Single Agent Envafolimab ORR Exceeded Futility Rule that will be Applied at the Interim Efficacy Analysis Expected in Q3 Continuing Double-Digit Objective Response Rate (ORR) by Blinded...
Biocytogen Pharmaceuticals and Tracon Pharmaceuticals have obtained clearance for the Investigational New Drug (IND) application from the US Food and Drug Administration (FDA) to begin the Phase I/II clinical trial of YH001 plus envafolimab and doxorubicin to treat sarcoma patients.
HANGZHOU, China and SHAOXING, China, Feb. 14, 2022 /PRNewswire/ -- Ascletis Pharma Inc. (HKEX: 1672) today announces that Shanghai Public Health Clinical Center initiated functional cure study of anti-PD-L1 antibody ASC22 (Envafolimab) in combination with Chidamide in patients infected by human immunodeficiency virus (HIV) with antiviral suppression.