drugset / Trial / NCT01357655

Phase 2 Dasatinib Combo With Smoothened (SMO) Antagonist (BMS-833923)

NCT01357655 ↗

Phase 2 Terminated 70 enrolled Bristol-Myers Squibb
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to compare response rates in newly diagnosed Chronic Phase (CP) CML subjects treated with dasatinib plus BMS-833923 versus dasatinib alone.

Timeline

Start
2011-09
Primary completion
2016-01
Completion
2016-01

Outcome

Outcome not reported

Stopped (Enrollment): “No participants enrolled in this trial could receive the SMO antagonist as a recommended phase 2 dose was not determined by a different, concurrently-run trial.”

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-833923 Small molecule — Oral
Subject dasatinib anhydrous Small molecule 100 mg Oral

Indications