Haploidentical stem cell transplantation with early ATG and low-dose cyclophosphamide

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effects of early administration of anti-thymocyte globulin (ATG) and low-dose post-transplant cyclophosphamide in patients undergoing haploidentical hematopoietic stem cell transplantation (haplo-HCT). The research is conducted at Samsung Medical Center and aims to define optimal strategies for haplo-HCT in patients who lack a matched donor. By focusing on a single center, the study seeks to provide detailed insights into the outcomes associated with this specific treatment approach.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients undergoing haploidentical hematopoietic stem cell transplantation with ATG and low-dose post-transplant cyclophosphamide conditioning at the department of pediatrics, Samsung Medical Center.

Exclusion Criteria:

* A clinical trial subject (legal representative, if applicable) who do not consent or is unable to give written consent.

Where it's running

• Samsung Medical Center
  Seoul, South Korea Recruiting

Study contacts

• Principal investigator: Keon Hee Yoo, Professor — Samsung Medical Center
• Study coordinator: Hee Young Ju
• Email: hyju320@gmail.com
• Phone: 82-02-3410-0865

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.