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NCT Number: NCT06199427

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

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)

Recruiting

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Key information

Age range

0 month–21 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged ≥ 0 months and < 21 years
  • Patients diagnosed with NBS eligible for an allogeneic HSCT
  • Signed written informed consent signed by a parent or legal guardian

Exclusion criteria

Concomitant severe somatic disease associated with an additional risk of severe complications

Treatment and study plan

Cyclophosphamide

Drug

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

Ruxolitinib

Drug

Ruxolitinib 7 mg/m2 from day +5 after HSCT

Primary outcomes

  1. Event-free survival

    Time frame: 1 year after HSCT

    Events: graft failure, death

Secondary outcomes

  1. Overall survival

    Time frame: 1 year after HSCT

  2. Cumulative incidence of acute graft versus host disease

    Time frame: 1 year after HSCT

  3. Cumulative incidence of chronic graft versus host disease

    Time frame: 1 year after HSCT

  4. Cumulative incidence of engraftment

    Time frame: 100 days

  5. Cumulative incidence of graft failure

    Time frame: 1 year after HSCT

  6. Incidence of early organ toxicity

    Time frame: 100 days

  7. Cumulative incidence of transplant related mortality

    Time frame: 1 year after HSCT

  8. Cumulative incidence of viral infections

    Time frame: 1 year after HSCT

  9. Investigation of the concentration of ruxolitinib in the blood To investigate the pharmacokinetics of ruxolitinib

    Time frame: 1 month after HSCT

    The features of pharmacokinetics in children of different ages

Study contacts

Contact information is provided by the study sponsor or research team.

Alexandra Laberko, MD, PhD

CONTACT

[email protected]

74952876570

Dmitry Balashov, MD, PhD

CONTACT

[email protected]

+74956647091

Sponsors and collaborators

Lead sponsor

Federal Research Institute of Pediatric Hematology, Oncology and Immunology

Other

Registry information

Official study 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

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
Jan 10, 2024
Registry last updated
Jan 10, 2024

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.

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