drugset / Trial / NCT03669965

KRT-232 Compared to Ruxolitinib in Patients With Phlebotomy-Dependent Polycythemia Vera

NCT03669965

Phase 2 Unknown 20 enrolled Kartos Therapeutics, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This study evaluates KRT-232, a novel oral small molecule inhibitor of MDM2, for the treatment of patients with phlebotomy-dependent polycythemia vera (PV). Inhibition of MDM2 in PV is a new mechanism of action in PV. In Part A, patients must be resistant or intolerant to hydroxyurea or have undergone treatment with interferon. In Part B, patients must be resistant or intolerant to hydroxyurea. This study is a global, open-label Phase 2a/2b study to determine the efficacy and safety of KRT-232. In Part A of the study, patients will be randomly assigned to 5 arms with 2 different doses and 3 different dosing schedules of KRT 232. In Part B of the study, patients will be randomized either to treatment with KRT-232 administered at the recommended dose and schedule from Part A or to treatment with ruxolitinib.

Timeline

Start
2019-01-15
Primary completion
2022-04
Completion
2022-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Navtemadlin Small molecule 120 mg Oral
Subject Navtemadlin Small molecule 240 mg Oral
Comparator Ruxolitinib Small molecule