drugset / Trial / NCT02598297

Phase III Study Investigating the Efficacy and Safety of Ruxolitinib in Early Myelofibrosis Patients With High Molecular Risk Mutations.

NCT02598297

Phase 3 Terminated 49 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

Myelofibrosis patients with high molecular risk mutations have an intrinsically aggressive disease with increased risk of leukemic transformation and reduced overall survival. As there are no therapies currently established in the subset of high molecular risk patients with early myelofibrosis, the study aimed to evaluate ruxolitinib in this patient population.

Timeline

Start
2016-02-03
Primary completion
2017-10-23
Completion
2017-10-23

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ruxolitinib Small molecule 5 mg Oral

Indications