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A Phase III Multicenter, Double-Blind, Crossover Design Study to Evaluate Lipid-Altering Efficacy and Safety of Extended-Release Niacin/Laropiprant/Simvastatin Combination Tablet in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01294683
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:36:50.385429+00:00
Published At
2016-12-13T00:00:00+00:00
Record Updated At
2018-08-16
Results Posted At
2016-12-13
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
["Primary Hypercholesterolemia", "Dyslipidemia"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2018-08-16"
protocolSection.identificationModule.nctId
"NCT01294683"
protocolSection.identificationModule.officialTitle
"A Phase III Multicenter, Double-Blind, Crossover Design Study to Evaluate Lipid-Altering Efficacy and Safety of Extended-Release Niacin/Laropiprant/Simvastatin Combination Tablet in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia"
protocolSection.statusModule.overallStatus
"TERMINATED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2016-12-13"

Study condition terms

  • Primary Hypercholesterolemia (protocolSection.conditionsModule.conditions)
  • Dyslipidemia (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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