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NCT07022457: UK-EnBiRiM

UK ENcorafenib and BInimetinib Real-world Study in Melanoma

Active, enrolled Last updated 13 April 2026
What this trial tests

trial testing Encorafenib + Binimetinib in Metastatic Melanoma, BRAF V600 Mutation Positive in 50 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
31 July 2025
Primary endpoint
13 January 2028
13 January 2028

Quick facts

Lead sponsorPierre Fabre Ltd
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment50
Start date31 July 2025
Primary completion13 January 2028
Estimated completion13 January 2028
Sites7 locations across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Pierre Fabre Ltd

Who can join

18 and older, any sex, with Metastatic Melanoma, BRAF V600 Mutation Positive. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective longitudinal multi-centre observational study conducted in the United Kingdom, in patients with metastatic cutaneous BRAF V600 mutation-positive melanoma assigned to receive encorafenib and binimetinib. The aim of this study is to learn about how encorafenib and binimetinib perform, patients' experiences of using them, and how they might affect patient's quality of life, in the real world, when these treatments are prescribed by doctors instead of in a clinical trial. Participants will complete electronic data entry via questionnaires over a 24-month period. Site research teams will also complete electronic data entry using participants' medical records over a 24-month period.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Encorafenib + Binimetinib

Trials testing the same drug.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07022457.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing