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OncoMatch/Clinical Trials/NCT06623422

A Study of Pembrolizumab (MK-3475) With or Without Intismeran Autogene (V940) in Participants With Non-small Cell Lung Cancer (V940-009/INTerpath-009)

Is NCT06623422 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments for carcinoma, non-small-cell lung.

Phase 3RecruitingMerck Sharp & Dohme LLCNCT06623422Data as of May 2026

Treatment: Pembrolizumab · Cisplatin · Carboplatin · Pemetrexed · Gemcitabine · Paclitaxel · Intismeran autogeneThe goal of this study is to learn if people who receive intismeran autogene and pembrolizumab after surgery are cancer-free longer than people who receive placebo and pembrolizumab. Researchers want to know if giving intismeran autogene and pembrolizumab after surgery can help prevent the cancer from coming back in people with non-small cell lung cancer (NSCLC) whose tumors did not respond completely to treatment before surgery (neoadjuvant treatment).

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: EGFR wild-type

documentation of absence of tumor-activating EGFR mutations [eg, DEL19 or L858R]

Excluded: ALK rearrangement

presence of anaplastic lymphoma kinase (ALK) gene rearrangements

Disease stage

Required: Stage II, IIIA, IIIB (N2)

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

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

Cannot have received: neoadjuvant therapy

Exception: except as specified in protocol (neoadjuvant chemotherapy and pembrolizumab followed by surgery allowed if no pCR)

Received prior neoadjuvant therapy for their current NSCLC diagnosis

Cannot have received: anti-PD-1/PD-L1/PD-L2 or co-inhibitory T-cell receptor therapy

Received prior therapy with an anti-programmed cell death 1 (PD-1), anti-programmed cell death ligand 1 (PD-L1), or anti-programmed cell-death ligand 2 (PD-L2) agent, or with an agent directed to another stimulatory or coinhibitory T-cell receptor (eg, cytotoxic T-lymphocyte-associated protein [CTLA-4], OX-40, CD137)

Cannot have received: systemic anticancer therapy

Exception: other than what is specified in this protocol

Received prior systemic anticancer therapy including investigational agents other than what is specified in this protocol

Cannot have received: cancer vaccine

Received prior treatment with a cancer vaccine

Cannot have received: radiation therapy

Exception: within 2 weeks of start of study intervention, or has radiation-related toxicities, requiring corticosteroids

Received prior radiotherapy within 2 weeks of start of study intervention, or has radiation-related toxicities, requiring corticosteroids

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

US trial sites

  • Banner MD Anderson Cancer Center ( Site 0181) · Gilbert, Arizona
  • The University of Arizona Cancer Center - North Campus ( Site 0163) · Tucson, Arizona
  • Providence St. Jude Medical Center ( Site 0106) · Fullerton, California
  • VA Long Beach Healthcare System ( Site 0199) · Long Beach, California
  • USC Norris Comprehensive Cancer Center ( Site 0205) · Los Angeles, California

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

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