Safety and Immunogenicity of Rgp 120/HIV-1IIIB Vaccine in HIV-1 Positive Adults
rgp120/HIV-1IIIB
Blood-Borne Infections+13
+ Urogenital Diseases
+ Genital Diseases
Prevention Study
Summary
This study focuses on the safety and effectiveness of a vaccine called rgp 120/HIV-1IIIB in adults who are HIV-1 seropositive, meaning they have tested positive for HIV-1. The main goal is to prevent HIV-1 from causing further harm. This research is important as it could potentially improve the care and treatment options for individuals living with HIV-1, addressing the current challenges in managing this condition.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria Patients must have the following: Stage 1 or 2 Walter Reed clinical staging of HIV infected individuals. The ability to understand and sign a written informed consent form, which must be obtained prior to study entry. Be available for 24 weeks so that follow up may be completed. Qualify for care as Department of Defense health care beneficiary. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Prior history of clinically significant cardiac, pulmonary, hepatic, renal, neurologic or autoimmune disease, other than HIV-1 infection, and in less than average general health as determined by a medical history, physical examination, and the required laboratory test results. Concurrent Medication: Excluded: Corticosteroids or other known immunosuppressive drugs. Any experimental agents. Patients with the following are excluded: Prior history of clinically significant cardiac, pulmonary, hepatic, renal, neurologic or autoimmune disease, other than HIV-1 infection, and in less than average general health as determined by a medical history, physical examination, and the required laboratory test results. Prior Medication: Excluded within 30 days of study entry: Zidovudine or other anti-retroviral agents.
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Walter Reed Army Institute of Research
Rockville, United StatesOpen Walter Reed Army Institute of Research in Google Maps