CLINICAL_TRIALS ClinicalTrials.gov record update

A Phase 1, Open-Label, Parallel-Group Study to Evaluate the Pharmacokinetics, Safety and Tolerability of a Single Oral Dose of 5 mg Vortioxetine in Subjects With Normal Hepatic Function or Severe Hepatic Impairment

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT02170220
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:36:02.102570+00:00
Published At: 2016-01-05T00:00:00+00:00
Record Updated At: 2016-01-05
Results Posted At: 2016-01-05
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: ["Severe Hepatic Impairment"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2016-01-05"
protocolSection.identificationModule.nctId: "NCT02170220"
protocolSection.identificationModule.officialTitle: "A Phase 1, Open-Label, Parallel-Group Study to Evaluate the Pharmacokinetics, Safety and Tolerability of a Single Oral Dose of 5 mg Vortioxetine in Subjects With Normal Hepatic Function or Severe Hepatic Impairment"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2016-01-05"

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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