[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100307362":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":24,"centralContacts":10,"locations":28,"responsibleParty":50,"collaborators":10,"id":52,"slug":53,"hasResults":54,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":10,"eligibilityCriteria":58,"healthyVolunteers":54,"sex":59,"minAge":60,"maxAge":61,"enrollmentInfo":62,"targetDuration":10,"studyType":65,"phases":10,"briefSummary":66,"conditions":67,"keywords":69,"overallStatus":77,"whyStopped":10,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"GlaxoSmithKline","INDUSTRY",[8,12,15,18,21],{"label":9,"type":10,"description":11,"interventionNames":10},"R012-20 Group",null,"Participants received a full dose of RTS,S\u002FAS01E at Month 0, Month 1, Month 2 and Month 20 of study NCT03276962.",{"label":13,"type":10,"description":14,"interventionNames":10},"R012-14-mD Group","Participants received a full dose of RTS,S\u002FAS01E at Month 0, Month 1, Month 2, Month 14, Month 26 and Month 38 of study NCT03276962.",{"label":16,"type":10,"description":17,"interventionNames":10},"Fx012-14-mFxD Group","Participants received a full dose of RTS,S\u002FAS01E at Month 0 and Month 1, and RTS,S\u002FAS01E 1\u002F5th dose at Month 2, Month 14, Month 26 and Month 38 of study NCT03276962.",{"label":19,"type":10,"description":20,"interventionNames":10},"Fx017-mFxD Group","Participants received a full dose of RTS,S\u002FAS01E at Month 0 and Month 1, and RTS,S\u002FAS01E 1\u002F5th dose at Month 7, Month 20 and Month 32 of study NCT03276962.",{"label":22,"type":10,"description":23,"interventionNames":10},"Control Group","Participants received rabies vaccine at Month 0, Month 1 and Month 2 of study NCT03276962.",[25],{"name":26,"affiliation":5,"role":27},"GSK Clinical Trials","STUDY_DIRECTOR",[29,40],{"facility":30,"status":10,"city":31,"state":10,"zip":10,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":10},"GSK Investigational Site","Kumasi","Ghana","GH",{"type":35,"coordinates":36},"Point",[37,38],-1.62443,6.68848,{"lat":38,"lon":37},{"facility":30,"status":10,"city":41,"state":10,"zip":42,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":49,"contacts":10},"Kisumu","40100","Kenya","KE",{"type":35,"coordinates":46},[47,48],34.76171,-0.10221,{"lat":48,"lon":47},{"type":51,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100307362","study-to-assess-the-vaccine-efficacy-against-malaria-infection-in-children-immunized-with-the-primary-and-yearly-booster-of-the-rtssas01e-vaccine-as-part-of-their-participation-in-the-malaria-094-204889nct03276962-study-100307362",true,"NCT03281291","Study to Assess the Vaccine Efficacy Against Malaria Infection, in Children Immunized With the Primary and Yearly Booster of the RTS,S\u002FAS01E Vaccine, as Part of Their Participation in the Malaria-094 (204889\u002FNCT03276962) Study.","Molecular Detection and Genotyping of Plasmodium Falciparum Parasites in Young African Children After Immunization With RTS,S\u002FAS01E Malaria Vaccine. An Ancillary Study Protocol to GlaxoSmithKline Phase IIb RTS,S\u002FAS01E Malaria Vaccine Trial (Study Number 204889) Entitled, \"Efficacy, Safety and Immunogenicity Study of GSK Biologicals' Candidate Malaria Vaccine (SB257049) Evaluating Schedules With or Without Fractional Doses, Early Dose 4 and Yearly Doses, in Children 5-17 Months of Age.","Inclusion Criteria:\n\n* Participants' parent(s)\u002FLAR(s) who, in the opinion of the investigator, complied with the requirements of the protocol (e.g. return for follow-up visits).\n* Signed or thumb-printed and witnessed informed consent obtained from the parent(s)\u002FLAR(s) of the participant prior to performance of any study specific procedure. Where parent(s)\u002FLAR(s) were illiterate, the consent form was countersigned by an independent witness.\n* A male or female between, and including, five and 17 months of age at the time of the first vaccination.\n* Healthy participants as established by medical history and clinical examination before entering into the study.\n* Previously received three documented doses of diphtheria, tetanus, pertussis, hepatitis B vaccine (DTPHepB), and at least three doses of oral polio vaccine.\n\nExclusion Criteria:\n\n* Child in care.\n* Use of a drug or vaccine that is not approved for that indication (by one of the following regulatory authorities: Food and Drug Administration \\[FDA; USA\\] or European Union member state or WHO \\[with respect to prequalification\\]) other than the study vaccines during the period starting 30 days before the first dose of study vaccines (Day -29 to Day 0), or planned use during the study period.\n* Any medical condition that in the judgment of the investigator would have made the intramuscular injection unsafe.\n\nChronic administration (defined as more than 14 days in total) of immunosuppressants or other immune-modifying drugs during the period starting six months prior to the first vaccine dose. For corticosteroids, this meant prednisone (0.5 mg\u002Fkg\u002Fday (for pediatric participants) or equivalent. Inhaled and topical steroids are allowed.\n\n* Planned administration\u002Fadministration of a vaccine not foreseen by the study protocol in the period starting seven days before each dose and ending seven days after each dose of vaccine administration.\n* Concurrently participating in another clinical study, at any time during the study period, in which the participant has been or was to be exposed to an investigational or a non-investigational vaccine\u002Fproduct (pharmaceutical product or device).\n* Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination (no laboratory testing required).\n* Family history of congenital or hereditary immunodeficiency.\n* History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccines.\n* History of anaphylaxis post-vaccination.\n* History of any, or documented, serious adverse reaction to rabies vaccination.\n* Contraindication to rabies vaccination (Rabipur is contraindicated in participants with a history of a severe hypersensitivity to any of the ingredients in the vaccine. Note that the vaccine contains polygeline and residues of chicken proteins, and may contain traces of neomycin, chlortetracycline and amphotericin B).\n* Major congenital defects.\n* Serious chronic illness.\n* Children with a past history of a neurological disorder or atypical febrile seizure (a febrile seizure is atypical if it meets one of the following criteria: not associated with fever; lasts \\> 5 minutes; focal (not generalized); followed by transient or persistent neurological abnormality; occurs in a child \\\u003C 6 months of age).\n* Acute disease and\u002For fever at the time of enrolment.\n* Fever is defined as temperature ≥ 37.5°C\u002F99.5°F for oral, axillary or tympanic route, or ≥ 38.0°C\u002F100.4°F for rectal route.\n* Participants with a minor illness (such as mild diarrhea, mild upper respiratory infection) without fever may have been enrolled at the discretion of the investigator.\n* Administration of immunoglobulins and\u002For any blood products during the period starting three months before the first dose of study vaccine or planned administration during the study period.\n* Moderate or severe malnutrition at screening defined as weight for age or weight for height Z-score \\\u003C -2.\n* Hemoglobin concentration \\\u003C 8 g\u002Fdl at screening.\n* Same sex twins (to avoid misidentification).\n* Maternal death.\n* Prior receipt of an investigational malaria vaccine.","ALL","5 Months","17 Months",{"count":63,"type":64},1500,"ACTUAL","OBSERVATIONAL","The aim of this study was to evaluate the effectiveness of the RTS,S\u002FAS01E malaria vaccine against both clinical and asymptomatic malaria infections by detecting Plasmodium falciparum (P. falciparum) parasites in blood samples collected from children who received the primary and yearly booster doses of the RTS,S\u002FAS01E vaccine, as part of their participation in the Malaria-094 parent clinical study. The genomic analysis was conducted on parasites found in blood spot samples from children aged 5-17 months, who were vaccinated according to different dosage and schedule regimens as part of the Malaria-094 parent clinical study.",[68],"Malaria",[70,71,72,73,74,75,76],"malaria vaccine","infants","malaria","RTS,S\u002FAS01","falciparum","genomics","efficacy","COMPLETED","2024-12-03",{"date":80,"type":64},"2025-01-23",{"date":82,"type":64},"2018-11-19",{"date":84,"type":64},"2023-10-23",{"name":5,"class":6},2]