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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00152100
Other study ID # ALSCID
Secondary ID
Status Completed
Phase Phase 1
First received September 7, 2005
Last updated May 19, 2009
Start date February 2004
Est. completion date August 2007

Study information

Verified date May 2009
Source St. Jude Children's Research Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Treatment for severe combined immunodeficiency (SCID) is a medical emergency. A stem cell transplant (immature blood cells that can make other blood cells) from a (MSD) matched sibling donor (brother or sister who is a "match" for your child's immune (HLA) type), usually results in complete correction of immune function. However, most patients lack a matched sibling donor, requiring the use of an alternate donor source.

Transplantation of cells from haploidentical family donors (typically parents) has resulted in immune system correction in the majority of SCID individuals. However, only 65-80% of patients survive greater than one year after this procedure. Failure results from life-threatening infections, graft versus host disease (GvHD) or post-transplant treatment-related effects. Also, for patients that survive beyond one year, B-cell (type of blood cell that fights infection) and natural killer cell function (cell that attacks infections and cancer cells) frequently fail to work, resulting in the need for long-term treatment with intravenous gamma-globulin (IVIg).

In this study, in an effort to restore the overall cell function in patients with SCID, researchers will use a highly purified CD133+ hematopoietic cell graft (stem cell transplant without many mature donor white cells, called T-cells) obtained via use of the Miltenyi CliniMACS device, a device not FDA approved.


Recruitment information / eligibility

Status Completed
Enrollment 4
Est. completion date August 2007
Est. primary completion date August 2007
Accepts healthy volunteers No
Gender Both
Age group N/A to 2 Years
Eligibility Inclusion Criteria:

- Patient with confirmed severe combined immunodeficiency

- Two years of age or younger

- A suitable matched sibling donor is not available

Exclusion Criteria:

- An available matched sibling donor or a confirmed matched unrelated donor

- Patients with DiGeorge syndrome, Zap70, MHC Class II deficiency, or cartilage-hair hypoplasia

- Patients with a Lansky performance score of less than 10, evidence of HIV or a congenital rubella infection or a documented neoplasm

- Patients in whom it is not possible to perform a peripheral blood cell harvest on a haploidentical family member

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Procedure:
Stem cell transplant

Drug:
Filgrastim, Alemtuzumab

Device:
Miltenyi CliniMACS


Locations

Country Name City State
United States St. Jude Children's Research Hospital Memphis Tennessee

Sponsors (1)

Lead Sponsor Collaborator
St. Jude Children's Research Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To investigate safety issues related to use of haploidentical highly purified CD133+ hematopoietic cells in patients with SCID
Primary To study the effects (good and bad) of this procedure
Primary To learn if this procedure will result in normal immune function in children with SCID
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