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Open-Label, Multiple-Dose, Dose Escalation Study to Evaluate the Pharmacodynamics, Pharmacokinetics, and Safety of Coadministration of BMS-650032, BMS-790052, and BMS-791325 When Administered for 24 or 12 Weeks in Treatment-Naive Subjects Infected With Hepatitis C Virus Genotype 1.

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Trial Profile

Open-Label, Multiple-Dose, Dose Escalation Study to Evaluate the Pharmacodynamics, Pharmacokinetics, and Safety of Coadministration of BMS-650032, BMS-790052, and BMS-791325 When Administered for 24 or 12 Weeks in Treatment-Naive Subjects Infected With Hepatitis C Virus Genotype 1.

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 07 Nov 2021

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At a glance

  • Drugs Asunaprevir (Primary) ; Asunaprevir/becabluvir/daclatasvir (Primary) ; Beclabuvir (Primary) ; Daclatasvir (Primary)
  • Indications Hepatitis C
  • Focus Therapeutic Use
  • Sponsors Bristol-Myers Squibb

    • Most Recent Events

    • 10 Sep 2015 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
    • 24 Mar 2014 Results from patients with genotype 4 hepatitis C will be presented at The International Liver Congress, the 49th annual meeting of the European Association for the Study of the Liver (EASL) according to a Bristol-Myers Squibb media release.
    • 06 Mar 2014 Interim results in genotype 1 patients (n=166) presented at the 21st Conference on Retroviruses and Opportunistic Infections.

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