drugset / Trial / NCT01815840

A Study of Two Vismodegib Regimens in Participants With Multiple Basal Cell Carcinomas

NCT01815840

Phase 2 Completed 229 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

This randomized, double-blind, regimen-controlled, phase II, multicenter study will assess the efficacy and safety of two different vismodegib regimens in participants with multiple basal cell carcinoma. Participants will receive vismodegib 150 mg orally once daily either in an intermittent schedule of 12 weeks vismodegib followed by 8 weeks placebo (Arm A) or as 24 weeks induction followed by an intermittent schedule of 8 weeks placebo followed by 8 weeks vismodegib (Arm B). Anticipated time on study treatment is 72 weeks.

Timeline

Start
2013-04-30
Primary completion
2015-08-27
Completion
2016-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Vismodegib Small molecule 150 mg Oral

Indications