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A multicenter, randomized, double-blind, parallel group, 12 week study to evaluate the efficacy and safety of extended-release (ER) niacin/laropiprant in patients with primary hypercholesterolemia or mixed dyslipidemia

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Trial Profile

A multicenter, randomized, double-blind, parallel group, 12 week study to evaluate the efficacy and safety of extended-release (ER) niacin/laropiprant in patients with primary hypercholesterolemia or mixed dyslipidemia

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 06 May 2022

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At a glance

  • Drugs Niacin/laropiprant (Primary) ; Atorvastatin; Simvastatin
  • Indications Dyslipidaemias; Hypercholesterolaemia
  • Focus Registrational; Therapeutic Use
  • Sponsors Merck & Co; Merck Sharp & Dohme; Merck Sharp & Dohme Corp.

    • Most Recent Events

    • 15 Jun 2019 This trial has been completed in France, according to European Clinical Trials Database.
    • 16 Jul 2008 Actual patient number added (1250) as reported by ClinicalTrials.gov.
    • 16 Jul 2008 Actual end date added (Jul 2008) as reported by ClinicalTrials.gov.

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