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CompletedNCT01381341

To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib.

A Phase 1 Pharmacokinetic Study To Compare the Relative Bioavailability of Two Clinical Formulations of Linifanib in Subjects With Solid Tumors

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Abbott · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A pharmacokinetic study to compare 2 clinical formulations of linifanib.

Detailed description

This study is designed to evaluate the bioavailability of linifanib from 2 formulations. Subjects may enroll in a separate extension study to continue receiving linifanib after completion of this study.

Conditions

Interventions

TypeNameDescription
DRUGlinifanibQD on Day 1 of Periods 1 and 2

Timeline

Start date
2011-05-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2011-06-27
Last updated
2012-03-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01381341. Inclusion in this directory is not an endorsement.

To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. (NCT01381341) · Clinical Trials Directory