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RECRUITING
NCT06199427
PHASE2

PTCy and and Ruxolitinib for GVHD Prophylaxis After HSCT With Thymoglobulin in Conditioning Regimen in Patients With Inborn Errors of Immunity

Sponsor: Federal Research Institute of Pediatric Hematology, Oncology and Immunology

View on ClinicalTrials.gov

Summary

The aim of the current study is to evaluate the efficacy of combined regimen of GVHD prophylaxis with thymoglobulin in conditioning regimen and PTCY with ruxolitinib used after HSCT in patients with inborn errors of immunity (IEI)

Official title: Safety and Efficacy of Cyclophosphamide and Ruxolitinib for Graft-versus-host-disease Prophylaxis After Hematopoietic Stem Cell Transplantation With Thymoglobulin Serotherapy in Conditioning Regimen in Patients With Inborn Errors of Immunity

Key Details

Gender

All

Age Range

0 Months - 21 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2023-11-21

Completion Date

2027-12-31

Last Updated

2024-01-10

Healthy Volunteers

No

Interventions

DRUG

Cyclophosphamide

Cyclophosphamide 25mg/kg (days +3, +4) after HSCT from MUD and MRD Cyclophosphamide 50mg/kg (days +3, +4) after HSCT from MMRD

DRUG

Ruxolitinib

Ruxolitinib 7 mg/m2 from day +5 after HSCT

Locations (1)

HSCT department

Moscow, Russia