NCT Number: NCT00000779
A Phase I Comparative Blinded Trial of Several HIV-1 Derived Immunogens in Infected Individuals With >= 500 CD4 Cells/mm3
PRIMARY: To compare the immunogenicity and safety of each of several HIV-1 derived immunogens versus control in HIV-infected individuals with CD4 counts greater than or equal to 500 cells/mm3.
SECONDARY: To determine whether significant advantages to any one vaccine exist.
Before large clinical trials of anti-HIV vaccines are undertaken, it is important to determine whether there are significant advantages to any one of the vaccines currently offered for such studies.
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Notify MeKey information
Conditions
Age range
13 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
UCLA CARE Center CRS, Los Angeles, California, United States
About this study
Before large clinical trials of anti-HIV vaccines are undertaken, it is important to determine whether there are significant advantages to any one of the vaccines currently offered for such studies.
Patients are randomized to receive one of four vaccines or one of two placebo controls. The vaccines are: rgp 120/HIV-1IIIB, rgp 120/HIV-1MN, rgp 120/HIV-1SF, and env 2-3. The two control immunogens are aluminum hydroxide (alum) and BIOCINE Placebo Vaccine 2 (MF-59 adjuvant emulsion in citrate buffer). Patients are vaccinated at weeks 0, 4, 8, 12, 16, 20, 28, and 36. If significant benefit is seen among vaccine patients, then placebo patients may receive vaccination with one of the immunogens producing an immune response.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Concurrent Medication:
Allowed:
- Short-term nonsteroidal anti-inflammatory therapy.
Patients must have:
- HIV seropositivity.
- CD4 count >= 500 cells/mm3.
- Successful establishment of EBV-transformed B-cell lines at study entry.
- Consent of parent or guardian if < 18 years of age.
Exclusion criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Suspected or known allergies to any vaccine components.
- Medical contraindication.
- Problem with compliance.
Concurrent Medication:
Excluded:
- Antiretroviral therapy (e.g., AZT, ddI, or ddC).
- Agents with putative immunomodulating activity (e.g., interferon, steroids, hematopoietin).
- Parenteral therapies (including SC allergy sensitization).
- Other investigational HIV drugs or therapies.
Prior Medication:
Excluded:
- Any prior vaccinations against HIV.
- Antiretroviral therapy (e.g., AZT, ddI, or ddC) within the past 6 months.
- Agents with putative immunomodulating activity (e.g., interferon, steroids, hematopoietin) within the past 3 months.
- Parenteral therapies (including SC allergy sensitization) within the past 3 months.
- Other investigational HIV drugs or therapies within the past 3 months.
Treatment and study plan
MF59
Biologicalrgp120/HIV-1IIIB
Biologicalrgp120/HIV-1MN
Biologicalrgp120/HIV-1 SF-2
BiologicalEnv 2-3
BiologicalSponsors and collaborators
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Nih
Registry information
Important dates
- Study completion
- 1996
- First posted
- Aug 31, 2001
- Registry last updated
- Nov 4, 2021
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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