Trials / Completed
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
| Type | Name | Description |
|---|---|---|
| DRUG | Oxycodone | One capsule of 5 mg PF-00345439 Formulation K, single dose, under fed conditions |
| DRUG | Oxycodone | One capsule of 20 mg PF-00345439 Formulation K, single dose, under fed conditions |
| DRUG | Oxycodone | One 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.