A Study of the Effectiveness of an HIV Vaccine (ALVAC vCP205) to Boost Immune Functions in HIV-Negative Volunteers Who Have Already Received an HIV Vaccine
Launched by NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES (NIAID) · Aug 30, 2001
Trial Information
Current as of May 09, 2025
Completed
Keywords
ClinConnect Summary
Vaccines may provide a route of therapy against HIV-1 infections by boosting the immune system responses. An artificially constructed HIV-1 vaccine (NYCBH), using vaccinia virus as its vector, has the advantage of conferring both cellular and humoral immune responses that are long-lived. Studies have shown that a second artificially constructed vector vaccine, HIV-1 canarypox (vCP205), also increases CD8+ cytotoxic T lymphocyte (CTL) activity, a cell-mediated immune response. Yet, immune responses are not boosted in volunteers previously vaccinated with vaccinia-based HIV-1 vaccines when a ...
Gender
ALL
Eligibility criteria
- • Inclusion Criteria
- You may be eligible for this study if you:
- • Are 18-60 years old.
- • Are willing to use adequate birth control for 1 month before study entry and during the study.
- • Have a CD4 count of at least 400 cells/mm3.
- • Have a normal medical history and physical examination.
- • Are available for 3 months of follow-up.
- • Have participated in AVEG Protocol 014C or 022A and received all the scheduled vaccinations 24 or more months before this study, or have never participated in HIV-vaccine studies.
- • Are HIV-negative within 8 weeks of study entry.
- • Are negative for hepatitis B surface antigen.
- • Exclusion Criteria
- You will not be eligible for this study if you:
- • Are pregnant or breast-feeding.
- • Have a history of an immune system problem, any long-term illness, or any autoimmune disease.
- • Have a history of using medications which affect your immune system.
- • Have a history of cancer, except if it has been removed with surgery and cure is most likely.
- • Have a medical or mental condition which interferes with the study.
- • Have a job or work which interferes with the study.
- • Have ever attempted suicide, thought of attempting suicide, or have a severe mental condition.
- • Have received vaccines within 60 days of study entry.
- • Have used experimental drugs within 30 days prior to study entry.
- • Have received any blood products, such as immunoglobulin, in the last 6 months.
- • Have active syphilis.
- • Have active tuberculosis.
- • Have any history of severe allergic reactions, including reactions to vaccines.
- • Have an allergy to egg products or neomycin.
About National Institute Of Allergy And Infectious Diseases (Niaid)
The National Institute of Allergy and Infectious Diseases (NIAID) is a key component of the National Institutes of Health (NIH) dedicated to advancing the understanding, prevention, and treatment of infectious and immune-mediated diseases. Through rigorous clinical trials, NIAID aims to foster innovative research that enhances public health and addresses global health challenges, including emerging infectious diseases and allergies. The institute collaborates with various partners, including academic institutions, industry, and international organizations, to translate scientific discoveries into effective therapies and vaccines. NIAID's commitment to high-quality clinical research is integral to improving health outcomes and informing policy decisions in the realm of infectious diseases and immunology.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Nashville, Tennessee, United States
Rochester, New York, United States
Birmingham, Alabama, United States
Baltimore, Maryland, United States
Saint Louis, Missouri, United States
Seattle, Washington, United States
Patients applied
Trial Officials
Thomas Evans
Study Chair
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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