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Completed Phase 2 Interventional Results available

Study of Dasatinib (BMS-354825) in Patients With Accelerated Phase Chronic Myeloid Leukemia

ClinicalTrials.gov ID: NCT00101647

Public ClinicalTrials.gov record NCT00101647. 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 Oct 22, 2026, 12:08 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 Accelerated 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 clinical research study is to learn if BMS-354825 will have activity, defined by hematologic response, in subjects who have accelerated phase chronic myeloid leukemia (CML) who are resistant to or intolerant to imatinib mesylate. The safety of this treatment will also be studied.

Study identification

NCT ID
NCT00101647
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
197 participants

Conditions and interventions

Interventions

Drug

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
Dec 2004 (Type not available)
Primary completion
Aug 2006 (Actual)
Completion
Mar 2008 (Actual)
Last update posted
Apr 15, 2011

2004 – 2008

United States locations

U.S. sites
21
U.S. states
16
U.S. cities
21
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 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 York New York — —
Local Institution Portland Oregon — —
Local Institution Pittsburgh Pennsylvania — —
Local Institution Nashville Tennessee — —
Local Institution Dallas Texas — —
Local Institution Houston Texas — —

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 49 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00101647, 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 15, 2011 · Synced Oct 22, 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 public registry record, listed eligibility criteria, and available contact information for NCT00101647 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →