Study of Total Body Irradiation and Fludarabine Followed By Allogeneic Peripheral Blood Stem Cell or Bone Marrow Transplantation in Combination With Cyclosporine and Mycophenolate Mofetil in Patients With Inherited Disorders

Metabolism, Inborn Errors Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00010361
• Other study ID #: 199/15577
• Secondary ID: FHCRC-1475.00
• Status: Completed
• Phase: N/A
• First received: February 2, 2001
• Last updated: December 8, 2014
• Start date: November 2000

Study information

• Verified date: August 2006
• Source: Office of Rare Diseases (ORD)
• Contact: n/a
• Is FDA regulated: No
• Health authority: Unspecified
• Study type: Interventional

Clinical Trial Summary

OBJECTIVES: I. Determine the safety of total body irradiation and fludarabine followed by allogeneic peripheral blood stem cell or bone marrow transplantation in combination with cyclosporine and mycophenolate mofetil for establishing mixed chimerism in patients with inherited disorders.

II. Determine whether this regimen can establish mixed chimerism in these patients.

III. Determine whether mixed chimerism is sufficient to reverse disease symptoms in these patients.

IV. Determine the safety of donor lymphocyte infusions to eliminate persistent disease in these patients with mixed chimerism.

Description:

PROTOCOL OUTLINE: Patients receive fludarabine IV over 2 hours on days -4 to -2 followed by total body irradiation and peripheral blood stem cell or bone marrow transplantation on day

0. Patients also receive oral or IV cyclosporine 2-3 times daily on days -3 to 50 (related donor) or 100 (unrelated donor) and oral mycophenolate mofetil twice daily on days 0 to 28 (related donor) or 40 (unrelated donor).

Patients may also receive donor lymphocyte infusion for continued treatment of symptoms in the event of mixed chimerism and in the absence of graft-versus-host disease.

Patients are followed weekly for 1 month, monthly for 2 years, and then annually thereafter.

Other known NCT identifiers

• NCT00144742

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. primary completion date: April 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A to 55 Years

Eligibility

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

• Inherited disorders treatable with allogeneic peripheral blood or bone marrow transplantation At high risk for regimen related toxicity with a conventional transplant

• No severe CNS involvement of disease, defined by IQ score less than 70

• HLA matched donor Sibling donors must be a confirmed match at HLA-A, B, and DRB1 Other related and non-related donors must be matched at HLA-A, B, C, DRB1, and DQB1 A donor homozygous for one allele only at HLA-A, B, C, DRB1, or DQB1 allowed (1 antigen mismatch for graft-versus-host disease, 0 antigen mismatch for graft-rejection)

--Prior/Concurrent Therapy--

• No concurrent growth factors with mycophenolate mofetil

--Patient Characteristics--

• Age: Under 55

• Performance status: Not specified

• Life expectancy: At least 100 days

• Hematopoietic: Not specified

• Hepatic: No evidence of synthetic dysfunction No severe cirrhosis

• Renal: Not specified

• Cardiovascular: LVEF at least 30% No poorly controlled hypertension on multiple antihypertensives

• Other: No organ dysfunction that would preclude survival Not pregnant or nursing Fertile patients must use effective contraception during and for 12 months following study

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

• Chronic Disease
• Granuloma
• Granulomatous Disease, Chronic
• Metabolism, Inborn Errors

Intervention

Drug:
• cyclosporine

• fludarabine

• mycophenolate mofetil

Locations

Country	Name	City	State
United States	Fred Hutchinson Cancer Research Center	Seattle	Washington

Sponsors (1)

Lead Sponsor	Collaborator
Fred Hutchinson Cancer Research Center

Country where clinical trial is conducted

United States,