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CLINICAL_TRIALS ClinicalTrials.gov record update

Phase 2a Double-Blind, Randomized, Parallel Group, Dose-Ranging Study to Assess the Safety and Efficacy of Three Doses of TVGV-1 Vaccine Compared to Its Adjuvant, GPI-0100, in Subjects With Histologically Confirmed HPV Induced Cervical HSIL

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT02576561
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:36:46.650791+00:00
Published At
2017-10-25T00:00:00+00:00
Record Updated At
2017-10-25
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
["Human Papillomavirus", "High-Grade Squamous Intraepithelial Lesions"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2017-10-25"
protocolSection.identificationModule.nctId
"NCT02576561"
protocolSection.identificationModule.officialTitle
"Phase 2a Double-Blind, Randomized, Parallel Group, Dose-Ranging Study to Assess the Safety and Efficacy of Three Doses of TVGV-1 Vaccine Compared to Its Adjuvant, GPI-0100, in Subjects With Histologically Confirmed HPV Induced Cervical HSIL"
protocolSection.statusModule.overallStatus
"UNKNOWN"
protocolSection.designModule.phases
["PHASE2"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Human Papillomavirus (protocolSection.conditionsModule.conditions)
  • High-Grade Squamous Intraepithelial Lesions (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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