Antengene Receives the US FDA’s IND Clearance of ATG-031 for Advanced Solid Tumors or B-Cell Non-Hodgkin's Lymphoma
Shots:
- The US FDA has cleared an IND application to initiate the P-I (PERFORM) dose-finding study of ATG-031 for advanced solid tumors or B-NHL
- The primary objective of the study is to evaluate ATG-031's safety & tolerability as a monotx. and to select the right dose for P-II studies while the secondary objective is to characterize ATG-031's pharmacology, examine its immunogenicity & evaluate the preliminary efficacy
- ATG-031, a humanized anti-CD24 mAb, blocks the "don't eat me" signal in the TME. The goal of the treatment is to increase macrophage-mediated phagocytosis of cancer cells & improve the activity of cytotoxic T cells in TME by binding with the CD24 expression on cancer cells with high affinity & blocking the connection b/w CD24 & Siglec-10 receptor
Ref: PRNewswire | Image: Antengene
Related News:- Antengene Entered into a Clinical Collaboration with MSD to Evaluate ATG-037 + Keytruda (pembrolizumab) for Solid Tumors
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