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NotablePrimary and study completion dates: May 31, 2023 to Jan 6, 2025Trial status: Recruiting to Active, Not Recruiting · Site details revised at 42 of 42 sitesv19Show 2 more changesShow less
Trial status: Recruiting to Active, Not Recruiting
Site details revised at 42 of 42 sites
MinorStudy sites: 40 to 42v18
MinorStudy sites: 34 to 40v17
MinorStudy sites: 30 to 34v16
MinorStudy sites: 27 to 30v15
MinorStudy sites: 25 to 27v14
MinorStudy sites: 23 to 25v13
MinorStudy sites: 15 to 23Eligibility criteria expanded, about 63 wordsv12Show 1 more changeShow less
NotableTrial status: Not Yet Recruiting to RecruitingStudy sites: 0 to 1 · Start date changed from estimate of Apr 2021 to Mar 17, 2021v4Show 2 more changesShow less
Study sites: 0 to 1
Start date changed from estimate of Apr 2021 to Mar 17, 2021
MinorEnrollment target: 138 to 112Start date: Mar 2021 to Apr 2021 · Eligibility criteria expanded, about 66 words · Secondary endpoints revised (11) · 1 morev3Show 4 more changesShow less
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a Phase 2, multicenter, two-arm, open-label study to evaluate the safety and efficacy of selinexor versus treatment per physician's choice (PC) in participants with myelofibrosis (MF) who had at least 6 months of treatment with a Janus kinase (JAK)1/2 inhibitor. Study participants will be randomized in a 1:1 ratio to either receive selinexor or physicians' choice of treatment.