Brief Summary
This study evaluates KRT-232, a novel oral small molecule inhibitor of MDM2, for the treatment of patients with myelofibrosis (MF) who no longer benefit from treatment with a JAK inhibitor. Inhibition of MDM2 is a novel mechanism of action in MF.
This study will be conducted in 2 phases. Phase 2 will determine the KRT-232 recommended dosethe amount of medication taken and dosing schedule; Phase 3 will test KRT-232 vs Best Available Therapy (BAT). Patients in the Phase 3 part of the study will be randomized 2:1 to receive either KRT-232 (Arm 1) or BAT (Arm 2). The BAT administered will be determined by the treating physician, with the option to “cross-over” to KRT-232 treatment after 6 months of BAT or if the disease worsens at any time.
Intervention / Treatment
- Drug: KRT-232
- Drug: Best Available Therapy (BAT)
Inclusion Criteria
- Confirmed diagnosisthe process of identifying a disease based on signs and symptoms, patient history and medical test results of PMF, post-PV MF or post-ET MF (WHO)
- High, intermediate-2, or intermediate-1 riskthe possibility that something bad will happen Dynamic International Prognostic System (DIPSS)
- Failure of prior treatment with JAK inhibitor
- ECOG ≤ 2