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An Open-Label, Single-Dose, Randomized, Two-Period, Crossover Study Evaluating the Absolute Bioavailability of Brincidofovir Administered as CMX001-P-SUS-HPI-010 Suspension Formulation Compared to CMX001-P-IVS-PPS-003 BCV Intravenous formulation in Healthy Japanese and Non-Japanese Adult Subjects

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Trial Profile

An Open-Label, Single-Dose, Randomized, Two-Period, Crossover Study Evaluating the Absolute Bioavailability of Brincidofovir Administered as CMX001-P-SUS-HPI-010 Suspension Formulation Compared to CMX001-P-IVS-PPS-003 BCV Intravenous formulation in Healthy Japanese and Non-Japanese Adult Subjects

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 02 Jul 2019

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At a glance

  • Drugs Brincidofovir (Primary) ; Brincidofovir (Primary)
  • Indications Adenovirus infections; Cytomegalovirus infections; Monkeypox; Smallpox; Viral infections
  • Focus Pharmacokinetics
  • Sponsors Chimerix

Most Recent Events

  • 09 May 2019 Status changed from not yet recruiting to discontinued, according to a Chimerix media release.
  • 20 Dec 2018 The anticipated date of last patient enrollment is 29/03/2019.
  • 20 Dec 2018 New trial record

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