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CLINICAL_TRIALS ClinicalTrials.gov record update

A Prospective, Observational, Long-Term Follow-Up (LTFU) Study to Evaluate the Long-Term Safety of the Krystal Biotech, Inc. Gene Therapy Backbone Products Using HSV-1 Backbone

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04917887
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:38:08.934186+00:00
Published At
2021-06-08T00:00:00+00:00
Record Updated At
2021-06-08
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
["Dystrophic Epidermolysis Bullosa", "Recessive Dystrophic Epidermolysis Bullosa", "Dominant Dystrophic Epidermolysis Bullosa"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2021-06-08"
protocolSection.identificationModule.nctId
"NCT04917887"
protocolSection.identificationModule.officialTitle
"A Prospective, Observational, Long-Term Follow-Up (LTFU) Study to Evaluate the Long-Term Safety of the Krystal Biotech, Inc. Gene Therapy Backbone Products Using HSV-1 Backbone"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Dystrophic Epidermolysis Bullosa (protocolSection.conditionsModule.conditions)
  • Recessive Dystrophic Epidermolysis Bullosa (protocolSection.conditionsModule.conditions)
  • Dominant Dystrophic Epidermolysis Bullosa (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.