Drugs / Favezelimab

Trials 8 · a red edge is where a trial was stopped

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PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT02720068 May 2016 → Mar 2024 neoplasm Merck Sharp & Dohme LLC Completed No outcome recorded
Phase 1/23 trials
Phase 1/2 NCT06395090 Jan 2025 → Jun 2029 metastatic neoplasm Merck Sharp & Dohme LLC Withdrawn No outcome recorded
Phase 1/2 NCT04305054 Jul 2020 → May 2026 melanoma Merck Sharp & Dohme LLC Completed No outcome recorded
Phase 1/2 NCT03598608 Oct 2018 → Jan 2026 classic Hodgkin lymphoma, large B-cell lymphoma, non-Hodgkin lymphoma Merck Sharp & Dohme LLC Completed No outcome recorded
Phase 22 trials
Phase 2 NCT03516981 Oct 2018 → Jun 2025 non-small cell lung carcinoma Merck Sharp & Dohme LLC Completed No outcome recorded
Phase 2 NCT02625961 Feb 2016 → Nov 2025 urinary bladder cancer Merck Sharp & Dohme LLC Completed No outcome recorded
Phase 32 trials
Phase 3 NCT05600309 Jun 2022 → Aug 2024 colorectal cancer Merck Sharp & Dohme LLC Completed No outcome recorded
Phase 3 NCT03486873 Aug 2018 → Aug 2043 expected cancer, hematopoietic and lymphoid cell neoplasm Merck Sharp & Dohme LLC Recruiting No outcome recorded

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 10 sources stand behind the page.

FieldValueCited text
Known as favezelimab “Participants receive MK-4280A (800mg favezelimab + 200mg pembrolizumab) as IV infusion every 3 weeks (Q3W) and may continue study therapy until study treatment completion or...” NCT03486873
6

NCT05600309

NCT02720068

NCT04305054

NCT03516981

NCT06395090

NCT03598608

Known as Favezelimab/pembrolizumab coformulation ClinicalTrials.gov intervention name — accepted as the source's own label NCT02625961
Action Inhibit “anti-LAG-3 favezelimab” PMID 37429923 Jul 2023
Route Intravenous “receive favezelimab/pembrolizumab (coformulation of 800mg favezelimab and 200 mg pembrolizumab) via IV infusion” NCT02625961
Target LAG3 “LAG-3 antibody favezelimab” PMID 36493599 Dec 2022