Effectiveness and Safety of a Single-Center Clinical Study on a CD25 Monoclonal Antibody-Containing GVHD Prophylaxis Scheme to Reduce the Incidence of Severe Acute GVHD After Umbilical Cord Blood Transplantation for Malignant Hematologic Diseases

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorAnhui Provincial Hospital

About this trial

Evaluating the safety and effectiveness of a CD25 monoclonal antibody-based prophylactic acute graft-versus-host-disease (aGVHD) regimen following unrelated umbilical cord blood transplantation (UCBT) for malignant hematologic disorders in reducing severe aGVHD.

Eligibility criteria

Qualifiers

Malignant hematologic disorders;

Patients undergoing UCBT;

Female patients of childbearing potential must have a negative pregnancy test and agree to use effective contraception during treatment and for the following year.

Disqualifiers

Non-malignant hematologic disorders;

History of allogeneic hematopoietic stem cell transplantation or solid organ transplantation;

Uncontrolled bacterial, viral, or fungal infections. "Uncontrolled" is defined as lack of clinical improvement or progression despite adequate antimicrobial therapy;

HIV infection or active hepatitis B or C virus infection;

Trial design

Treatments tested in this trial

  • Basiliximab

Treatment groups

39 Participants
are divided into 1 treatment group

Sponsors and collaborators