Graft Versus Host Disease (GvHD) Clinical Trials

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Application of Thymoglobulin (ATG) Individualized Dosing Model in Unrelated Allogeneic Hematopoietic Stem Cell Transplantation.

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Anti-thymocyte globulin (ATG) is widely used in allogeneic hematopoietic stem cell transplantation to prevent severe graft-versus-host disease (GVHD) and graft failure. However, overexposure to ATG may increase cytomegalovirus (CMV), Epstein-Barr virus (EBV) reactivation, non-relapse mortality, and disease recurrence. A targeted dosing strategy was established based on ATG concentration monitoring and conducted a phase 2 trial to evaluate the safety and efficacy of the dosing strategy in adult unmanipulated haplo-PBSCT, a encouraging result was attained. In this trial, The ATG-targeted dosing strategy was extended to adult unrelated donor allogeneic hematopoietic stem cell transplantation, ATG was administered for 4 days (-5 days to -2 days) during conditioning. The ATG doses on-3 days and- 2days were adjusted by our dosing strategy to achieve the optimal ATG exposure. The primary endpoint was CMV reactivation on +180 days.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 14
Maximum Age: 65
Healthy Volunteers: f
View:

• Patients with malignant hematological tumors who have indications for allogeneic hematopoietic stem cell transplantation.

• HLA-matched unrelated donor

• Patient age ≥14 years old and ≤65 years old

• ALT and AST ≤ 2.5 times the upper limit of normal values, bilirubin ≤ 2 times the upper limit of normal values

• Creatinine ≤ high limit of normal value

• No uncontrollable infection or serious mental illness

• Physical strength score is 0-2 (ECOG)

• Sign the informed consent form

Locations
Other Locations
China
Department of Hematology, First Medical Center of Chinese PLA General Hospital
RECRUITING
Beijing
Contact Information
Primary
Sheng Chen, master
csto301@163.com
15101156205
Time Frame
Start Date: 2020-12-31
Estimated Completion Date: 2025-06-30
Participants
Target number of participants: 30
Treatments
Experimental: targeted dosing ATG cohort
The targeted dosing ATG cohort received the same dose of medication at -5 days and -4 days as the traditional administration method (-5days, 1.5mg/kg; -4days 2.5mg/kg), Two individual doses were given on -3days and day -2days according to the dose adjustment strategy.
Sponsors
Leads: Chinese PLA General Hospital

This content was sourced from clinicaltrials.gov