drugset / Trial / NCT01836705

Effect of SAR302503 on ECG Activity in Patients With Solid Tumors

NCT01836705

Phase 1 Completed 60 enrolled Bristol-Myers Squibb
Non-randomizedCrossoverOpen-labelBasic science

Summary

Primary Objective: \- To assess the effect of SAR302503 (500 mg) administered as 14-day repeated doses on the QTcF interval compared to 1-day placebo in patients with advanced solid tumors. Secondary Objectives: * To assess the effect of SAR302503 administered as 14-day repeated doses on heart rate (HR), QT, QTcB, and QTcN, PR and QRS compared to placebo. * To assess the clinical and laboratory safety of SAR302503 * To document the plasma concentrations of SAR302503 at the time of ECG investigation. * To explore the Pharmacokinetic/Pharmacodynamic relationship between SAR302503 concentration and QTcF * To explore antitumor activity

Timeline

Start
2013-05
Primary completion
2013-11
Completion
2014-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Fedratinib Small molecule 500 mg Oral
Background Panolosetron Unknown Intravenous

Indications