drugset / Trial / NCT05043714

Study of NG-641 in Combination With Nivolumab in Metastatic or Advanced Epithelial Tumours

NCT05043714

Phase 1 Completed 30 enrolled Akamis Bio Bristol-Myers Squibb · collab
NaSequentialOpen-labelTreatment

Summary

This is a phase 1a/1b, multicentre, open-label, non-randomized study of NG-641 in combination with nivolumab (or standard of care PD-1 inhibition) in patients with metastatic or advanced epithelial tumours. The purpose is to characterize the safety and tolerability of NG-641 in combination with nivolumab in patients with metastatic or advanced epithelial tumours and to determine the recommended dose of NG-641 in combination with nivolumab for further development in patients with metastatic or advanced epithelial tumours

Timeline

Start
2021-12-01
Primary completion
2023-11-13
Completion
2024-10-04

Drugs

EvaluationDrugModalityDoseRoute
Subject NG-641 Unknown Intravenous
Background Nivolumab Monoclonal antibody