drugset / Trial / NCT03502746

Phase II Nivolumab and Ramucirumab for Patients With Previously-Treated Mesothelioma

NCT03502746 ↗

NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the combination of Nivolumab and Ramucirumab in patients with previously-treated mesothelioma.

Timeline

Start
2018-06-26
Primary completion
2022-05-11
Completion
2023-11-09

Outcome

Missed primary endpoint

Stopped: “IRB Study Closure”

paper The primary end point of 40% ORR was not reached. PMID 38046376 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 240 mg Intravenous
Subject Ramucirumab Monoclonal antibody 8 mg/kg Intravenous