Clinical Trials Directory

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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

TypeNameDescription
DRUGSKI-606 (Bosutinib)500 mg commercial formulation film coated tablet, administered once daily
DRUGSKI-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.

Study Comparing Two Different Tablet Formulations Of Bosutinib Under Fed Conditions (NCT01080365) · Clinical Trials Directory