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NCT02861417 · ClinicalTrials.gov registry record · Phase 2

Busulfan, Fludarabine Phosphate, and Post-Transplant Cyclophosphamide in Treating Patients With Blood Cancer Undergoing Donor Stem Cell Transplant

A Phase 2 study of Myelodysplastic Syndrome and Hematopoietic and Lymphoid Cell Neoplasm, sponsored by M.D. Anderson Cancer Center.

Active
Registry status
Phase 2
Development phase
204
Enrollment target
1
Study location

NCT02861417: Active Phase 2 study of Myelodysplastic Syndrome and Hematopoietic and Lymphoid Cell Neoplasm, sponsored by M.D. Anderson Cancer Center.

NCT02861417 is a Phase 2 study of Myelodysplastic Syndrome and Hematopoietic and Lymphoid Cell Neoplasm that is active but no longer recruiting, run by M.D. Anderson Cancer Center. The registered enrollment target is 204 participants, roughly in line with the 206-participant average among 134 other Myelodysplastic Syndrome trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02861417, a Phase 2 study of Myelodysplastic Syndrome and Hematopoietic and Lymphoid Cell Neoplasm, is active but no longer recruiting, sponsored by M.D. Anderson Cancer Center.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
204 participants
Enrollment target
1
Study location

Study Summary

This phase II trial studies the side effect of busulfan, fludarabine phosphate, and post-transplant cyclophosphamide in treating patients with blood cancer undergoing donor stem cell transplant. Drugs used in chemotherapy, such as busulfan, fludarabine phosphate and cyclophosphamide work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving chemotherapy such as busulfan and fludarabine phosphate before a donor stem cell transplant helps stop the growth of cells in the bone marrow, including normal blood-forming cells (stem cells) and cancer cells. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells (called graft-versus-host disease). Giving cyclophosphamide after the transplant may stop this from happening. Once the donated stem cells begin working, the patient's immune system may see the remaining cancer cells as not belonging in the patient's body and destroy them.

Primary Outcome

The proportion of patients with non-relapse mortality will be reported separately by arm, along with the corresponding 95% Bayesian credible interval.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • DRUG Busulfan
  • DRUG Fludarabine Phosphate
  • PROCEDURE Allogeneic Hematopoietic Stem Cell Transplantation

Study Locations (1)

Texas

  • M D Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 204 participants
Start Date 2016-08-05
Est. Completion 2026-08-31
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the registry record for NCT02861417 still lists

NCT02861417 is an interventional study that assigns participants to a tested intervention. The registered 204 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 206-participant average among 134 other Myelodysplastic Syndrome trials with a reported enrollment target.

The record links to 10 conditions, with Myelodysplastic Syndrome appearing as the primary indexed condition, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT02861417 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT02861417 about?

NCT02861417 is a clinical study titled "Busulfan, Fludarabine Phosphate, and Post-Transplant Cyclophosphamide in Treating Patients With Blood Cancer Undergoing Donor Stem Cell Transplant". This phase II trial studies the side effect of busulfan, fludarabine phosphate, and post-transplant cyclophosphamide in treating patients with blood cancer undergoing donor stem cell transplant. Drugs used in chemotherapy, such as busulfan, fludarabine phosphate and cyclophosphamide work in differen...

What is the current status of trial NCT02861417?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 204 participants. The study started on 2016-08-05. Estimated completion is 2026-08-31.

What conditions does trial NCT02861417 study?

This clinical trial studies the following conditions: Myelodysplastic Syndrome, Hematopoietic and Lymphoid Cell Neoplasm, Recurrent Acute Myeloid Leukemia, Recurrent Acute Lymphoblastic Leukemia, Myelodysplastic/Myeloproliferative Neoplasm.

What interventions are being tested in trial NCT02861417?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), Busulfan (DRUG), Fludarabine Phosphate (DRUG), Allogeneic Hematopoietic Stem Cell Transplantation (PROCEDURE).

Who is sponsoring clinical trial NCT02861417?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02861417 being conducted?

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

Similar trials for Myelodysplastic Syndrome

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02861417's enrollment target sits among peer trials

204 18th of 134 higher than 117 of 134 other Myelodysplastic Syndrome trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Myelodysplastic Syndrome trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02861417, the US trial registry maintained by the National Library of Medicine. NCT02861417 (mid enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.