Effect of Ketoconazole on the Pharmacokinetics of Vinflunine - Full Text View

Purpose

The purpose of the study is to test how ketoconazole affects with handling of vinflunine by the body which might affect how much vinflunine is in the blood stream and for how long

Condition	Intervention	Phase
Cancer	Drug: vinflunine + ketaconazole	Phase I

MedlinePlus related topics:

Cancer

ChemIDplus related topics:

Ketoconazole Vinflunine

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment, Non-Randomized, Open Label, Active Control, Parallel Assignment, Pharmacokinetics Study

Official Title:	Effect of Ketoconazole on the Pharmacokinetics of Intravenous (IV) Vinflunine in Patients With Advanced Cancer

Further study details as provided by Bristol-Myers Squibb:

Primary Outcome Measures:

To assess the effect of ketoconazole on the pharmacokinetics of vinflunine in patient with advanced cancer. A total of 28 blood samples will be collected [ Time Frame: Days 1 through 5 and Day 8 of Cycles 1 and 2 ]

Secondary Outcome Measures:

Evaluate the safety of vinflunine co-administered with ketoconazole and assess the safety of vinflunine in patients with advanced cancer. Safety laboratory assessments and evaluations will be collected [ Time Frame: weekly ]

Estimated Enrollment:	35
Study Start Date:	October 2005
Study Completion Date:	September 2007

Arms	Assigned Interventions
1: Experimental	Drug: vinflunine + ketaconazole vinflunine solution for injection, ketaconazole tablets, vinflunine IV, ketaconazole oral, vinflunine 80 to 320mg/m2 + ketaconazole 400 mg, vinflunine every 3 wks, ketaconazole C1 only, variable duration

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Advanced cancer excluding cancer within the blood, adequate kidney and liver function.

Exclusion Criteria:

Prior use of vinflunine, other active medical disorders, severe nerve damage

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00388557

Locations


United States, Tennessee
	Tennessee Oncology, Pllc
	Nashville, Tennessee, United States, 37203

Sponsors and Collaborators

Bristol-Myers Squibb

Investigators


Study Director:	Bristol-Myers Squibb	Bristol-Myers Squibb

More Information

BMS Clinical Trials Disclosure This link exits the ClinicalTrials.gov site

For FDA Safety Alerts and Recalls refer to the following link www.fda.gov/MEDWATCH/safety.htm This link exits the ClinicalTrials.gov site

Responsible Party:	Bristol-Myers Squibb ( Study Director )
Study ID Numbers:	CA183-009
First Received:	October 16, 2006
Last Updated:	June 27, 2008
ClinicalTrials.gov Identifier:	NCT00388557
Health Authority:	United States: Food and Drug Administration

Study placed in the following topic categories:

Clotrimazole

Miconazole

Tioconazole

Ketoconazole

Additional relevant MeSH terms:

Anti-Infective Agents

Therapeutic Uses

Antifungal Agents

Pharmacologic Actions

ClinicalTrials.gov processed this record on September 05, 2008

Sponsored by:	Bristol-Myers Squibb
Information provided by:	Bristol-Myers Squibb
ClinicalTrials.gov Identifier:	NCT00388557