Drugs / Favezelimab

Trials 8

20162017201820192020202120222023202420252026202720282029203020312032203320342035203620372038203920402041204220432044
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Phase 1/2 NCT06395090 Jan 2025 → Jun 2029 metastatic neoplasm Merck Sharp & Dohme LLC Withdrawn No outcome recorded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 · 1 met primary
Phase 2 NCT03516981 Oct 2018 → Jun 2025 non-small cell lung carcinoma Merck Sharp & Dohme LLC Completed Met primary
Phase 2 NCT02625961 Feb 2016 → Nov 2025 urinary bladder cancer Merck Sharp & Dohme LLC Terminated No outcome recorded Stop: Business
Phase 32 trials · 1 missed
Phase 3 NCT05600309 Jun 2022 → Aug 2024 colorectal cancer Merck Sharp & Dohme LLC Completed Missed primary
Phase 3 NCT03486873 Aug 2018 → Aug 2043 expected cancer, hematopoietic and lymphoid cell neoplasm Merck Sharp & Dohme LLC Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2024-09-25 Merck Sharp & Dohme LLC Results Merck Provides Update on Phase 3 KEYFORM-007 Trial Evaluating Investigational Fixed-Dose Combination of Favezelimab and Pembrolizumab for Patients With Previously Treated PD-L1 Positive Microsatellite Stable Metastatic Colorectal Cancer merck.com ↗
At the final pre-specified analysis, the favezelimab and pembrolizumab fixed-dose combination did not demonstrate an improvement in OS compared to standard of care (regorafenib or TAS-102 [trifluridine and tipiracil hydrochloride]).

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 ↗

NCT06395090 ↗

NCT03598608 ↗

NCT04305054 ↗

NCT03516981 ↗

NCT02720068 ↗

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