Ignite Creation Date:
2025-12-24 @ 1:49 PM
Ignite Modification Date:
2025-12-31 @ 4:24 AM
Study NCT ID:
NCT00981695
Status:
UNKNOWN
Last Update Posted:
2011-06-16
First Post:
2009-09-21
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Safety and Immunogenicity Study of Candidate HIV-1 Vaccine Given to Healthy Infants Born to HIV-1-infected Mothers
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D015658', 'term': 'HIV Infections'}], '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'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1', 'PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['OUTCOMES_ASSESSOR']}, 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 72}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2009-11'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2009-09', 'completionDateStruct': {'date': '2011-10', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2011-06-15', 'studyFirstSubmitDate': '2009-09-21', 'studyFirstSubmitQcDate': '2009-09-21', 'lastUpdatePostDateStruct': {'date': '2011-06-16', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2009-09-22', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2011-07', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'For safety and reactogenicity: Actively and passively collected data on adverse events.', 'timeFrame': 'Up to 28 weeks after vaccination'}], 'secondaryOutcomes': [{'measure': 'For immunogenicity to KEPI vaccines: Antibody levels to specific vaccines as measured by ELISA.', 'timeFrame': '1 week before and 1 week after vaccination'}, {'measure': 'For immunogenicity to MVA.HIVA: Frequency of IFN-γ-producing cells determined in an ELISPOT assay after overnight stimulation with a pool of HIVA-derived peptides.', 'timeFrame': 'Up to 24 weeks after vaccination'}]}, 'oversightModule': {'oversightHasDmc': True}, 'conditionsModule': {'keywords': ['HIV', 'Vaccine', 'MVA', 'PMTCT', 'HIV preventive vaccine', 'HIV seronegativity'], 'conditions': ['HIV-1', 'HIV Infections']}, 'referencesModule': {'references': [{'pmid': '25173484', 'type': 'DERIVED', 'citation': 'Njuguna IN, Ambler G, Reilly M, Ondondo B, Kanyugo M, Lohman-Payne B, Gichuhi C, Borthwick N, Black A, Mehedi SR, Sun J, Maleche-Obimbo E, Chohan B, John-Stewart GC, Jaoko W, Hanke T. PedVacc 002: a phase I/II randomized clinical trial of MVA.HIVA vaccine administered to infants born to human immunodeficiency virus type 1-positive mothers in Nairobi. Vaccine. 2014 Oct 7;32(44):5801-8. doi: 10.1016/j.vaccine.2014.08.034. Epub 2014 Aug 27.'}]}, 'descriptionModule': {'briefSummary': 'Objectives:\n\nPrimary: Safety and immunogenicity of MVA.HIVA vaccine in 20-week-old healthy Kenyan infants born to HIV-1-infected mothers.\n\nSecondary:\n\n* HIV-1 immunogenicity comparison between MVA.HIVA and age-matched unvaccinated control arms in each cohort (breastfeeding or formula feeding)\n* HIV-1 immunogenicity comparison between breastfeeding and formula feeding infants receiving MVA.HIVA\n* HIV-1 immunogenicity comparison between breastfeeding and formula feeding infants in the age-matched unvaccinated control group\n* Comparison of responses to certain Kenyan Extended Programme on Immunization (KEPI) vaccines (OPV, DTP, HBV, and HiB) between MVA.HIVA versus age-matched unvaccinated controls in each cohort, between breast versus formula feeding infants in the age-matched unvaccinated control group, and between breast versus formula infants receiving MVA.HIVA\n* Comparison of immune activation and phenotypic profile of lymphocytes between breast and formula feeding infants in each cohort (MVA.HIVA and age-matched unvaccinated control)\n* Build capacity for Infant HIV-1 Vaccine Clinical Trials Centre in Nairobi, Kenya.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD'], 'maximumAge': '3 Days', 'healthyVolunteers': False, 'eligibilityCriteria': "Infant Inclusion Criteria\n\n* Healthy infants\n* \\< 3 days of age (day of birth = Day 0) at enrolment\n* Birth weight \\> 2500 grams\n* Born to an eligible woman\n* Written informed consent by parent\n\nInfant Exclusion Criteria\n\n* HIV infection, as determined by a filter paper and/or RNA test prior to vaccination.\n* Participation in any other HIV-1 vaccine or drug trial.\n* Failure to receive all standard KEPI immunizations according to national immunization programme.\n* Weight for age z-scores outside of 2 standard deviations of normal at the time of vaccination.\n* Acute disease at the time of vaccination (acute disease is defined as the presence of a moderate or severe illness with or without fever). All vaccines can be administered to persons with a minor illness such as diarrhoea, mild upper respiratory tract infection with or without low-grade febrile illness, i.e., temperature of \\<37.5 °C).\n* Axillary temperature of ≥ 37.5 °C at the time of vaccination.\n* Any clinically significant abnormal finding on screening from biochemistry or haematology by the time of vaccination.\n* History of allergic disease or reactions likely to be exacerbated by any component of the vaccine, e.g., egg products.\n* Presence of any underlying disease that compromises the diagnosis and evaluation of response to the vaccine.\n* Any other on-going chronic illness requiring hospital specialist supervision.\n* Administration of immunoglobulins and/or any blood products within one month preceding the planned administration of the vaccine candidate.\n* Any history of anaphylaxis in reaction to vaccination.\n* Research Physician's assessment of lack of willingness by parents to participate and comply with all requirements of the protocol, or identification of any factor felt to significantly increase the infant's risk of suffering an adverse outcome.\n* Likelihood of travel away from the study area."}, 'identificationModule': {'nctId': 'NCT00981695', 'acronym': 'PedVacc002', 'briefTitle': 'Safety and Immunogenicity Study of Candidate HIV-1 Vaccine Given to Healthy Infants Born to HIV-1-infected Mothers', 'organization': {'class': 'OTHER_GOV', 'fullName': 'Medical Research Council'}, 'officialTitle': 'An Open Randomized Phase I/II Study Evaluating Safety and Immunogenicity of a Candidate HIV-1 Vaccine, MVA.HIVA, Administered to Healthy Infants Born to HIV-1-infected Mothers', 'orgStudyIdInfo': {'id': 'PV002'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Vaccinees', 'description': '18 breast-fed and 18 formula-fed infants at the age of 20 weeks', 'interventionNames': ['Biological: MVA.HIVA']}, {'type': 'NO_INTERVENTION', 'label': 'Controls', 'description': '18 breast-fed and 18 formula-fed infants at the age of 20 weeks'}], 'interventions': [{'name': 'MVA.HIVA', 'type': 'BIOLOGICAL', 'description': '1 dose of 5 x 10\\^7 pfu of MVA.HIVA administered intramuscularly', 'armGroupLabels': ['Vaccinees']}]}, 'contactsLocationsModule': {'locations': [{'city': 'Nairobi', 'status': 'RECRUITING', 'country': 'Kenya', 'contacts': [{'name': 'Walter Jaoko', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Kenyatta National Hospital', 'geoPoint': {'lat': -1.28333, 'lon': 36.81667}}], 'centralContacts': [{'name': 'Walter Jaoko, MB MTMed PhD', 'role': 'CONTACT', 'email': 'Wjaoko@kaviuon.org', 'phone': '+254-02-2717694'}], 'overallOfficials': [{'name': 'Tomas Hanke', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Medical Research Council'}, {'name': 'Walter Jaoko', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of Nairobi'}, {'name': 'Grace John-Stewart', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of Washington'}, {'name': 'Marie Reilly', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Karolinska Institutet'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Medical Research Council', 'class': 'OTHER_GOV'}, 'collaborators': [{'name': 'European and Developing Countries Clinical Trials Partnership (EDCTP)', 'class': 'OTHER_GOV'}], 'responsibleParty': {'oldNameTitle': 'Tomas Hanke', 'oldOrganization': 'Medical Research Council, UK'}}}}