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Safety and Anti-HIV Activity of Autologous CD4+ and CD8+ T Cells Transduced With a Lentiviral Vector Encoding Bi-specific Anti-gp120 CAR Molecules (LVgp120duoCAR-T) in Anti-retroviral Drug-treated HIV-1 Infection

Who is this study for? Patients with HIV-1 Infection
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Biological, Other, Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

This is a limited-center, open-label dose escalating phase I/IIa study of autologous T cells expressing LVgp120duoCAR molecules in people with HIV infection. It will follow a 3+3 design. Dose escalation decisions will be made when a minimum of three participants have completed the safety-evaluation period (45 days) at a given dose level. Cohort 1 will undergo infusion of a single low-dose regimen of LVgp120duoCAR-T cells. Cohort 2 will undergo non-ablative conditioning with cyclophosphamide, followed by infusion of a single low-dose regimen of LVgp120duoCAR-T cells. Cohort 3 will undergo non-ablative conditioning with cyclophosphamide, followed infusion of a single high-dose regimen of LVgp120duoCAR-T cells. Following administration of the experimental therapy, HIV medications will be paused for participants in each group during an analytic treatment interruption.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Male or female, age ≥ 18 and ≤ 65 years

• HIV-1 infection

• On continuous antiretroviral therapy for at least 12 months without any interruptions of greater than 14 consecutive days, and on a stable regimen that does not include a non-nucleoside reverse transcriptase inhibitor (NNRTI) for at least 4 weeks or any long-acting ART drug that may be active in the participant after ART interruption for up to one year, without plans to modify ART during the study period

• Screening plasma HIV RNA levels below the limit of quantification on all available determinations in past 12 months (isolated single values ≥ 40 but \< 200 copies/mL will be allowed if they were preceded and followed by undetectable viral load determinations)

• CD4+ T cell count nadir \> 300 cells/mm3

• Screening CD4+ T-cell count ≥ 500 cells/mm3

• Available ART treatment history and the capacity to construct an effective antiretroviral treatment regimen

• Willing to pause ART as part of the study

Locations
United States
California
University of California, Davis
RECRUITING
Sacramento
Zuckerberg San Francisco General
RECRUITING
San Francisco
Contact Information
Primary
Rebecca Hoh
rebecca.hoh@ucsf.edu
415-476-4082
Time Frame
Start Date: 2021-03-01
Estimated Completion Date: 2029-12-31
Participants
Target number of participants: 18
Treatments
Experimental: Low Dose CAR-T Cells Only
Participants will NOT undergo non-ablative conditioning with cyclophosphamide. A single dose of 3 x 10\^5 cells/kg LVgp120duoCAR-T cells will be infused. ART will be interrupted immediately after infusion.
Experimental: Conditioning + Low Dose CAR-T Cells
Participants will undergo non-ablative conditioning with cyclophosphamide. A single dose of 3 x 10\^5 cells/kg LVgp120duoCAR-T cells will be infused. ART will be interrupted immediately after infusion.
Experimental: Conditioning + High Dose CAR-T Cells
Participants will undergo non-ablative conditioning with cyclophosphamide. A single dose of 1 x 10\^6 cells/kg LVgp120duoCAR-T cells will be infused into the participant. ART will be interrupted immediately after infusion.
Related Therapeutic Areas
Sponsors
Leads: Steven Deeks
Collaborators: Caring Cross

This content was sourced from clinicaltrials.gov