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Completed No phase listed Observational Accepts healthy volunteers

A Study of Dasatinib to See How Liver Impaired and Healthy Subjects Process and React to the Study Drug

ClinicalTrials.gov ID: NCT00382668

Public ClinicalTrials.gov record NCT00382668. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 3, 2026, 7:25 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Single-Dose Pharmacokinetics of Dasatinib in Subjects With Hepatic Impairment Compared to Healthy Adult Subjects

Study identification

NCT ID
NCT00382668
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
40 participants

Conditions and interventions

Conditions

Interventions

  • Dasatinib Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2006
Primary completion
Jul 31, 2007
Completion
Jul 31, 2007
Last update posted
Apr 13, 2011

2006 – 2007

United States locations

U.S. sites
4
U.S. states
2
U.S. cities
4
Facility City State ZIP Site status
University Of Miami Miami Florida 33136
Comprehensive Phase One Miramar Florida 33025
Orlando Clinical Research Center Orlando Florida 32809
New Orleans Center For Clinical Research Knoxville Tennessee 37920

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00382668, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 13, 2011 · Synced May 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00382668 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →