Actively Recruiting

Age: 18Years +
All Genders
NCT03555851

Factors Affecting Post-transplant Cyclophosphamide (PTCy) Efficacy

Led by Wake Forest University Health Sciences · Updated on 2026-01-08

120

Participants Needed

1

Research Sites

889 weeks

Total Duration

On this page

Sponsors

W

Wake Forest University Health Sciences

Lead Sponsor

A

Atrium Health Levine Cancer Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will examine the influence of donor and recipient pharmacogenetics (PG), drug pharmacokinetics (PK), and T cell phenotypes and how it may permit a tailored dosing strategy to improve the therapeutic index of post-transplant cyclophosphamide (PTCy) and optimize the graft versus tumor effect, while minimizing acute and chronic graft versus host disease (GVHD).

CONDITIONS

Official Title

Factors Affecting Post-transplant Cyclophosphamide (PTCy) Efficacy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent and HIPAA authorization
  • Age 18 years or older at consent
  • Scheduled as recipient or donor for haplo-identical, matched related, or matched unrelated donor hematopoietic stem cell transplant with non-myeloablative regimen at Levine Cancer Institute
  • Recipient must have planned post-transplant cyclophosphamide
  • Ability to understand and comply with study procedures for entire study duration as determined by physician
Not Eligible

You will not qualify if you...

  • Recipient of haplo-identical or matched related transplant without a willing donor consenting to participate
  • Recipient treated with any investigational drug within 30 days before day -6 of treatment
  • Donor of haplo-identical or matched related transplant without a willing recipient consenting to participate

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

Levine Cancer Institute

Charlotte, North Carolina, United States, 28204

Actively Recruiting

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Research Team

E

Elizabeth Parke

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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