Full Text View
Tabular View
No Study Results Posted
Related Studies
Bone Marrow Transplantation in Treating Children With Sickle Cell Disease
This study has been completed.
Study NCT00004485   Information provided by Office of Rare Diseases (ORD)
First Received: October 18, 1999   Last Updated: September 8, 2008   History of Changes

October 18, 1999
September 8, 2008
December 1999
August 2007   (final data collection date for primary outcome measure)
 
 
Complete list of historical versions of study NCT00004485 on ClinicalTrials.gov Archive Site
 
 
 
Bone Marrow Transplantation in Treating Children With Sickle Cell Disease
Phase I/II Study of Induction of Stable Mixed Chimerism After Bone Marrow Transplantation From HLA-Identical Donors in Children With Sickle Cell Disease

RATIONALE: Sickle cell disease is an inherited disorder in which abnormal, crescent-shaped red blood cells interfere with the ability of the blood to carry oxygen through the body and can cause severe pain, stroke, and organ damage. Bone marrow transplantation, is a procedure in which the soft, sponge-like tissue in the center of bones producing white blood cells, red blood cells, and platelets is replaced by bone marrow from a another person. Bone marrow transplantation may be an effective treatment in relieving the symptoms of sickle cell disease.

PURPOSE: Phase I/II trial to study the effectiveness of bone marrow transplantation in treating children who have sickle cell disease.

PROTOCOL OUTLINE: This is a multicenter study. Patients undergo total body irradiation on day 0, followed by allogeneic bone marrow transfusion. Patients also receive fludarabine IV daily and cyclosporine IV twice a day on days -1 to 1. Patients then receive oral cyclosporine on days 1-90, and oral mycophenolate mofetil twice a day on days 0-27.

Patients are followed for 100 days, monthly for 6 months and then annually for 2 years.

Phase I, Phase II
Interventional
Treatment
Sickle Cell Anemia
  • Drug: cyclosporine
  • Drug: fludarabine
  • Drug: mycophenolate mofetil
  • Procedure: Bone Marrow Transplantation
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
50
 
August 2007   (final data collection date for primary outcome measure)

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

Diagnosis of sickle cell anemia with clinically severe disease manifestations defined by: Recurrent painful events (at least 2 painful events in past year) which cannot be explained by other causes Pain lasts at least 4 hours Requires treatment with parenteral narcotics, equianalgesic dose of oral narcotics, or parenteral nonsteroidal antiinflammatory drugs Acute chest syndrome (ACS) with at least 2 episodes within past 2 years that required hospitalization, oxygen, and RBC transfusion Any combination of painful events and ACS episodes that total 2 events within the past year Abnormal cerebral MRI, abnormal angiography (MR or conventional), and abnormal neuropsychologic testing performance

No stage III or IV sickle cell lung disease

Genotypically HLA identical sibling donor available

--Prior/Concurrent Therapy--

No prior transfusions with greater than 5 units RBC

--Patient Characteristics--

Performance status: Karnofsky 70-100%

Hepatic:

  • No active hepatitis
  • No moderate/severe portal fibrosis

Renal: Glomerular filtration rate at least 30% predicted for age

Neurologic:

  • No severe residual functional neurologic impairment
  • Hemiplegia alone allowed

Other:

  • HIV negative
  • Not pregnant or nursing
  • Fertile patients must use effective contraception
Both
up to 16 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00004485
 
199/14243, FHCRC-1373.00
Fred Hutchinson Cancer Research Center
 
Study Chair: Mark Walters Children's Hospital of Oakland
Office of Rare Diseases (ORD)
September 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP