10:58 PM EST, 01/01/2023 (MT Newswires) -- The US Food and Drug Administration allowed 3D Medicines (HKG:1244) to proceed with its Phase II study for envafolimab for the treatment of mismatch repair deficiency advanced solid tumors, according to a filing on Friday.
The trial, which is a multiregional, multicenter, single-arm study, will assess the efficacy and safety of envafolimab
monotherapy in advanced solid tumors.
The drug will be administrated to the patients subcutaneously every three weeks.