drugset / Trial / NCT01072175

Investigate Safety, Pharmacokinetics and Pharmacodynamics of GSK2118436 & GSK1120212

NCT01072175 ↗

Phase 2 Completed 430 enrolled Novartis Pharmaceuticals
Non-randomizedOpen-labelTreatment

Summary

This was an open-label, dose escalation study to investigate the safety, pharmacokinetics, pharmacodynamics and clinical activity of GSK2118436 and GSK1120212 in combination. This study was designed in four parts. In Part A, the effect of repeat doses of GSK1120212 on the pharmacokinetics of single dose GSK2118436 was investigated prior to evaluating combination regimens. In Part B, the range of tolerated dose combinations was identified using a dose-escalation procedure. In Part C, different dose combinations of GSK2118436 and GSK1120212 were evaluated, based on results from the dose escalation cohorts. In Part D, the pharmacokinetics and safety of GSK2118436 administered as HPMC capsules alone and in combination with GSK1120212 was evaluated.

Timeline

Start
2010-03-26
Primary completion
2012-05-31
Completion
2018-02-27

Outcome

Mixed primary results

registry analysis (superiority or other test); Part C: Dabrafenib 150 mg vs Part C: Dabrafenib 150 mg + Trametinib 1 mg; p = 0.0048; Hazard Ratio (HR) 0.58 (95% CI 0.38 to 0.87); Log Rank NCT01072175 ↗

registry analysis (superiority or other test); Part C: Dabrafenib 150 mg vs Part C: Dabrafenib 150 mg + Trametinib 1 mg; p = 0.1667; Hazard Ratio (HR) 0.73 (95% CI 0.45 to 1.18); Log Rank NCT01072175 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dabrafenib Small molecule 75 mg —
Subject Dabrafenib Small molecule 150 mg —
Subject Dabrafenib Small molecule 300 mg —
Subject Trametinib Small molecule 1 mg —
Subject Trametinib Small molecule 2 mg —
Subject Trametinib Small molecule 3 mg —

Indications