drugset / Trial / NCT05576961

Safety and Efficacy of RX-af01 Combined With PD-1 Antibody

NCT05576961

Phase 1/2 Unknown 60 enrolled Sun Yat-sen University
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This phase I trial evaluates the effects of RX-af01 in combination with toripalimab (PD-1 antibody), in treating patients with refractory advanced solid tumors, including melanoma, nasopharyngeal squamous carcinoma, esophageal squamous cell carcinoma, gastric adenocarcinoma, renal cell carcinoma, et al. RX-af01 is a kind of anti-tumor intestinal bacteria developed by our research group. Its main components are symbiotic bacteria from human intestine - Alisipes finegoldii (A. finegoldii.), which is a Gram negative anaerobic bacteria. Our previous research shows that A finegoldii. can significantly enhance the anti-tumor activity of PD-1 antibody in multiple mouse tumor models. Mechanism research shows that A finegoldii. can increase the infiltration of CD4 and CD8 positive immune cells in the tumor microenvironment, and enhances the anti-tumor activity of immune cells. The primary aim of this study is to explore the efficacy and safety of RX-af01 combined with PD-1 antibody in refractory advanced solid tumors.

Timeline

Start
2022-09-15
Primary completion
2024-12-31
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject High dose RX-af01 Other / unclassified
Subject RX-af01 Other / unclassified Oral
Background Toripalimab Monoclonal antibody
Background Toripalimab Monoclonal antibody 240 mg Intravenous
Background Vancomycin Other / unclassified 125 mg Oral

Indications