Effectiveness of Adding Remune to Your Current Anti-HIV Drug Combination

HIV Infections Clinical Trial

Official title:

A Multicenter, Double-Blind, Phase I, Adjuvant Controlled Study to Evaluate the Effect of Remune (HIV-1 Immunogen) Compared to IFA, in Combination With Fully Suppressive Antiviral Drug Therapy on HIV-1-Specific Immunogenicity in Subjects With Acute or Primary HIV-1 Infection

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00006153
• Other study ID #: AIEDRP AI-05-006
• Secondary ID: 905
• Status: Terminated
• Phase: Phase 1
• First received: August 7, 2000
• Last updated: July 29, 2008

Study information

• Verified date: June 2003
• Source: National Institute of Allergy and Infectious Diseases (NIAID)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to see if giving a vaccine (Remune) is effective in HIV-positive patients who are also taking anti-HIV therapy.

Regular treatment of HIV-positive patients with anti-HIV drugs slows the multiplication of the HIV virus in the body. A vaccine called Remune works to stop the virus infection by "boosting" the body's immune cell defense against the HIV virus before the virus enters cells. It also blocks the virus from entering the cells. This study will see whether Remune will improve the immune cell natural defense in patients who are also taking anti-HIV drugs.

Description:

During primary HIV infection, after an initial burst in viral load, the body mounts an immunologic response to viral antigens. It is thought that this initial immune response plays an important role in determining early and long-term suppression of HIV. However, limited information is available regarding the effect of early antiretroviral therapy on immune responses. Therapeutic approaches such as Remune, which augment cell-mediated immunologic responses, may prove to be beneficial in controlling the progression of HIV infection, especially when used in combination with antiretroviral therapy in early infection. Current antiviral drugs work by inhibiting the infection of new cells yet seem to suppress early cell-mediated immune responses. The question is raised as to whether immune-based therapies such as Remune may counteract the suppressive effects of antiretrovirals and slow the progression of infection.

Patients receiving fully suppressive antiretroviral therapy are randomized to add either Remune or an Incomplete Freund's Adjuvant (IFA) control. Vaccinations are administered on Day 1, Week 12, and Week 24. Blood samples are collected at Day 1 and Weeks 4, 12, 16, 24, and 28. Clinical assessment includes lymphocyte proliferative response, cytotoxic T lymphocyte (CTL) memory cell activity, chemokine and cytokine measurements, CD4 count, and viral load. Delayed-type hypersensitivity (DTH) skin tests are performed at Day 1 and Week

28. HIV-1 specific immunogenicity is coordinated with the response to antiretroviral therapy in patients.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 45
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 16 Years and older

Eligibility

Inclusion Criteria

Patients may be eligible for this study if they:

• Are HIV-positive and started anti-HIV drugs soon after tests showed the presence of HIV.

• Have been on an anti-HIV drug combination that includes a protease inhibitor for at least 3 months but no longer than 12 months.

• Have 2 consecutive viral loads of less than 50 copies/ml, at least 30 days apart, within 90 days of study entry.

• Are at least 16 years old (consent of parent or guardian required if under 18 years).

• Agree to practice abstinence or use effective methods of birth control during the study.

Exclusion Criteria

Patients will not be eligible for this study if they:

• Are pregnant or breast-feeding.

• Currently abuse alcohol or drugs.

• Are currently being treated for some types of cancer.

• Have any illness or condition that might interfere with the study or put them at risk.

• Have received a vaccination 6 weeks before study entry.

• Have previously received Remune.

• Are taking medications that affect the immune system within 30 days of study entry.

Study Design

Endpoint Classification: Safety Study, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• HIV Infections

Intervention

Biological:
• HIV-1 Immunogen

Locations

Country	Name	City	State
United States	Joanne Santangelo	San Diego	California

Sponsors (2)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)	The Immune Response Corporation

Country where clinical trial is conducted

United States, 

External Links

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