Chiron Vaccine HIV p24/MF59 Safety and Immunogenicity in Healthy Adults
This phase 1 study aims to evaluate the safety and ability to trigger an immune response of the Chiron Vaccine HIV p24/MF59 in healthy adults.
HIV p24/MF59 Vaccine
Blood-Borne Infections+11
+ Urogenital Diseases
+ Genital Diseases
Prevention Study
Summary
This study evaluates the safety and immunogenicity of the Chiron vaccine HIV p24/MF59. In Part A, 15 volunteers are randomly assigned to receive either HIV p24/MF59 or a placebo at 0, 1, and 6 months. 10 volunteers receive the vaccine and 5 volunteers receive the placebo. If no serious adverse events are observed within 1 week after the first injection in these first 15 patients, Part B is initiated. In Part B, 25 volunteers are randomly assigned to receive HIV p24/MF59 or a placebo at 0, 1, and 6 months. 20 volunteers receive the vaccine and 5 volunteers receive the placebo.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.40 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.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.From 18 to 50 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria Volunteers must have: Good health as determined by medical history, physical examination, and clinical judgment. Negative serology for HIV infection as determined by licensed HIV ELISA test performed within 6 weeks prior to first immunization. In vitro Epstein-Barr virus-immortalized cell line from peripheral blood can be established (required for selected Part B volunteers only). Exclusion Criteria Co-existing Condition: Volunteers with the following symptoms or conditions are excluded: Significant acute systemic infection. Occupational or other responsibilities that would prevent completion of participation in the study. Any condition that might interfere with the evaluation of the study objectives. Volunteers with the following prior conditions are excluded: History of immunodeficiency, autoimmune disease, or any serious chronic illness. Evidence of psychiatric or medical history or substance abuse that would adversely affect the volunteer's ability to participate in the trial. History of anaphylaxis or other serious adverse reactions to vaccines or vaccine components. 1. Immunosuppressive medications. Live, attenuated vaccine within 60 days of study entry. NOTE: Medically indicated subunit or killed vaccines (e.g., influenza or pneumococcal) are not exclusionary but should be given at least 4 weeks before or after HIV immunizations to avoid potential confusion of adverse reactions. Experimental agents within 30 days of study entry. HIV vaccine or MF59 adjuvant. Blood products or immunoglobulins in the past 3 months. Engaging in high-risk behavior within 6 months of study entry, i.e.: injection drug use, sexual intercourse without a condom with 4 or more partners or with known iv drug user or HIV+ partner, or newly acquired sexually-transmitted disease.
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
Creighton Univ Med Ctr / Ped Infect Disease Div
Omaha, United StatesOpen Creighton Univ Med Ctr / Ped Infect Disease Div in Google Maps