Condition: Myelofibrosis · Sponsor: University of Utah
This is a single site, open-label, dose de-escalation, Phase 1 study of pegylated interferon alfa-2a administered after alloHCT in subjects with primary or secondary myelofibrosis. Part 1 of the study will assess the rate of dose-limiting toxicities (DLTs) during the DLT evaluation period and identify the Recommended Phase 2 Dose (RP2D). Once the RP2D is identified, 6 additional patients will be enrolled in the expansion cohort.
This description comes directly from the study's public registry record.
Rachel Kingsford · 801-585-0115 · Rachel.Kingsford@hci.utah.edu
Always discuss trial participation with your own doctor first.
| Huntsman Cancer Institute at the University of Utah | Salt Lake City, Utah, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05535764