drugset / Trial / NCT01001299

A Pharmacokinetic Study of RO5185426 in Combination With a Drug Cocktail in Patients With Metastatic Melanoma

NCT01001299

Phase 1 Completed 25 enrolled Hoffmann-La Roche
Parallel-groupOpen-labelTreatment

Summary

This open-label single-arm study will evaluate the effect of RO5185426 \[RG7204; PLEXXIKON: PLX4032\] on the pharmacokinetics of five CYP450 substrates (caffeine, warfarin + vitamin K, omeprazole, dextromethorphan, midazolam) administered as a drug cocktail to patients with metastatic melanoma. The study will also evaluate efficacy and safety of RO5185426. On day 1, patients will receive the drug cocktail. On days 6 to 19, patients will receive RO5185426 twice daily. On day 20, patients will receive RO5185426 and the drug cocktail and on days 21 to 25, patients will receive RO5185426. Assessments will be made at regular intervals during the dosing periods and at follow-up. Patients may continue on study treatment (RO5185426) until the development of progressive disease or unacceptable toxicity. Target sample size \<50.

Timeline

Start
2009-11-30
Primary completion
2012-02-29
Completion
2012-02-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Caffeine Small molecule Oral
Subject Dextromethorphan Unknown Oral
Subject Midazolam Small molecule Oral
Subject Omeprazole Other / unclassified Oral
Subject Vemurafenib Small molecule 960 mg Oral
Subject Vitamin K Unknown Oral
Subject Warfarin Small molecule Oral

Indications