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OncoMatch/Clinical Trials/NCT07353957

Study to Investigate Petosemtamab in Adults With Metastatic Non-Small Cell Lung Cancer

Is NCT07353957 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Petosemtamab + Pembrolizumab for lung cancer - non small cell squamous.

Phase 2RecruitingMerus B.V.NCT07353957Data as of May 2026

Treatment: Petosemtamab + PembrolizumabThe study will test the efficacy and safety of petosemtamab in combination with Pembrolizumab in first line patients with squamous non-small cell lung cancer and non-squamous non-small cell lung cancer.

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Extracted eligibility criteria

Biomarker criteria

Required: PD-L1 (CD274) TPS ≥ 50% (TPS ≥ 50%)

PD-L1 TPS ≥ 50%

Disease stage

Required: Stage IV

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: PD-(L)1 inhibitor

Participants who received prior treatment with a PD-(L)1 inhibitor

Cannot have received: systemic chemotherapy

Participants who have received prior systemic chemotherapy, targeted or biological antineoplastic therapy for metastatic NSCLC

Cannot have received: targeted therapy

Participants who have received prior systemic chemotherapy, targeted or biological antineoplastic therapy for metastatic NSCLC

Cannot have received: biological antineoplastic therapy

Participants who have received prior systemic chemotherapy, targeted or biological antineoplastic therapy for metastatic NSCLC

Cannot have received: systemic anticancer therapy

Any systemic anticancer therapy within 4 weeks prior to the first dose of study treatment

Cannot have received: radiotherapy

Exception: Participants who received prior radiotherapy to ≥ 25% of bone marrow are not eligible, regardless of when it was received.

Major surgery or radiotherapy within 3 weeks prior to the first dose of study treatment. Participants who received prior radiotherapy to ≥ 25% of bone marrow are not eligible, regardless of when it was received.

Lab requirements

Blood counts

adequate hematologic function

Kidney function

creatinine clearance ≥ 60 ml/min calculated according to the cockroft and gault formula

Liver function

adequate liver function

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

US trial sites

  • Tennessee Site 2 · Chattanooga, Tennessee
  • Tennessee Site 1 · Nashville, Tennessee
  • Virginia Site 1 · Fairfax, Virginia

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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