A Study in Healthy Subjects to Assess How Dosing of Rifampin Affects What the Body Does to a Dose of GW679769 (Casopitant).
Completed · Phase 1
Conditions studied: Nausea and Vomiting, Chemotherapy-Induced
In brief
This study will examine what the body does while taking GW679769 alone and together with rifampin in healthy adult subjects.
Key facts
- Study ID
- NCT00405080
- Run by
- GlaxoSmithKline
- People needed
- 12
- Starts
- 2006-11-11
- Expected to finish
- 2007-01-05
- Last updated by the study team
- 2017-09-12
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- healthy
- female subjects who cannot become pregnant
- able to swallow and keep down oral medication
- can understand and follow the protocol requirements and instructions
You may not qualify if…
- smokes at least 4 packs per day in the past 12 months
- use of prescription or non-prescription drug(s)
- herbal or dietary supplements or vitamins with 14 days prior to first dose of study medication
- a clinically relevant abnormality medical condition or circumstance making the subject unsuitable for the study per the study doctor
- blood donation in excess of 1 pint within 56 days before dosing of medication
- iron deficient
- history or drug allergy of study medication
- history of drug or alcohol abuse or dependency within the past 6 months
- subjects cannot use any nicotine-containing products within the last 6 months
- positive for HIV, Hepatitis B or C
- active peptic ulcer disease
- uncontrolled nausea and vomiting
- active infection
- heart failure
- female who is lactating
- female who has a positive pregnancy test
Where it is running
- GSK Investigational Site — Tacoma, Washington, United States
Full record on ClinicalTrials.gov
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