RecruitingPhase 1Phase 2NCT07128381

Phase I/II Clinical Trial of Axatilimab, a CSF1R Monoclonal Antibody, in Combination With Ruxolitinib as Therapy for Patients With Myelofibrosis (MF) and Chronic Myelomonocytic Leukemia (CMML)


Sponsor

M.D. Anderson Cancer Center

Enrollment

66 participants

Start Date

Jan 2, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

* To find the recommended dose of axatilimab given alone and in combination with ruxolitinib in patients with MF and CMML. * To learn if axatilimab given in combination with ruxolitinib can help to control MF and CMML.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of two targeted drugs — axatilimab (which targets a protein called CSF1R) and ruxolitinib (a JAK inhibitor) — in people with myelofibrosis or chronic myelomonocytic leukemia (CMML), two types of blood cancers. **You may be eligible if...** - You are 18 or older - You have been diagnosed with myelofibrosis (MF) or CMML - For MF: you have had at least one prior MF therapy, or have had a suboptimal response to a JAK inhibitor for at least 3 months, or have newly diagnosed intermediate-risk MF - For CMML: your disease did not respond to hydroxyurea or you have tried at least 4 cycles of a hypomethylating agent **You may NOT be eligible if...** - Your disease has progressed to acute leukemia - You have active serious infections or uncontrolled other illnesses - You have significant heart problems - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

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

DRUGAxatilimab (SNDX-6352)

Taken orally

DRUGRuxolitinib

Taken orally


Locations(1)

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07128381


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