A Phase I Clinical Trial to Evaluate the Safety and Immunogenicity of 200 Mcg of gp120 (CHO) BIOCINE in MF59 Emulsion Versus the Emulsion Control: Three Injections at 0, 1, and 6 Months

Completed · Phase 1

Conditions studied: HIV Infections

In brief

To evaluate in healthy volunteers the safety and immune response to 200 mcg gp120 candidate vaccine in MF59 emulsion without MTP-PE at 0, 1 and 6 months. Preliminary evaluations of two dose levels of gp120 administered to volunteers in protocol VEU 007A indicate that a gp120 dose of potentially greater immunogenicity may be of interest.

Key facts

Study ID

NCT00000749

Run by

National Institute of Allergy and Infectious Diseases (NIAID)

People needed

14

Last updated by the study team

2012-10-30

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects must have:
• Normal history and physical exam.
• Negative ELISA for HIV.
• Normal cell-mediated immune responses using Merieux skin test.
• Normal urinalysis.

You may not qualify if…

• Co-existing Condition:
• Subjects with the following conditions are excluded:
• Evidence of psychological or psychiatric problems that may lead to noncompliance with study requirements.
• Positive syphilis serology. If serology is documented as a false positive or is due to a remote (> 6 months) treated infection, subject is eligible.
• Circulating hepatitis B surface antigen.
• Subjects with the following prior conditions are excluded:
• History of immunodeficiency, chronic illness, autoimmune disease, or use of immunosuppressive medications.
• History of anaphylaxis or other adverse reactions to vaccines.
• Prior Medication:
• Excluded:
• Prior HIV vaccines.
• Immunoglobulins or vaccines within the past 3 months.
• Experimental agents within the past 30 days.
• Prior Treatment:
• Excluded:
• Blood transfusions or cryoprecipitates within the past 3 months.
• Identifiable high-risk behavior for HIV infection, including:
• Any history of intravenous (IV) drug use within the past year.
• Syphilis, gonorrhea, or any other sexually transmitted diseases (including chlamydia or pelvic inflammatory disease) in the past 6 months.
• More than two sexual partners, or sexual contact with a high-risk partner, in the past 6 months.

Where it is running

• Vanderbilt Univ Hosp — Nashville, Tennessee, United States
• Univ of Washington / Pacific Med Ctr — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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