Ignite Creation Date:
2025-12-24 @ 12:19 PM
Ignite Modification Date:
2026-01-02 @ 6:33 AM
Study NCT ID:
NCT00002261
Status:
COMPLETED
Last Update Posted:
2007-09-26
First Post:
1999-11-02
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
A Comparative Phase I Clinical Study of HIVAC-1e and Smallpox (Vaccinia) Vaccines in Previously (Vaccinia) Vaccinated and Unvaccinated Volunteers
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D015658', 'term': 'HIV Infections'}, {'id': 'D014615', 'term': 'Vaccinia'}], 'ancestors': [{'id': 'D000086982', 'term': 'Blood-Borne Infections'}, {'id': 'D003141', 'term': 'Communicable Diseases'}, {'id': 'D007239', 'term': 'Infections'}, {'id': 'D015229', 'term': 'Sexually Transmitted Diseases, Viral'}, {'id': 'D012749', 'term': 'Sexually Transmitted Diseases'}, {'id': 'D016180', 'term': 'Lentivirus Infections'}, {'id': 'D012192', 'term': 'Retroviridae Infections'}, {'id': 'D012327', 'term': 'RNA Virus Infections'}, {'id': 'D014777', 'term': 'Virus Diseases'}, {'id': 'D000091662', 'term': 'Genital Diseases'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D007153', 'term': 'Immunologic Deficiency Syndromes'}, {'id': 'D007154', 'term': 'Immune System Diseases'}, {'id': 'D011213', 'term': 'Poxviridae Infections'}, {'id': 'D004266', 'term': 'DNA Virus Infections'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D012900', 'term': 'Smallpox Vaccine'}, {'id': 'C067702', 'term': 'HIVAC-1e'}, {'id': 'C053473', 'term': 'VaxSyn HIV-1 (gp160) vaccine'}], 'ancestors': [{'id': 'D014765', 'term': 'Viral Vaccines'}, {'id': 'D014612', 'term': 'Vaccines'}, {'id': 'D001688', 'term': 'Biological Products'}, {'id': 'D045424', 'term': 'Complex Mixtures'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'primaryPurpose': 'PREVENTION'}}, 'statusModule': {'overallStatus': 'COMPLETED', 'statusVerifiedDate': '2007-09', 'lastUpdateSubmitDate': '2007-09-24', 'studyFirstSubmitDate': '1999-11-02', 'studyFirstSubmitQcDate': '2001-08-30', 'lastUpdatePostDateStruct': {'date': '2007-09-26', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2001-08-31', 'type': 'ESTIMATED'}}, 'conditionsModule': {'keywords': ['Vaccines, Synthetic', 'Vaccinia Virus', 'Viral Vaccines', 'Smallpox Vaccine', 'HIV-1', 'AIDS Vaccines', 'HIV Seronegativity'], 'conditions': ['HIV Infections']}, 'descriptionModule': {'briefSummary': 'To determine the physiological and immunological responses in healthy HIV seronegative adult volunteers vaccinated with a) the HIVAC-1e (vaccinia-HIV) vaccine expressing the envelope glycoproteins of HIV and b) the Wyeth smallpox vaccine. The parameters to be studied will include:\n\n1. The course of physiological responses to vaccination, including (a) lesion development, progression, and resolution; (b) physiological changes such as temperature, malaise, itching at the site, etc. and (c) any observable AE.\n2. The appearance, identity, quantity, and duration of humoral antibodies against HIV and vaccinia virus.\n3. The appearance, identity, quantity, and duration of cell-mediated immunity against HIV and vaccinia virus.\n4. The adequacy of a procedure using a special dressing to contain viral shedding from the vaccination site.\n5. The safety, humoral and cellular immune responses of a booster injection of the recombinant subunit gp160 vaccine (MicroGeneSys) in HIVAC-1e recipients.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT'], 'maximumAge': '60 Years', 'minimumAge': '18 Years', 'healthyVolunteers': True, 'eligibilityCriteria': "Inclusion Criteria\n\nConcurrent Medication:\n\nAllowed:\n\n* All drugs, medications, and therapy which, by virtue of direct pharmacologic action or possible drug interaction, could influence the intended effects of the study vaccine or mask its side effects may be concomitantly administered only by prescription by the Principal Investigator and must be documented on the case report form (CRF).\n* Any drug, even aspirin, which is administered after vaccination and during the follow up periods must be documented on the patient's CRF.\n\nExclusion Criteria\n\nCo-existing Condition:\n\nPatients with the following conditions or symptoms are excluded:\n\n* Failure to meet any criteria listed under Inclusion Criteria.\n* Development of active eczema or other skin condition which would increase the risk of secondary vaccinia lesions.\n* Appearance of serologic or clinical evidence of HIV infection prior to vaccination.\n* Current evidence of clinically active viral infections such as Mononucleosis, Epstein-Barr Virus, or cytomegalovirus which may affect immunocompetence.\n* Active and overt parasitic, mycobacterial, or pyogenic infections that affect tests designated in Inclusion Criteria.\n\nConcurrent Medication:\n\nExcluded:\n\n* All drugs, medications and therapy not prescribed by the Principal Investigator, and not documented on the case report form (CRF).\n* Any drug, even aspirin, which is administered after vaccination and during the follow up periods which is not documented on the patient's CRF.\n\nPatients with the following are excluded:\n\n* Failure to meet any criteria listed under Inclusion Criteria.\n* Appearance of serologic or clinical evidence of HIV infection prior to vaccination.\n* Current evidence of clinically active viral infections.\n* Active and overt parasitic, mycobacterial, or pyogenic infections that affect tests designated in Inclusion Criteria.\n\nRisk Behavior:\n\nPatients who do not agree to behave sexually in a manner that will minimize the risk of HIV infection for the duration of the study are excluded.\n\nPatients must:\n\n* Be HIV seronegative.\n* Have excellent general health.\n* Be unable to bear children.\n* Have no immediate household contacts, sex partners, intimate contacts.\n* Be free of clinical skin diseases.\n* Have signed an informed consent.\n* Control subjects receiving Smallpox vaccine will also be selected under the same inclusion criteria. They may be recruited from low risk behavior populations; from laboratory and hospital employees providing service to the study who would normally require Smallpox vaccination; and may be heterosexual, homosexual, or bisexual.\n\nPatients must agree to behave sexually in a manner that will minimize the risk of HIV infection for the duration of the study."}, 'identificationModule': {'nctId': 'NCT00002261', 'briefTitle': 'A Comparative Phase I Clinical Study of HIVAC-1e and Smallpox (Vaccinia) Vaccines in Previously (Vaccinia) Vaccinated and Unvaccinated Volunteers', 'organization': {'class': 'INDUSTRY', 'fullName': 'Bristol-Myers Squibb'}, 'officialTitle': 'A Comparative Phase I Clinical Study of HIVAC-1e and Smallpox (Vaccinia) Vaccines in Previously (Vaccinia) Vaccinated and Unvaccinated Volunteers', 'orgStudyIdInfo': {'id': '063A'}, 'secondaryIdInfos': [{'id': 'AI452-003001'}]}, 'armsInterventionsModule': {'interventions': [{'name': 'Smallpox Vaccine', 'type': 'BIOLOGICAL'}, {'name': 'HIVAC-1e', 'type': 'BIOLOGICAL'}, {'name': 'gp160 Vaccine (MicroGeneSys)', 'type': 'BIOLOGICAL'}]}, 'contactsLocationsModule': {'locations': [{'zip': '064927600', 'city': 'Wallingford', 'state': 'Connecticut', 'country': 'United States', 'facility': 'Bristol - Myers Squibb Co', 'geoPoint': {'lat': 41.45704, 'lon': -72.82316}}], 'overallOfficials': [{'name': 'Bristol-Myers Squibb', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Bristol-Myers Squibb'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Bristol-Myers Squibb', 'class': 'INDUSTRY'}}}}