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OpenTrials
Completed

NCT Number: NCT01141959

Blood Samples to Identify Biomarkers in Haploidentical Graft Recipients

The investigators are interested in identifying patient-specific factors related to donor chimerism in patients who receive nonmyeloablative hematopoietic stem cell transplants from haploidentical donors. We will look how patients' bodies break down and immediately respond to cyclophosphamide, fludarabine and mycophenolate mofetil.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Scheduled to receive nonmyeloablative conditioning which includes fludarabine
  • Scheduled to receive a haploidentical graft
  • Scheduled to receive postgrafting immunosuppression which includes oral mycophenolate mofetil (MMF) or enteric-coated mycophenolic acid
  • Age >18 years at the time of enrollment

Exclusion criteria

  • Diagnosed with an immunodeficiency disorder, including HIV

Treatment and study plan

Primary outcomes

  1. Donor T-cell chimerism

    Time frame: Day 28 post-transplant

Secondary outcomes

  1. Exposure to cyclophosphamide, fludarabine, and mycophenolate mofetil and their breakdown products

    Time frame: 1 week before through 3 weeks after transplant

Sponsors and collaborators

Lead sponsor

Fred Hutchinson Cancer Center

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Jun 11, 2010
Registry last updated
May 31, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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