drugset / Trial / NCT03061539

Nivolumab and Ipilimumab Treatment in Prostate Cancer With an Immunogenic Signature

NCT03061539 ↗

Phase 2 Active not recruiting 380 enrolled University College, London Bristol-Myers Squibb · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objective is to test the following hypothesis: Patients with metastatic castrate resistant prostate cancer that have progressed following at least one line of therapy and have an immunogenic signature will respond to combined PD-1 and CTLA4 inhibition.

Timeline

Start
2018-02-06
Primary completion
2022-06-20
Completion
2027-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody 1 mg/kg —
Subject Ipilimumab Monoclonal antibody 3 mg/kg —
Subject Nivolumab Monoclonal antibody 480 mg —

Indications