Trials / Completed
CompletedNCT01080365
Study Comparing Two Different Tablet Formulations Of Bosutinib Under Fed Conditions
A Single Dose Bioequivalence Study Comparing The Commercial Tablet Formulation To The Clinical Tablet Of Bosutinib In Healthy Subjects
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 31 (actual)
- Sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer · Industry
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Accepted
Summary
Study comparing 2 formulations of bosutinib in healthy subjects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | SKI-606 (Bosutinib) | 500 mg commercial formulation film coated tablet, administered once daily |
| DRUG | SKI-606 (Bosutinib) | 500 mg (5 ×100 mg) phase 3 formulation film coated tablets, administered orally once daily |
Timeline
- Start date
- 2010-02-01
- Primary completion
- 2010-03-01
- Completion
- 2010-03-01
- First posted
- 2010-03-04
- Last updated
- 2010-09-06
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01080365. Inclusion in this directory is not an endorsement.