Setting up a Blood Bank for Gene Therapy in HIV-Infected Infants
Primary Purpose
HIV Infections, Pregnancy
Status
Terminated
Phase
Locations
United States
Study Type
Observational
Intervention
Sponsored by

About this trial
This is an observational trial for HIV Infections focused on measuring Gene Therapy, Specimen Handling, Blood Banks, Fetal Blood
Eligibility Criteria
Inclusion Criteria You may be eligible for this study if you: Are HIV-positive. Exclusion Criteria Your child will not be eligible for this study if he/she: Is not expected to live more than 6 months. Weighs less than 3.3 pounds.
Sites / Locations
- UCSD Med Ctr / Pediatrics / Clinical Sciences
- Long Beach Memorial (Pediatric)
- Los Angeles County - USC Med Ctr
- Cedars Sinai / UCLA Med Ctr
- UCLA Med Ctr / Pediatric
- Harbor - UCLA Med Ctr / UCLA School of Medicine
- San Francisco Gen Hosp
- UCSF / Moffitt Hosp - Pediatric
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00000917
First Posted
November 2, 1999
Last Updated
July 30, 2008
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
1. Study Identification
Unique Protocol Identification Number
NCT00000917
Brief Title
Setting up a Blood Bank for Gene Therapy in HIV-Infected Infants
Official Title
Establishment of a Cord Blood Bank for Gene Therapy in HIV-Infected Infants
Study Type
Observational
2. Study Status
Record Verification Date
June 2003
Overall Recruitment Status
Terminated
Study Start Date
September 1997 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
4. Oversight
5. Study Description
Brief Summary
The purpose of this study is to set up a blood bank for infants who have HIV-positive mothers. This blood may be used in the future to treat the child if he/she turns out to be HIV-positive.
Blood from the umbilical cord contains a certain kind of cell called a stem cell. Stem cells eventually turn into one of the many types of blood cells. If HIV infection can be prevented in these stem cells, then, when these stem cells are injected back into the infant, the new cells that develop will also be protected from HIV. This study will provide the blood needed to test whether this type of gene therapy is safe and effective.
Detailed Description
Gene therapy may provide a new therapeutic approach to pediatric AIDS. Putting an HIV-resistant gene into umbilical cord blood stem cells and transplanting the cells back into the patient could lead to the production of cells that resist HIV infection. If a patient's cells could be engineered to be resistant to supporting the growth of HIV-1, the cells may have improved survival in the presence of HIV-1. To date, an umbilical cord blood bank for HIV-positive deliveries has not been established in the United States. This protocol establishes a repository of banked umbilical cord blood as a first step toward the potential application of gene therapy for the treatment of HIV-infected infants.
HIV-infected mothers have about 20 ml of blood drawn to test for infectious diseases (e.g., hepatitis). At time of delivery maternal HIV viral load is measured. After delivery, about 60 ml of blood is collected from the umbilical cord; this blood is labeled and transferred to the umbilical cord blood bank for possible use in future gene therapy studies on the infant. At birth, infant HIV status and general health are assessed. If the infant is found to be HIV-infected, the mother may be approached about the infant's participation in a future gene therapy study. If the infant is not HIV-infected, the cord blood is stored for up to four years and is then released to the mother, or, with her consent, to the research community.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Pregnancy
Keywords
Gene Therapy, Specimen Handling, Blood Banks, Fetal Blood
7. Study Design
Enrollment
200 (false)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
6 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
You may be eligible for this study if you:
Are HIV-positive.
Exclusion Criteria
Your child will not be eligible for this study if he/she:
Is not expected to live more than 6 months.
Weighs less than 3.3 pounds.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Savita Pahwa
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Howard Rosenblatt
Official's Role
Study Chair
Facility Information:
Facility Name
UCSD Med Ctr / Pediatrics / Clinical Sciences
City
La Jolla
State/Province
California
ZIP/Postal Code
920930672
Country
United States
Facility Name
Long Beach Memorial (Pediatric)
City
Long Beach
State/Province
California
ZIP/Postal Code
90801
Country
United States
Facility Name
Los Angeles County - USC Med Ctr
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Facility Name
Cedars Sinai / UCLA Med Ctr
City
Los Angeles
State/Province
California
ZIP/Postal Code
900481804
Country
United States
Facility Name
UCLA Med Ctr / Pediatric
City
Los Angeles
State/Province
California
ZIP/Postal Code
900951752
Country
United States
Facility Name
Harbor - UCLA Med Ctr / UCLA School of Medicine
City
Los Angeles
State/Province
California
ZIP/Postal Code
905022004
Country
United States
Facility Name
San Francisco Gen Hosp
City
San Francisco
State/Province
California
ZIP/Postal Code
94110
Country
United States
Facility Name
UCSF / Moffitt Hosp - Pediatric
City
San Francisco
State/Province
California
ZIP/Postal Code
941430105
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Setting up a Blood Bank for Gene Therapy in HIV-Infected Infants
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