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A Phase I Single-Dose Open-Label Study Determining The Absolute Bioavailability Of Oral Rolapitant By Using An Intravenous Microdose Of [14C]-Rolapitant In Healthy Volunteers: Absolute Bioavailability Study.

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Trial Profile

A Phase I Single-Dose Open-Label Study Determining The Absolute Bioavailability Of Oral Rolapitant By Using An Intravenous Microdose Of [14C]-Rolapitant In Healthy Volunteers: Absolute Bioavailability Study.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 10 Feb 2017

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At a glance

  • Drugs Rolapitant (Primary) ; Rolapitant (Primary)
  • Indications Chemotherapy-induced nausea and vomiting
  • Focus Pharmacokinetics
  • Sponsors TESARO

Most Recent Events

  • 10 Feb 2017 New trial record
  • 31 Jan 2017 Results published in the Clinical Pharmacology and Therapeutics journal.

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