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CLINICAL_TRIALS ClinicalTrials.gov record update

A Double-Masked, Randomized, Controlled, Multiple-Dose Study to Evaluate the Efficacy, Safety and Tolerability of QR-421a in Subjects With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Gene With Early to Moderate Vision Loss

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05176717
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:26:18.525306+00:00
Published At
2023-01-20T00:00:00+00:00
Record Updated At
2024-08-07
Results Posted At
2023-01-20
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
["Retinitis Pigmentosa", "Usher Syndrome Type 2", "Deaf Blind", "Retinal Disease", "Eye Diseases", "Eye Diseases, Hereditary", "Eye Disorders Congenital", "Vision Disorders"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-08-07"
protocolSection.identificationModule.nctId
"NCT05176717"
protocolSection.identificationModule.officialTitle
"A Double-Masked, Randomized, Controlled, Multiple-Dose Study to Evaluate the Efficacy, Safety and Tolerability of QR-421a in Subjects With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Gene With Early to Moderate Vision Loss"
protocolSection.statusModule.overallStatus
"TERMINATED"
protocolSection.designModule.phases
["PHASE2", "PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2023-01-20"

Study condition terms

  • Retinitis Pigmentosa (protocolSection.conditionsModule.conditions)
  • Usher Syndrome Type 2 (protocolSection.conditionsModule.conditions)
  • Deaf Blind (protocolSection.conditionsModule.conditions)
  • Retinal Disease (protocolSection.conditionsModule.conditions)
  • Eye Diseases (protocolSection.conditionsModule.conditions)
  • Eye Diseases, Hereditary (protocolSection.conditionsModule.conditions)
  • Eye Disorders Congenital (protocolSection.conditionsModule.conditions)
  • Vision Disorders (protocolSection.conditionsModule.conditions)

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

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.