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Post-transplantation Cyclophosphamide for Haploidentical Transplant From Maternal or Collateral Donors

P

Peking University

Status and phase

Completed
Phase 4

Conditions

Hematopoietic Stem Cell Transplantation

Treatments

Drug: post-transplantation cyclophosphamide

Study type

Interventional

Funder types

Other

Identifiers

NCT02412423
2015PHB016-01

Details and patient eligibility

About

In "beijing model" for haploidentical transplant, the rate of acute graft-versus-host disease (GVHD) from maternal or collateral donors was significantly higher than that from other kins. To reduce the GVHD incidence from maternal or collateral donors, post-transplantation cyclophosphamide is planned to be added into the protocol in "beijing model".

Enrollment

30 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • haploidentical patients from maternal or collateral donors

Exclusion criteria

  • uncontrolled infection before transplant

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

treatment group
Experimental group
Description:
post-transplantation cyclophosphamide
Treatment:
Drug: post-transplantation cyclophosphamide

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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