drugset / Trial / NCT03583086

Phase I/II Eval Safety & Prelim Activity Nivolumab Comb W/Vorolanib Pts W/Refractory Thoracic Tumors

NCT03583086

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a two-agent, open-label, non-randomized, Phase 1/2 dose escalation and dose expansion study of combinatorial oral vorolanib plus infusional nivolumab in patients with Non-Small Cell Lung Cancer naïve to checkpoint inhibitor therapy, Non-Small Cell Lung Cancer who have progressed on checkpoint inhibitor therapy, Small Cell Lung Cancer ( who have progressed on platinum-based chemotherapy, and thymic carcinoma.

Timeline

Start
2018-07-10
Primary completion
2024-02-21
Completion
2024-04-27

Drugs

EvaluationDrugModalityDoseRoute
Subject CM082 Unknown Oral
Subject Nivolumab Monoclonal antibody Intravenous