A Pilot Study to Investigate the Safety and Immunologic Activity AGS-004 an Autologous HIV Immunotherapeutic Agent.

McGill University

Status and phase: Completed; Phase 2; Phase 1

Conditions: Acquired Immunodeficiency Syndrome; HIV Seropositivity

Treatments: Biological: AGS-004

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00381212

CAN-HIV-001

CTN229

BMB#06-003

Details and patient eligibility

About

To Investigate the safety and immunologic activity of AGS-004, an autologous HIV Immunotherapeutic, in HIV-infected adults currently on stable antiretroviral therapy (ART) with durable viral suppression.

Full description

Although an HIV infection can induce weak immune responses, current HIV immunotherapy using consensus antigens has not shown consistent clinical activity. The absence of clinical activity is associated with an inability to raise cytotoxic T lymphocytes (CTL) against HIV antigens and a failure to induce T cell memory. While strong immune responses may be generated to a consensus antigen, those responses do not offer antiviral protection against a patient's individual viral burden. The infecting virus' antigen variability likely prevents the establishment of effective CD4+ T cell memory and a strong CD8+ T cell effector arm.

We are investigating the induction of CTL responses in HIV-infected subjects by a novel HIV immunotherapeutic agent (AGS-004) in an effort to overcome the lack of polyvalent specificity of the immune response for autologous HIV antigens which has been one of the primary reasons for the failure of HIV immunotherapy to date.

This pilot study will investigate the safety and immunologic activity of AGS-004 an autologous HIV immunotherapeutic agent.

Enrollment: 10 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Men or women age 18 years and over,
• Documented HIV-1 infection,
• Durable viral suppression (≤ 200 copies HIV-1 RNA / mL) on first ART regimen for at least 12 weeks prior to entry,
• Availability of ≥ 2.5mL of continually-frozen plasma before starting ART (≥30,000 copies/mL),
• CD4+ T cell count ≥200 cells/mm3 at time of pre-ART sample,
• CD4+ T cell count of ≥350 cells/mm3 obtained within 4 weeks of study entry,

Exclusion criteria

• No co-infection with HBV or HCV,
• No history of lymph node irradiation or dissection,
• No prior use of any HIV vaccine,
• No use of hydroxyurea,
• No use of systemic corticosteroids or other non-permitted medications,

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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10 participants in 1 patient group

1

Experimental group

Description:

AGS-004 immunotherapeutic injections.

Treatment:

Biological: AGS-004