Completed

Stem Cell Transplantation for Genetic Diseases Treatment

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Study Aim

This study aims to treat genetic diseases by transplanting stem cells.

What is being tested

Stem Cell Transplantation

Procedure
Who is being recruted

Bone Marrow Failure Disorders+42

+ Congenital Bone Marrow Failure Syndromes

+ Cytopenia

Until 17 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: January 1995
See protocol details

Summary

Principal SponsorNational Center for Research Resources (NCRR)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Study start date: January 1, 1995

Actual date on which the first participant was enrolled.

PROTOCOL OUTLINE: Patients receive either cyclophosphamide and high dose total body irradiation (TBI) or busulfan and cyclophosphamide. Cyclophosphamide IV is given on days -5 and -4 and TBI on days -2, -1, and 0. Busulfan is given orally every 6 hours on days -9 through -6 and cyclophosphamide IV on days -5 through -2. Patients rest on day -1. Patients receive bone marrow infusion on day 0. For GVHD prophylaxis, patients receive methotrexate on day 1, then on days 3, 6, and 11. Cyclosporine IV begins on day -2 over 12 hours, followed by continuous infusion for 21 days. Then, oral doses of cyclosporine are given every 12 hours to patients who tolerate oral feeding. Cyclosporine is continued 6 months posttransplant, then tapered 10% per week and stopped. Patients who receive genotypically HLA nonidentical stem cells undergo additional GVHD prophylaxis with methylprednisolone (IV or PO) or its equivalent every 12 hours on days 3 to day 100. Dose is then tapered as tolerated over 1 month. Patients who receive cord blood stem cells receive methylprednisolone instead of methotrexate for GHVD prophylaxis. Methylprednisolone is given 3 times daily beginning on day 5 and continuing until day 17. Then, methylprednisolone is tapered 10% per week as clinically tolerated. To accelerate engraftment, patients receive filgrastim IM daily beginning on day +1 and continuing until ANC equals 5000.

NCT00004378
Principal SponsorNational Center for Research Resources (NCRR)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Until 17 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Bone Marrow Failure DisordersCongenital Bone Marrow Failure SyndromesCytopeniaAnemiaAnemia, HemolyticAnemia, Hemolytic, CongenitalBlood Platelet DisordersBone Marrow DiseasesBrain DiseasesBrain Diseases, MetabolicCentral Nervous System DiseasesDemyelinating DiseasesHemic and Lymphatic DiseasesHemoglobinopathiesLipid Metabolism, Inborn ErrorsLipidosesMetabolic DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesNervous System DiseasesNutritional and Metabolic DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsThalassemiaLysosomal Storage DiseasesLysosomal Storage Diseases, Nervous SystemHereditary Central Nervous System Demyelinating DiseasesBrain Diseases, Metabolic, InbornDisease AttributesAnemia, Hypoplastic, CongenitalDNA Repair-Deficiency DisordersLipid Metabolism DisordersSulfatidosisLeukoencephalopathiesAnemia, AplasticFanconi AnemiaHematologic DiseasesLeukodystrophy, MetachromaticMetabolism, Inborn ErrorsRed-Cell Aplasia, PureSphingolipidosesThrombocytopeniabeta-ThalassemiaAnemia, Diamond-BlackfanGenetic Diseases, InbornRare Diseases

Criteria

PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Hereditary enzymopathies, such as: Metachromatic leukodystrophy Congenital Immunodeficiencies Heritable hematologic disorders, such as: Thalassemia major Refractory Diamond-Blackfan anemia Fanconi anemia Amegakaryocytic thrombocytopenia --Patient Characteristics-- Age: Under 18 Other: SCT is performed using a histocompatible related donor, an unrelated donor, or an unrelated cord blood donor Haploidentical donors are accepted for patients with severe congenital immunodeficiency

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

University of California Los Angeles Medical Center

Los Angeles, United StatesOpen University of California Los Angeles Medical Center in Google Maps
CompletedOne Study Center