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 (May 2026). This Phase 2 trial studies multiple treatments including Ubamatamab and REGN7075 for advanced/metastatic non-small cell lung cancer.
Treatment: Ubamatamab · REGN7075 · Sarilumab — This 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
Check if I qualifyExtracted eligibility criteria
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
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
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