RecruitingPhase 1NCT06291987

Ivosidenib and Ruxolitinib in Patients With Advanced Myeloproliferative Neoplasms (MPNs) That Have an IDH1 Gene Mutation

A Phase 1b Trial of Ivosidenib Combined With Ruxolitinib in IDH1-Mutated Advanced-Phase MPNs


Sponsor

University of Chicago

Enrollment

18 participants

Start Date

Sep 19, 2024

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Ivosidenib and a drug called Ruxolitinib for people with myeloproliferative neoplasms. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGIvosidenib

Ivosidenib will be given at assigned dose once daily.

DRUGRuxolitinib

Ruxolitinib will be given at assigned dose twice daily.


Locations(2)

University of Chicago Medicine Comprehensive Cancer Center

Chicago, Illinois, United States

Froedtert Hospital & the Medical College of Wisconsin

Milwaukee, Wisconsin, United States

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NCT06291987


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