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UnknownNCT04400045

Low Dose Treosulfan Based Conditioning Regimen in HSCT for Nijmegen Breakage Syndrome

Clinical Open-label Phase 2 Study of Low Dose Treosulfan Based Conditioning Regimen Efficacy in Hematopoietic Stem Cell Transplantation for Children With Nijmegen Breakage Syndrome

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
Federal Research Institute of Pediatric Hematology, Oncology and Immunology · Academic / Other
Sex
All
Age
3 Months – 21 Years
Healthy volunteers
Not accepted

Summary

The aim of the current study is to evaluate the safety and efficacy of low dose treosulfan based conditioning regimen in HSCT in Nijmegen breakage syndrome

Detailed description

Nijmegen breakage syndrome (NBS) is a DNA repair disorder. The only curative option for combine immunodeficiency in NBS is allogeneic hematopoietic stem cell transplantation (HSCT). Standard myeloablative conditioning regimens in DNA repair disorders lead to increased morbidity and mortality after HSCT. Low doses of alkylators are used to reduce toxicity rates, which, however, increase the risks of mixed chimerism and graft failure. The data of treosulfan usage in NBS are sparse. To evaluate the safety and efficacy of low dose treosulfan based conditioning regimen in NBS, treosulfan 21g/m2 in combination with fludarabine 150mg/mg, cyclophosphamide 40mg/kg, thymoglobulin (Genzyme) 5mg/kg and rituximab 100mg/m2 will be used from day -6 to -1 day, followed by stem cell infusion. The primary endpoint is event-free survival, where graft failure, death, and malignancies are considered as events.

Conditions

Interventions

TypeNameDescription
DRUGTreosulfanTreosulfan 21mg/m2 (days -6, -5, -4)

Timeline

Start date
2020-05-22
Primary completion
2023-05-01
Completion
2023-05-01
First posted
2020-05-22
Last updated
2020-06-25

Locations

1 site across 1 country: Russia

Source: ClinicalTrials.gov record NCT04400045. Inclusion in this directory is not an endorsement.