drugset / Trial / NCT03918252

Neoadjuvant Immune Checkpoint Blockade in Resectable Malignant Pleural Mesothelioma

NCT03918252 ↗

Non-randomizedSequentialOpen-labelTreatment

Summary

The proposed study will evaluate the safety and feasibility of neoadjuvant nivolumab +/- ipilimumab in resectable MPM. In addition, maintenance nivolumab will be administered for 1 year following completion of standard bi-/tri-modality therapy.

Timeline

Start
2019-10-02
Primary completion
2027-06
Completion
2028-06

Outcome

Met primary endpoint

paper The trial met its primary endpoints PMID 40921804 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody 1 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 3 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 240 mg Intravenous