drugset / Trial / NCT02562443

Controlled Study of Rigosertib Versus Physician's Choice of Treatment in MDS Patients After Failure of an HMA

NCT02562443

Phase 3 Terminated 372 enrolled Traws Pharma, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The study's primary objective \[in a population of patients with MDS after failure of treatment with azacitidine (AZA) or decitabine (DAC)\], is to compare the overall survival (OS) of patients in the rigosertib group vs the Physician's Choice group, in all patients and in a subgroup of patients with IPSS-R very high risk.

Timeline

Start
2015-12-02
Primary completion
2020-07-26
Completion
2021-07-26

Drugs

EvaluationDrugModalityDoseRoute
Subject rigosertib Small molecule 1800 mg Intravenous
Background Azacitidine Other / unclassified
Background Decitabine Small molecule