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Completed Phase 2 Interventional Results available

Dasatinib (BMS-354825) in Subjects With Myeloid Blast Phase Chronic Myeloid Leukemia Resistant to or Intolerant of Imatinib Mesylate

ClinicalTrials.gov ID: NCT00101816

Public ClinicalTrials.gov record NCT00101816. 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 Sep 2, 2026, 4:10 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

A Phase II Study of BMS-354825 in Subjects With Myeloid Blast Phase Chronic Myeloid Leukemia Resistant to or Intolerant of Imatinib Mesylate

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to see what effect an investigational drug (BMS-354825) has on subjects who are currently in the myeloid blast phase of chronic myeloid leukemia (CML) and who are either resistant to or intolerant of imatinib mesylate. Another purpose of the study is to see what side effects this drug may have on subjects.

Study identification

NCT ID
NCT00101816
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
124 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Nov 30, 2004
Primary completion
Jul 31, 2006
Completion
Feb 29, 2008
Last update posted
Aug 9, 2010

2004 – 2008

United States locations

U.S. sites
23
U.S. states
18
U.S. cities
23
Facility City State ZIP Site status
Local Institution Birmingham Alabama
Local Institution Anaheim California
Local Institution Los Angeles California
Local Institution Stanford California
Local Institution Vallejo California
Local Institution Denver Colorado
Local Institution Jacksonville Florida
Local Institution Tampa Florida
Local Institution Atlanta Georgia
Local Institution Chicago Illinois
Local Institution Kansas City Kansas
Local Institution Baltimore Maryland
Local Institution Boston Massachusetts
Local Institution Detroit Michigan
Local Institution St Louis Missouri
Local Institution Hackensack New Jersey
Local Institution New Brunswick New Jersey
Local Institution New York New York
Local Institution Portland Oregon
Local Institution Pittsburgh Pennsylvania
Local Institution Nashville Tennessee
Local Institution Houston Texas
Local Institution Seattle Washington

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 39 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00101816, 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 Aug 9, 2010 · Synced Sep 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00101816 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →