HSCT department
Moscow, Russia
Location status: Recruiting
NCT Number: NCT06199427
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)
Interested in participating?
Request Info0 month–21 year
All sexes
Interventional
Phase 2
Moscow, Russia
Location status: Recruiting
Hematopoietic stem cell transplantation (HSCT) is widely used in inborn errors of immunity (IEI), and risks of graft-versus-host disease (GVHD) remain high. Use of post-transplant cyclophosphamide (PTCY) for GVHD prophylaxis revolutionized the outcomes of HSCT from mismatched related donor (MMRD). Use of ruxolitinib for GVHD prophylaxis demonstrates promising results in adult patients. Another well-known option for GVHD prevention is antithymocyte globulin. To evaluate the efficacy of combination of thymoglobulin with PTCY and ruxolitinib for GVHD prophylaxis, conditioning regimen containing treosulfan 30-42 g/m2, fludarabine 150 mg/mg, and thiotepa 10 mg/kg or melphalan 140 mg/m2 and GVHD prophylaxis regimen containing cyclophosphamide 50 mg/kg for MMRD, 25 mg/kg for matched unrelated and related donors at days +3, 4 post-HSCT and ruxolitinib at dose 7 mg/m2 from day +5 after HSCT will be used in patients with IEI.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Concomitant severe somatic disease associated with an additional risk of severe complications
Cyclophosphamide 25mg/kg (days +3, +4) after HSCT from MUD and MRD Cyclophosphamide 50mg/kg (days +3, +4) after HSCT from MMRD
Ruxolitinib 7 mg/m2 from day +5 after HSCT
Time frame: 1 year after HSCT
Events: graft failure, death
Time frame: 1 year after HSCT
Time frame: 1 year after HSCT
Time frame: 1 year after HSCT
Time frame: 100 days
Time frame: 1 year after HSCT
Time frame: 100 days
Time frame: 1 year after HSCT
Time frame: 1 year after HSCT
Time frame: 1 month after HSCT
The features of pharmacokinetics in children of different ages
Contact information is provided by the study sponsor or research team.
Alexandra Laberko, MD, PhD
CONTACT
Dmitry Balashov, MD, PhD
CONTACT
Federal Research Institute of Pediatric Hematology, Oncology and Immunology
Other
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06773546
Inborn Errors of Immunity
Bologna, Bolgona, Italy
View Trial DetailsNCT05803356
Immune System Diseases, Immunity Disorders
Trieste, Italy
View Trial Details