A Phase 2 Study of IPI-926 in Patients With Myelofibrosis

The purpose of this study is to determine the safety and efficacy of IPI-926 in patients with myelofibrosis (MF) (primary myelofibrosis [PMF], post-polycythemia vera myelofibrosis [post-PV MF], or post-essential thrombocythemia myelofibrosis [post-ET MF]).

Stanford is not currently accepting new patients for this trial. You may want to check clinicaltrials.gov to see if other locations are recruiting.

Investigator(s):

Intervention(s):

  • drug : IPI-926

Phase: Phase 2

Eligibility

Ages Eligible For Study:

18 Years - 90 Years

Inclusion Criteria

- ?18 years of age at the time of signing the ICF. - Voluntarily sign an ICF. - Pathologically confirmed PMF or post ET/PV MF as per the WHO diagnostic criteria (note that it must include at least Grade 1 marrow fibrosis, see Appendix 3) with intermediate-1, intermediate -2, or high risk disease according to the IWG prognostic scoring system (see Appendix 4). If patients have low risk disease, then they must have symptomatic splenomegaly that is ? 10 cm below left costal margin by physical exam. - ECOG performance of 0-2. - Life expectancy of at least 3 months. - Recovery to Grade 1 or baseline of any toxicities due to prior systemic treatments, excluding alopecia. - If a woman, be of non-child bearing potential or, for women of child-bearing potential (WCBP) (defined as a sexually mature woman who has not undergone surgical sterilization or who has not been naturally post-menopausal for at least 24 consecutive months for women ?55 years; for women >55 years 12 consecutive months), must have a negative serum or urine pregnancy test result within 2 weeks of first dose of study drug. - All WCBP and all sexually active male patients must agree to use adequate methods of birth control throughout the study. Adequate methods of contraception include use of oral contraceptives with an additional barrier method, double barrier methods (diaphragm with spermicidal gel or condoms with contraceptive foam), Depo-Provera, partner vasectomy, and total abstinence. - Ability to adhere to the study visit schedule and all protocol requirements.

External Links

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Contact information

Primary Contact:

Harshdeep Kaur 6507233589

Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

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