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CompletedNCT02089295

Dose Proportionality Study Of PF-00345439 Formulation Under Fed Conditions

An Open-label, Randomized, Single-dose, Three-way Crossover Study to Evaluate the Dose Proportionality of 5 Mg, 20 Mg and 40 Mg of PF-00345439 Formulation K Under Intermediate-fat Fed Conditions in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Pain Therapeutics · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

To evaluate the dose proportionality of 5 mg, 20 mg and 40 mg of PF 00345439 formulation under fed conditions in healthy volunteers.

Conditions

Interventions

TypeNameDescription
DRUGOxycodoneOne capsule of 5 mg PF-00345439 Formulation K, single dose, under fed conditions
DRUGOxycodoneOne capsule of 20 mg PF-00345439 Formulation K, single dose, under fed conditions
DRUGOxycodoneOne capsule of 40 mg PF-00345439 Formulation K, single dose, under fed conditions

Timeline

Start date
2014-04-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2014-03-17
Last updated
2016-04-04

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02089295. Inclusion in this directory is not an endorsement.

Dose Proportionality Study Of PF-00345439 Formulation Under Fed Conditions (NCT02089295) · Clinical Trials Directory