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Taking people in RussiaPhase 2/3

Tests drugs to prevent graft-versus-host disease after transplant in young blood cancer patients

Tests drugs to prevent graft-versus-host disease after transplant in young blood cancer patients.

Plain-language title generated from the registry record
Registry title: Preventing of GVHD with Post-transplantation Cyclophosphamide, Abatacept, Vedolizumab and Ruxolitinib At Children and Young Adults with Hemoblastosis

Key facts

Where
Moscow, RussiaSee the site
Phase
Phase 2/3

Where in Russia

  • National medical research center of pediatric haematology, oncology and immulogy named after Dmytriy RogachyovMoscow, RussiaTaking people

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
Federal Research Institute of Pediatric Hematology, Oncology and Immunology
Trial code
NCT06756152
Record updated
1 January 2025
Original description
GVHD prevention using a combination of post-transplantation cyclophosphamide in combination with abatacept, vedolizumab and Ruxolitinib in children and young adults with hematoloblastosis after myeloablative conditioning regimen with treosulfan/TBI, etoposide, fludarabine after HSCT from matched unrelated and haploidentical donorsRead full original descriptionShow less

Prospective Pilot Study of the Clinical Efficacy and Safety of the Method for Preventing a Graft-versus-host Disease Through the Agency of Using the Combination of Post-transplantation Cyclophosphamide with Abatacept, Vedolizumab and Ruxolitinib At Children and Young Adults with Hemoblastosis After Hematopoietic Stem Cell Transplantation from an Unrelated or Haploidentic Donor

GVHD prevention using a combination of post-transplantation cyclophosphamide in combination with abatacept, vedolizumab and Ruxolitinib in children and young adults with hematoloblastosis after myeloablative conditioning regimen with treosulfan/TBI, etoposide, fludarabine after HSCT from matched unrelated and haploidentical donors

Inclusion: Patients under the age of 21 years with following diseases:; acute lymphoblastic,; myeloblastic,; biphenotypic,; bilinear leukemia,; malignant lymphoma,; myelodysplastic syndrome,.

Exclusion: Uncontrolled viral, fungal or bacterial infection; Mental illness of the patient or caregivers, making it impossible to realize the essence of the study and compromising compliance with medical appointments and sanitary and hygienic regime 1 These patients may receive treatment according to the protocol, but the results will be evaluated separately; Clinical status:; Lansky/Karnowski index <70% (supplement No.1); Heart function: left ventricular ejection fraction <40% according to ultrasound of the heart1; Kidney function: clearance of endogenous creatinine < 70 ml / min; Liver function: total bilirubin, ALT, AST, ALP > 2 norms; Lung function: lung capacity <50%, for children who cannot carry out of respiratory function - oxygen saturation during pulse oximetry <92%; Age over 21 years; Patients with ALL outside clinical and hematological remission.

ClinicalTrials.gov NCT06756152