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CLINICAL_TRIALS ClinicalTrials.gov record update

A Phase 2/3, Randomized, Double-blinded , Parallel Controlled Trial to Evaluate the Immunogenicity, Safety and Efficacy of A Heterologous Booster Dose With COVID-19 mRNA Vaccines (Bivalent) , in Previously Vaccinated Subjects Against COVID-19 With 2/3 Doses COVID-19 Vaccine Compared to a Booster Dose With mRNA COVID-19 Vaccine(Pfizer Bivalent Vaccine)in Adults.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05911087
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:39:06.725881+00:00
Published At
2023-06-20T00:00:00+00:00
Record Updated At
2023-06-20
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Immunogenicity", "Safety"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2023-06-20"
protocolSection.identificationModule.nctId
"NCT05911087"
protocolSection.identificationModule.officialTitle
"A Phase 2/3, Randomized, Double-blinded , Parallel Controlled Trial to Evaluate the Immunogenicity, Safety and Efficacy of A Heterologous Booster Dose With COVID-19 mRNA Vaccines (Bivalent) , in Previously Vaccinated Subjects Against COVID-19 With 2/3 Doses COVID-19 Vaccine Compared to a Booster Dose With mRNA COVID-19 Vaccine\uff08Pfizer Bivalent Vaccine\uff09in Adults."
protocolSection.statusModule.overallStatus
"UNKNOWN"
protocolSection.designModule.phases
["PHASE2", "PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Immunogenicity (protocolSection.conditionsModule.conditions)
  • Safety (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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