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NCT07249346 · ClinicalTrials.gov registry record · Phase 2

Dose-Expansion Study of Low Dose Post-Transplant Cyclophosphamide/Tacrolimus/Ruxolitinib for Graft-versus-Host Disease (GVHD) Prophylaxis in Myeloablative Allogeneic Peripheral Blood Stem Cell Transplantation

A Phase 2 study of Leukemia and Chronic Myelomonocytic Leukemia, sponsored by Hannah Choe, MD.

Recruiting
Registry status
Phase 2
Development phase
124
Enrollment target
1
Study location

NCT07249346 is a Phase 2 study of Leukemia and Chronic Myelomonocytic Leukemia that is actively recruiting participants, run by Hannah Choe, MD. The registered enrollment target is 124 participants, below the 486-participant average among 233 other Leukemia trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07249346, a Phase 2 study of Leukemia and Chronic Myelomonocytic Leukemia, is actively recruiting participants, sponsored by Hannah Choe, MD.

RECRUITING
Registry status
Phase 2
Development phase
124 participants
Enrollment target
1
Study location

Study Summary

This is an open label, non-randomized, multicenter, pilot, dose expansion study of low dose post-transplant cyclophosphamide (25 mg/kg on Days +3 and +4)/tacrolimus/ruxolitinib in the setting of myeloablative conditioning (MAC) allogeneic peripheral blood stem cell transplantation (PBSCT).

Interventions

  • DRUG Cyclophosphamide
  • DRUG Ruxolitinib
  • DRUG Tacrolimus
  • DRUG Myeloablative conditioning regimen
  • PROCEDURE Hematopoietic Stem Cell Transplantation

Study Locations (1)

Ohio

  • Ohio State University Comprehensive Cancer Center - Columbus

Trial Details

FieldValue
Enrollment Target 124 participants
Start Date 2026-06-01
Est. Completion 2027-06-01
Phase Phase 2

Sponsor

Hannah Choe, MD

2 total trials

What the Registry Record Tells You About NCT07249346

The ClinicalTrials.gov registry entry for NCT07249346 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 124 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 486-participant average among 233 other Leukemia trials with a reported enrollment target (74% lower). The listed sponsor is Hannah Choe, MD, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Leukemia appearing as the primary indexed condition, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT07249346 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT07249346 about?

NCT07249346 is a clinical study titled "Dose-Expansion Study of Low Dose Post-Transplant Cyclophosphamide/Tacrolimus/Ruxolitinib for Graft-versus-Host Disease (GVHD) Prophylaxis in Myeloablative Allogeneic Peripheral Blood Stem Cell Transplantation". This is an open label, non-randomized, multicenter, pilot, dose expansion study of low dose post-transplant cyclophosphamide (25 mg/kg on Days +3 and +4)/tacrolimus/ruxolitinib in the setting of myeloablative conditioning (MAC) allogeneic peripheral blood stem cell transplantation (PBSCT).

What is the current status of trial NCT07249346?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 124 participants. The study started on 2026-06-01. Estimated completion is 2027-06-01.

What conditions does trial NCT07249346 study?

This clinical trial studies the following conditions: Leukemia, Chronic Myelomonocytic Leukemia, Myelodysplasia.

What interventions are being tested in trial NCT07249346?

The interventions under investigation include: Cyclophosphamide (DRUG), Ruxolitinib (DRUG), Tacrolimus (DRUG), Myeloablative conditioning regimen (DRUG), Hematopoietic Stem Cell Transplantation (PROCEDURE).

Who is sponsoring clinical trial NCT07249346?

This trial is sponsored by Hannah Choe, MD, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07249346 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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