Gene Transfer for HIV Using Autologous T Cells
NCT01153646 · Status: TERMINATED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 5
Last updated 2011-01-19
Summary
This is a pilot study to determine the safety and feasibility of lentivirus-transduced T-cell immunotherapy in patients who have failed highly active anti-retrovirus therapy (HAART).
Conditions
- HIV-1 Infection
Interventions
- GENETIC
-
pHIV7-shI-TAR-CCR5RZ treated CD4 cells
Single dose administration x 3 of genetically modified T-cells given at 3 infusions at 6 week intervals.
Sponsors & Collaborators
-
City of Hope Medical Center
lead OTHER
Principal Investigators
-
John A. Zaia, MD · Beckman Research Institute of City of Hope
Study Design
- Allocation
- NA
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-04-30
- Primary Completion
- 2011-01-31
- Completion
- 2011-01-31
Countries
- United States
Study Locations
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