A Trial to Learn How the Combination of Fianlimab With Cemiplimab and Chemotherapy Works Compared With Cemiplimab and Chemotherapy for Treating Adult Patients With Advanced Non-small Cell Lung Cancer
Part of paid clinical trials in Tucson, Arizona.
- Sponsor
- Regeneron Pharmaceuticals
- Study ID
- NCT05800015
- Phase
- PHASE2/PHASE3
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- fianlimab — DRUGAdministered intravenously (IV) every 3 weeks (Q3W)
- cemiplimab — DRUGAdministered IV Q3W
- Pemetrexed — DRUGIV Infusion, Q3W
- Paclitaxel — DRUGIV Infusion, Q3W
- Carboplatin — DRUGIV Infusion, Q3W
- Cisplatin — DRUGIV infusion, Q3W
- Placebo — DRUGIV infusion, Q3W
Study Details
This study is researching an investigational drug called fianlimab (also called REGN3767) with two other medications called cemiplimab and chemotherapy, individually called a "study drug" or collectively called "study drugs". 'Investigational' means that the study drug is not approved for use outside of this study by any Health Authority. Examples of chemotherapy drugs include the following: Paclitaxel plus carboplatin, and Pemetrexed plus cisplatin. The study is being conducted in patients who have advanced non-small cell lung cancer (NSCLC). The aim of the study is to see how effective the combination of fianlimab, cemiplimab, and chemotherapy is for treating advanced NSCLC, in comparison with cemiplimab and chemotherapy. The study is looking at several other research questions, including: * What side effects may happen from taking the study drugs * How much of each study drug is in your blood at different times * Whether the body makes antibodies against the study drugs (which could make the drug less effective or could lead to side effects) * How administering the study drugs might improve your quality of life
Key Dates
- Start date
- Aug 8, 2023
- Status verified
- Jan 2026
- Primary completion
- Jan 16, 2030
- Completion
- Dec 23, 2031
Study Design
- Enrollment
- 950 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Phase 2 - Arm ARandomized 1:1:1 fianlimab (higher dose) + cemiplimab + platinum-doublet chemotherapy
- Experimental: Phase 2 - Arm BRandomized 1:1:1 fianlimab (lower dose) + cemiplimab + platinum-doublet chemotherapy
- Experimental: Phase 2 - Arm CRandomized 1:1:1 cemiplimab + platinum-doublet chemotherapy + placebo
- Experimental: Phase 3 - Arm A or BRandomized 1:1 fianlimab (chosen dose) + cemiplimab + platinum-doublet chemotherapy
- Experimental: Phase 3 - Arm CRandomized 1:1 cemiplimab + platinum-doublet chemotherapy + placebo
Primary Outcome Measure
Objective response rate (ORR) as assessed by blinded independent review committee (BICR) using RECIST 1.1 [ Time Frame: Up to 136 Weeks ]
Locations (29)
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