A Trial to Learn if Fianlimab and Cemiplimab Are Safe and Work Better Than Anti-PD1 Alone in Adult Participants With Resectable Stage 3 or 4 Melanoma

StatusActive, Not Recruiting
PhasePhase 2
Started

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Record History

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  1. Minor Trial status: Recruiting to Active, Not Recruitingv15 Show 4 more changesShow less
    • Enrollment target: estimated 150 to confirmed 151
    • Primary completion date: Mar 11, 2027 to Nov 2, 2026
    • Study completion date: Apr 23, 2031 to Dec 9, 2030
    • Site details revised at 104 of 104 sites
  2. Minor Study sites: 54 to 104v14
  3. Minor Study sites revised (54)v13
  4. Minor Site details revised at 1 of 54 sitesv12
  5. Minor Site details revised at 1 of 54 sitesv11
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  1. Minor Study sites: 52 to 54v10
  2. Minor Study sites: 50 to 52v9
  3. Minor Study sites: 45 to 50v8
  4. Notable Phase: Phase 2/3 to Phase 2v7 Show 9 more changesShow less
    • Enrollment target: 520 to 150
    • Primary completion date: Sep 21, 2028 to Mar 11, 2027
    • Primary endpoints: 2 to 1
    • Study sites: 31 to 45
    • Study completion date: Jun 4, 2033 to Apr 23, 2031
    • Interventions: cemiplimab (Drug), cemiplimab+fianlimab (Drug), fianlimab (Drug), pembrolizumab (Drug) to Fixed Dose Combination (FDC) cemiplimab+fianlimab (Drug), Placebo (Drug), cemiplimab (Drug)
    • Eligibility criteria revised
    • Secondary endpoints: 26 to 25
    • Study arms: 4 to 3
  5. Minor Study sites: 25 to 31v6
  6. Minor Study sites: 13 to 25v5
  7. Minor Study sites: 10 to 13v4
  8. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 10
    • Start date changed from estimate of Jul 12, 2024 to Sep 18, 2024
    v3
  9. Notable Phase: Phase 2 to Phase 2/3v2 Show 10 more changesShow less
    • Primary completion date: Dec 23, 2030 to Sep 21, 2028
    • Start date: Feb 9, 2024 to Jul 12, 2024
    • Primary endpoints: 1 to 2
    • Enrollment target: 360 to 520
    • Study completion date: Dec 23, 2030 to Jun 4, 2033
    • Interventions: Placebo (Drug), cemiplimab (Drug), fianlimab HD (Drug), fianlimab LD (Drug), pembrolizumab (Drug) to cemiplimab (Drug), cemiplimab+fianlimab (Drug), fianlimab (Drug), pembrolizumab (Drug)
    • Eligibility criteria shortened, about 23 words
    • Secondary endpoints: 24 to 26
    • Study arms: 3 to 4
    • Study title expanded, about 1 word
  1. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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This study is researching an experimental drug called REGN3767, also known as fianlimab (R3767), when combined with another medication called cemiplimab (each individually called a "study drug" or called "study drugs" when combined) compared with cemiplimab alone. These types of immunotherapy study drugs are collectively known as immune checkpoint inhibitors. Immunotherapies are treatments that use the immune system to recognize and kill cancer cells. The study is focused on participants with a type of skin cancer known as melanoma. The objective of this study is to see if the combination of fianlimab and cemiplimab is an effective treatment compared to cemiplimab in participants with high-risk, resectable melanoma. Participants will receive treatment before surgery, undergo resection, and then will have the option to continue treatment after resection. The study is looking at several other research questions, including: * What side effects may happen from receiving the study drug(s). * How much study drug(s) is in the blood at different times. * Whether the body makes antibodies against the study drug(s) (which could make the drug less effective or could lead to side effects). Antibodies are proteins that are naturally found in the blood stream that fight infections. * How administering the study drugs might improve quality of life.
Trial Details
NCT Number NCT06190951
Lead Sponsor Regeneron Pharmaceuticals
Conditions
(from sponsor)
Melanoma
Related terms Melanoma, Skin Neoplasms
Enrollment 151 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov