Clinical Trials Directory

Trials / Completed

CompletedNCT00435669

A Phase I Study to Determine Absorption, Distribution, Metabolism, and Elimination of a Single Radiolabeled Dose of Brivanib (BMS-582664)

Mass Balance, Pharmacokinetics and Metabolism of [14C]BMS-582664 Prodrug of BMS-540215, in Subjects With Advanced or Metastatic Solid Tumors

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
4 (actual)
Sponsor
Bristol-Myers Squibb · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this trial is to determine the mass balance, pharmacokinetics, metabolism, and routes and extent of elimination of BMS-582664

Conditions

Interventions

TypeNameDescription
DRUGBrivanibOral Solution, Oral, 800 mg, X1 on Day 1, 10 D for ADME
DRUGBrivanibTablet, Oral, Brivanib 800 mg, QD, until progression

Timeline

Start date
2007-09-01
Primary completion
2008-06-01
Completion
2008-06-01
First posted
2007-02-15
Last updated
2009-01-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00435669. Inclusion in this directory is not an endorsement.