Expired Study
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Rockville, Maryland 20850


Purpose:

To test the safety and immunogenicity of rgp 120/HIV-1IIIB vaccine in HIV-1 seropositive adult patients.


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.


NCT ID:

NCT00001992


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Rockville, Maryland 20850
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 21, 2017

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