Bone Marrow Transplant From Related Donor for Patients With High Risk Hemoglobinopathies

NCT00040469 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2020-01-18

No results posted yet for this study

Summary

The major goal of this study is to determine the risks and benefits of bone marrow transplants in patients with severe thalassemia or sickle cell disease. Participation in this project will be for two years.

Conditions

Interventions

DRUG

Campath -1H

DRUG

Dilantin

DRUG

Busulfan

Sponsors & Collaborators

  • The Methodist Hospital Research Institute

    collaborator OTHER
  • Center for Cell and Gene Therapy, Baylor College of Medicine

    collaborator OTHER
  • Baylor College of Medicine

    lead OTHER

Principal Investigators

  • Malcolm K. Brenner, MD · Baylor College of Medicine

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
1 Day
Max Age
64 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-08-31
Primary Completion
2003-11-21
Completion
2003-11-21

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00040469 on ClinicalTrials.gov