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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05535764
Study type Interventional
Source University of Utah
Contact Catherine Cromar
Phone 801-213-5652
Email catherine.cromar@hci.utah.edu
Status Recruiting
Phase Phase 1
Start date March 23, 2023
Completion date October 30, 2027

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