- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00051454
Evaluation of the Safety of and Immune Response to an HIV Vaccine in Healthy Adults
A Randomised, Placebo-Controlled, Double-Blind, Phase I/IIa Clinical Trial to Evaluate the Safety and Immunogenicity of a Candidate Prophylactic DNA Prime-rFPV Boost HIV Vaccination Strategy
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
The purpose of this study is to examine the safety and immunogenicity of a candidate vaccine strategy for HIV prophylaxis using a DNA-prime plus recombinant fowlpox boost. The DNA plasmid and fowlpox vector contain HIV genes. However, these vaccines contain only some HIV genes and cannot themselves cause HIV or AIDS.
Eligible volunteers at low risk of HIV infection will be randomized to receive either active vaccine or placebo injections at Day 0, Week 4, and Week 8. Intensive immunologic and safety monitoring will be done during the first 16 weeks of the study. Follow-up will continue to Week 52.
Studietype
Registrering
Fase
- Fase 2
- Fase 1
Kontakter og plasseringer
Studiesteder
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New South Wales
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Sydney, New South Wales, Australia, 2010
- National Centre in HIV Epidemiology and Clinical Research
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria
- HIV negative.
- Acceptable methods of contraception.
Exclusion Criteria
- Identifiable risk behavior for HIV infection, including: sexual partners of HIV positive people, sexual intercourse with a partner of unknown HIV status if that partner is reported to be at higher risk for HIV infection, gay men reporting any unprotected anal intercourse with partners of unknown status in the 12 months preceding study entry, individuals diagnosed with a sexually transmissible infection (STI) in the 12 months preceding entry that may have been acquired through anal or vaginal intercourse, individuals reporting sharing of injecting equipment in the last 12 months.
- HIV candidate vaccines in a previous HIV vaccine trial.
- Live attenuated vaccines within 60 days prior to entering the study. Whole killed, toxoid, or sub-unit vaccines (e.g., influenza, pneumococcal, tetanus, and hepatitis B) are not exclusionary within 4 weeks prior to the scheduled experimental HIV vaccines.
- Hypersensitivity to egg products or a known history of anaphylaxis or any other serious adverse reactions to vaccination.
- History of serious allergic reaction requiring hospitalization or emergency medical care (e.g., Stevens-Johnson syndrome, bronchospasm, or hypotension) to any substance.
- Significant illness requiring immunomodulatory or cytotoxic therapy.
- History of cancer unless there is evidence of surgical excision followed by a sufficient observation period to give a reasonable assurance of cure.
- Blood products or immunoglobulins within 6 months prior to entering the study.
- Experimental or investigational agents within 30 days prior to entering the study.
- Recreational and/or therapeutic drug use that might compromise the study participant's safety.
- Medical or psychiatric condition or occupational responsibilities that preclude compliance with the protocol.
- Pregnant or lactating women.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Hva måler studien?
Primære resultatmål
Resultatmål |
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Safety and adverse events among the two vaccination groups
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lymphoproliferative (LP) responses to HIV antigens, as assessed by LP assays at Week 9
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CD8+ T cell responses to HIV antigens, as assessed by ELIspot assay of interferon gamma (IFN-g) secreting cells at Week 9
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Sekundære resultatmål
Resultatmål |
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Proportion of patients with positive LP assay and ELISPOT assay responses
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intracellular cytokine staining (ICS) of IFN-g/CD69 and flow cytometry
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51-Cr release cytotoxic T cell lymphocyte assay
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HLA class I tetramer analyses
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anti-HIV gag, pol and env antibodies, as assessed by ELISA and Western blot
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behavioral changes in study participants
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Samarbeidspartnere og etterforskere
Etterforskere
- Studieleder: David A Cooper, MD, DSc, National Centre in HIV Epidemiology and Clinical Research, University of New South Wales
Publikasjoner og nyttige lenker
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Studierekorddatoer
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Studiestart
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Oppdateringer av studieposter
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Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- N01-AI05395
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