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An Open-Label Multicenter Study to Evaluate the Safety, Tolerability and Pharmacokinetics of SBC-102 in Adult Participants With Liver Dysfunction Due to Lysosomal Acid Lipase Deficiency

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01307098
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:37:04.019052+00:00
Published At
2018-12-11T00:00:00+00:00
Record Updated At
2018-12-11
Results Posted At
2018-12-11
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
["Cholesterol Ester Storage Disease(CESD)", "Lysosomal Acid Lipase Deficiency", "LAL-Deficiency"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2018-12-11"
protocolSection.identificationModule.nctId
"NCT01307098"
protocolSection.identificationModule.officialTitle
"An Open-Label Multicenter Study to Evaluate the Safety, Tolerability and Pharmacokinetics of SBC-102 in Adult Participants With Liver Dysfunction Due to Lysosomal Acid Lipase Deficiency"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE1", "PHASE2"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2018-12-11"

Study condition terms

  • Cholesterol Ester Storage Disease(CESD) (protocolSection.conditionsModule.conditions)
  • Lysosomal Acid Lipase Deficiency (protocolSection.conditionsModule.conditions)
  • LAL-Deficiency (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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