About this trial

This is a phase II, multicenter, open-label trial evaluating the safety and efficacy of pacritinib and selinexor in JAK inhibitor naïve patients with anemia and thrombocytopenia.

Eligibility criteria

Qualifiers

Adults ≥ 18 years of age capable of providing informed consent

Pathologically confirmed diagnosis of PMF, post-ET MF, or post-PV MF as per the World Health Organization (WHO) diagnostic criteria - Intermediate-1, Intermediate-2, or High-Risk disease by the Dynamic International Prognostic Scoring System (DIPSS)

Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2

Baseline splenomegaly ≥ 5cm palpable below the left costal margin and in the midclavicular line OR ≥ 450cc by imaging (i.e. ultrasound, CT, MRI)

Disqualifiers

Prior treatment with Janus kinase (JAK) inhibitors

Prior treatment with selinexor or other Exportin 1 (XPO1) inhibitors

Treatment with any MF-directed therapy (including investigational therapies and excluding hydroxyurea) within 2 weeks or 5.5 half-lives, whichever is shorter, of Cycle 1 Day 1

Completed hematopoietic cell transplant (HCT)

Trial design

Treatments tested in this trial

  • Pacritinib
  • Selinexor

Treatment groups

26 Participants
are divided into 1 treatment group

Locations

3
The University of Kansas Cancer Center-Westwood66205, WestwoodKansas, United States
Icahn School of Medicine at Mount Sinai10029, New YorkNew York, United States
Wake Forest Baptist Health Comprehensive Cancer Center27157, Winston-SalemNorth Carolina, United States

Sponsors and collaborators

John Mascarenhas

Lead sponsor

Icahn School of Medicine at Mount Sinai

Sponsor institution

Sobi, Inc.

Collaborator

Karyopharm Therapeutics Inc

Collaborator

National Cancer Institute (NCI)

Collaborator