Pharmacokinetics And Relative Bioavailability Study Of Oxycodone in Healthy Volunteers
Completed · Phase 1
Conditions studied: Healthy
In brief
To estimate the pharmacokinetics and relative bioavailability of oxycodone after administration of 40 mg doses of PF-00345439 formulations taken whole under fed conditions and after chewing under fasted conditions in healthy volunteers
Key facts
- Study ID
- NCT01717027
- Run by
- Pain Therapeutics
- People needed
- 19
- Starts
- 2012-11-01
- Expected to finish
- 2013-01-01
- Last updated by the study team
- 2015-08-31
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy male and/or female subjects between 18 and 55 years of age (inclusive).
You may not qualify if…
- Evidence or history of clinically significant disease.
- Positive urine drug test
Where it is running
- Pfizer Investigational Site — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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