CLINICAL_TRIALS ClinicalTrials.gov record update

Characterization of Two Novel Truncating Mutations in the Apob Gene Leading to Hypobetalipoproteinemia: A Pilot Study

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT03963037
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:37:48.866832+00:00
Published At: 2020-02-20T00:00:00+00:00
Record Updated At: 2020-02-20
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Familial Hypobetalipoproteinaemia - Heterozygous Form", "Low-LDL-syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2020-02-20"
protocolSection.identificationModule.nctId: "NCT03963037"
protocolSection.identificationModule.officialTitle: "Characterization of Two Novel Truncating Mutations in the Apob Gene Leading to Hypobetalipoproteinemia: A Pilot Study"
protocolSection.statusModule.overallStatus: "UNKNOWN"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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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