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OncoMatch/Clinical Trials/NCT03760575

Pembrolizumab in Combination With Chemotherapy and Image-Guided Surgery for Malignant Pleural Mesothelioma (MPM)

Is NCT03760575 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including Pembrolizumab and Cisplatin for mesotheliomas pleural.

Phase 1RecruitingAbramson Cancer Center at Penn MedicineNCT03760575Data as of May 2026

Treatment: Pembrolizumab · Cisplatin · PemetrexedThe study is a single-arm phase I trial to evaluate the safety, feasibility, and preliminary efficacy of the addition of pembrolizumab and image-guided resection to surgical therapy and chemotherapy for malignant pleural mesothelioma (MPM).

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Extracted eligibility criteria

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: anti-PD-1/PD-L1/PD-L2 agent

Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

Cannot have received: anti-cancer monoclonal antibody

Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to agents administered more than 4 weeks earlier.

Cannot have received: chemotherapy

Exception: ≤ Grade 2 neuropathy are an exception

Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to a previously administered agent.

Cannot have received: targeted small molecule therapy

Exception: ≤ Grade 2 neuropathy are an exception

Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to a previously administered agent.

Cannot have received: radiation therapy

Exception: ≤ Grade 2 neuropathy are an exception

Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to a previously administered agent.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Abramson Cancer Center of the University of Pennsylvania · Philadelphia, Pennsylvania

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