase Up To 67.92 Million Shares
Brief: Antengene Corp Enters Exclusive License Agreement With K2 Therapeutics For Atg-106