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Clinical Trial Summary

The purpose of this research is to gather information on the safety and effectiveness determining maximum tolerated dose (MTD) of ruxolitinib in combination with ivosidenib in IDH1-mutated advanced-phase Ph-negative MPNs while evaluate the efficacy of ruxolitinib in combination with ivosidenib in IDH1-mutated advanced-phase Ph-negative MPNs.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06291987
Study type Interventional
Source University of Chicago
Contact Clinical Trials Intake
Phone 1-855-702-8222
Email cancerclinicaltrials@bsd.uchicago.edu
Status Not yet recruiting
Phase Phase 1
Start date May 20, 2024
Completion date May 2026

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