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OncoMatch/Clinical Trials/NCT07154290

A Study to Investigate Ubamatamab With and Without REGN7075 in Adult Participants With Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC)

Is NCT07154290 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Ubamatamab and REGN7075 for advanced/metastatic non-small cell lung cancer.

Phase 2RecruitingRegeneron PharmaceuticalsNCT07154290Data as of Jun 2026

Treatment: Ubamatamab · REGN7075 · SarilumabThis study will evaluate two study drugs called ubamatamab and REGN7075, to see if they can help treat advanced or metastatic Non-Small Cell Lung Cancer (NSCLC), and sarilumab, to evaluate to see if it can help with immune-related side effects from ubamatamab. The study is looking at: * How well ubamatamab and REGN7075 works * The side effects that ubamatamab and REGN7075 might cause * How much ubamatamab and REGN7075 is in the blood at different times * If the body makes antibodies to ubamatamab and/or REGN7075, this may cause the ubamatamab to not work as well

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Extracted eligibility criteria

Treatments studied

Other

UbamatamabREGN7075Sarilumab

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: MUC16 expression by IHC

tumor tissue (archival or fresh) available for testing MUC16 expression by immunohistochemistry inclusion (IHC)

Disease stage

Required: Stage IIIB, IIIC, IV

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 1 prior line

Must have received: standard of care treatment for advanced or metastatic NSCLC — first line

Has received appropriate first line standard of care treatment for advanced or metastatic NSCLC

Must have received: platinum-based chemotherapy

If platinum doublet chemotherapy was not administered as first line therapy, it is required in a later line of therapy prior to enrollment unless there is a documented reason why it is not appropriate

Cannot have received: anti-PD-1 therapy

Has progression of disease fewer than 84 days from starting initial anti-Programmed Cell Death (PD)-(L) 1 therapy

Cannot have received: anti-PD-1 therapy

Has received prior monoclonal antibody against PD-(L)1 within 21 days of the first dose of study intervention

Cannot have received: immunotherapy

Has had other prior anti-cancer immunotherapy within 21 days prior to study intervention

Cannot have received: cytotoxic chemotherapy

Has received prior cytotoxic chemotherapy within 21 days of the first dose of study intervention

Cannot have received: anti-EGFR antibody therapy

Has received an anti-EGFR antibody therapy within the following drug-specific window prior to first dose of study intervention (approximately 5 half-lives)

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

US trial sites

  • University of Tennessee Medical Center · Knoxville, Tennessee

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT07154290 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior anti-PD-1 therapy, anti-PD-1 therapy, immunotherapy disqualifies patients from enrollment.

Does this trial require MUC16?

Yes, MUC16 expression by IHC is a required biomarker for enrollment.

What disease stage is eligible?

Stage IIIB or IIIC 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.

Check if I qualify