drugset / Trial / NCT01909453

Study Comparing Combination of LGX818 Plus MEK162 Versus Vemurafenib and LGX818 Monotherapy in BRAF Mutant Melanoma

NCT01909453

Phase 3 Completed 921 enrolled Pfizer
RandomizedParallel-groupOpen-labelTreatment

Summary

This is 2-part, randomized, open label, multi-center, parallel group, phase III study comparing the efficacy and safety of LGX818 plus MEK162 to vemurafenib and LGX818 monotherapy in patients with locally advanced unresectable or metastatic melanoma with BRAF V600 mutation. A total of approximately 900 patients will be randomized. Part 1: Patients will be randomized in a 1:1:1 ratio to one of 3 treatment arms: 1. LGX818 450 mg QD plus MEK162 45 mg BID (denoted as Combo 450 arm) 2. LGX818 300 mg QD monotherapy (denoted as LGX818 arm) or 3. vemurafenib 960 mg BID (denoted as vemurafenib arm) Part 2: Patients will be randomized in a 3:1 ratio to one of the 2 treatment arms: 1. LGX818 300 mg QD plus MEK162 45 mg BID (denoted as Combo 300 arm) or 2. LGX818 300 mg QD monotherapy (denoted as LGX818 arm)

Timeline

Start
2013-09-12
Primary completion
2016-11-09
Completion
2024-09-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Binimetinib Small molecule 45 mg Oral
Subject Encorafenib Small molecule 300 mg Oral
Subject Encorafenib Small molecule 450 mg Oral
Comparator Vemurafenib Small molecule 960 mg Oral

Indications