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CLINICAL_TRIALS ClinicalTrials.gov record update

A Double-Masked, Randomized, Placebo-Controlled, Paired-Eye Study to Evaluate the Efficacy, Safety and Tolerability of Sepofarsen in Subjects With Leber Congenital Amaurosis (LCA) Due to the c.2991+1655A>G (p.Cys998X) Mutation in the CEP290 Gene

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT06891443
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:28:12.759040+00:00
Published At
2026-03-17T00:00:00+00:00
Record Updated At
2026-03-17
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
["Leber Congenital Amaurosis 10", "Blindness", "Leber Congenital Amaurosis", "Sensation Disorders", "Vision Disorder", "Neurological Manifestations", "Eye Diseases, Hereditary", "Eye Diseases", "Eye Disorders Congenital", "Retinal Disease"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2026-03-17"
protocolSection.identificationModule.nctId
"NCT06891443"
protocolSection.identificationModule.officialTitle
"A Double-Masked, Randomized, Placebo-Controlled, Paired-Eye Study to Evaluate the Efficacy, Safety and Tolerability of Sepofarsen in Subjects With Leber Congenital Amaurosis (LCA) Due to the c.2991+1655A\u003eG (p.Cys998X) Mutation in the CEP290 Gene"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Leber Congenital Amaurosis 10 (protocolSection.conditionsModule.conditions)
  • Blindness (protocolSection.conditionsModule.conditions)
  • Leber Congenital Amaurosis (protocolSection.conditionsModule.conditions)
  • Sensation Disorders (protocolSection.conditionsModule.conditions)
  • Vision Disorder (protocolSection.conditionsModule.conditions)
  • Neurological Manifestations (protocolSection.conditionsModule.conditions)
  • Eye Diseases, Hereditary (protocolSection.conditionsModule.conditions)
  • Eye Diseases (protocolSection.conditionsModule.conditions)
  • Eye Disorders Congenital (protocolSection.conditionsModule.conditions)
  • Retinal Disease (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.