drugset / Trial / NCT04471415

Study to Investigate DRP-104 in Adults With Advanced Solid Tumors

NCT04471415

Phase 1/2 Terminated 61 enrolled Dracen Pharmaceuticals, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to characterize the safety, tolerability, pharmacokinetics, pharmaco-dynamics and preliminary anti-tumor activity of DRP-104 (sirpiglenastat) administered via intravenous infusion or via subcutaneous injection as a single agent and in combination with atezolizumab in patients with advanced solid tumors and to assess preliminary safety and efficacy of which route of administration (intravenous or subcutaneous) will be selected for further development for the one expansion of patients, advanced non-small cell lung cancer (NSCLC) with defined genetic mutations.

Timeline

Start
2020-08-31
Primary completion
2023-03-28
Completion
2023-03-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Atezolizumab Monoclonal antibody 1200 mg Intravenous
Subject sirpiglenastat Small molecule 3.3 mg/m2 Intravenous
Subject sirpiglenastat Small molecule 10 mg Intravenous