Actively Recruiting

Phase 1
Age: 65Years +
All Genders
NCT05849207

Post-Transplant Cyclophosphamide in Patients Aged >/= 65 Years Undergoing Haploidentical Transplant

Led by Ronald Paquette · Updated on 2026-05-07

26

Participants Needed

1

Research Sites

244 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this phase 1 study is to determine the optimal dose of the immune suppressive drug, cyclophosphamide, following standard allogeneic stem cell transplant in patients aged \>/= 65 years with hematologic malignancies.

CONDITIONS

Official Title

Post-Transplant Cyclophosphamide in Patients Aged >/= 65 Years Undergoing Haploidentical Transplant

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient age �3E/= 65 years
  • Patient and related donor (if applicable) sign the informed consent form for the study
  • Patient meets standard criteria for allogeneic stem cell transplant
  • Patient is suitable to receive fludarabine and total body irradiation 800 cGy conditioning
  • Donor is willing to donate peripheral blood stem cells
Not Eligible

You will not qualify if you...

  • Diagnosis of myelofibrosis
  • High titer antibodies (>10,000 mean fluorescent intensity) against one or more donor HLA antigens
  • Prior autologous or allogeneic stem cell transplant
  • Requires sedation for cardiac MRI
  • Mechanical, magnetic, or electrically activated implants such as pacemakers, neurostimulators, or infusion pumps
  • Ferromagnetic implants or foreign bodies like intracranial clips, shrapnel, or metal chips
  • Claustrophobia, problems with enclosed spaces, or inability to lie flat

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cedars-Sinai Medical Center

Los Angeles, California, United States, 90048

Actively Recruiting

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Research Team

C

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CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

1

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