drugset / Trial / NCT01844674

A Study on the Effect of Vemurafenib on the Pharmacokinetics of a Single Dose of Tizanidine in Patients With BRAFV600 Mutation-Positive Metastatic Malignancies

NCT01844674

Phase 1 Completed 18 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelOther

Summary

This open-label, multicenter, 3-period, fixed-sequence study will evaluate the effect of multiple oral doses of vemurafenib on the pharmacokinetics of a single oral dose of tizanidine in participants with BRAFV600 mutation-positive metastatic malignancies. Participants will receive a single oral dose of tizanidine on Day 1, vemurafenib orally twice daily on Days 2 to 21, and tizanidine and vemurafenib on Day 22. Eligible participants will have the option to continue treatment with vemurafenib as part of an extension study (NCT01739764).

Timeline

Start
2013-09-02
Primary completion
2014-08-26
Completion
2014-08-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Tizanidine Small molecule 2 mg Oral
Subject Vemurafenib Small molecule 960 mg Oral

Indications