CLINICAL_TRIALS ClinicalTrials.gov record update

Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT01668186
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-25T22:28:51.046045+00:00
Published At: 2025-12-10T00:00:00+00:00
Record Updated At: 2025-12-10
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: ["Peroxisome Biogenesis Disorder", "Zellweger Spectrum Disorder", "RCDP - Rhizomelic Chondrodysplasia Punctata", "D-Bifunctional Protein Deficiency", "Alpha-Methylacyl-CoA Racemase Deficiency", "Peroxisomal Acyl-CoA Oxidase Deficiency", "Peroxisomal Acyl-CoA Oxidase 2 Deficiency", "ATP Binding Cassette Subfamily D Member 3 Gene Mutation", "ACBD5 (AcylCoA Binding Domain 5) Deficiency", "Adult Refsum Disease", "Sterol Carrier Protein 2 Deficiency"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2025-12-10"
protocolSection.identificationModule.nctId: "NCT01668186"
protocolSection.identificationModule.officialTitle: "Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)"
protocolSection.statusModule.overallStatus: "RECRUITING"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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