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OncoMatch/Clinical Trials/NCT06116786

A Study of JNJ-86974680 in Participants With Advanced Non-small Cell Lung Cancer

Is NCT06116786 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies multiple treatments including JNJ-86974680 and Cetrelimab for carcinoma, non-small-cell lung.

Phase 1RecruitingJohnson & Johnson Enterprise Innovation Inc.NCT06116786Data as of Jun 2026Location: International · 4 countries

Treatment: JNJ-86974680 · CetrelimabThe purpose of this study is to determine a safe and tolerable dose(s) of JNJ-86974680 for further research in combination with cetrelimab and radiation therapy.

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Extracted eligibility criteria

Treatments studied

Other

JNJ-86974680Cetrelimab

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: EGFR wild-type

No targetable mutations (for example, EGFR [epidermal growth factor receptor], ALK [anaplastic lymphoma kinase], ROS1[c-ros oncogene 1], and BRAF [B-Raf proto-oncogene, serine/threonine kinase])

Required: ALK wild-type

No targetable mutations (for example, EGFR [epidermal growth factor receptor], ALK [anaplastic lymphoma kinase], ROS1[c-ros oncogene 1], and BRAF [B-Raf proto-oncogene, serine/threonine kinase])

Required: ROS1 wild-type

No targetable mutations (for example, EGFR [epidermal growth factor receptor], ALK [anaplastic lymphoma kinase], ROS1[c-ros oncogene 1], and BRAF [B-Raf proto-oncogene, serine/threonine kinase])

Required: BRAF wild-type

No targetable mutations (for example, EGFR [epidermal growth factor receptor], ALK [anaplastic lymphoma kinase], ROS1[c-ros oncogene 1], and BRAF [B-Raf proto-oncogene, serine/threonine kinase])

Allowed: EGFR actionable mutation

NSCLC with a known actionable genetic mutation (for example, epidermal growth factor receptor [EGFR], anaplastic lymphoma kinase [ALK], c-ros oncogene 1 [ROS1], v-raf murine sarcoma viral oncogene homolog B1 [BRAF]) must have received all approved targeted therapies and have progressed

Allowed: ALK actionable mutation

NSCLC with a known actionable genetic mutation (for example, epidermal growth factor receptor [EGFR], anaplastic lymphoma kinase [ALK], c-ros oncogene 1 [ROS1], v-raf murine sarcoma viral oncogene homolog B1 [BRAF]) must have received all approved targeted therapies and have progressed

Allowed: ROS1 actionable mutation

NSCLC with a known actionable genetic mutation (for example, epidermal growth factor receptor [EGFR], anaplastic lymphoma kinase [ALK], c-ros oncogene 1 [ROS1], v-raf murine sarcoma viral oncogene homolog B1 [BRAF]) must have received all approved targeted therapies and have progressed

Allowed: BRAF actionable mutation

NSCLC with a known actionable genetic mutation (for example, epidermal growth factor receptor [EGFR], anaplastic lymphoma kinase [ALK], c-ros oncogene 1 [ROS1], v-raf murine sarcoma viral oncogene homolog B1 [BRAF]) must have received all approved targeted therapies and have progressed

Disease stage

Required: Stage IIIB, IV

Prior therapy

Must have received: targeted therapy — all approved targeted therapies for actionable mutations

must have received all approved targeted therapies and have progressed

Must have received: anti-PD-1 therapy

Must have been treated with (a) anti-programmed death protein 1 (anti-PD-1) or programmed cell death ligand 1 (PD-L1) therapy

Must have received: anti-PD-L1 therapy

Must have been treated with (a) anti-programmed death protein 1 (anti-PD-1) or programmed cell death ligand 1 (PD-L1) therapy

Must have received: platinum-based chemotherapy

Must have been treated with ... (b) platinum-based chemotherapy

Lab requirements

Blood counts

Kidney function

Liver function

Adequate organ function

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

US trial sites

  • City of Hope · Newnan, Georgia
  • Hackensack University Medical Center · Hackensack, New Jersey
  • Roswell Park Comprehensive Cancer Center · Buffalo, New York
  • Herbert Irving Comprehensive Cancer Center Columbia University Medical Center · New York, New York
  • Providence Portland Medical Center · Portland, Oregon

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See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06116786 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received targeted therapy and anti-PD-1 therapy.

Does this trial require EGFR?

Yes, EGFR wild-type is a required biomarker for enrollment.

Does this trial require ALK?

Yes, ALK wild-type is a required biomarker for enrollment.

Does this trial require ROS1?

Yes, ROS1 wild-type is a required biomarker for enrollment.

What disease stage is eligible?

Stage IIIB or IV is required.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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