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Active, Not Recruiting

Studying First Line Treatment of Chronic Myeloid Leukemia (CML) in a Real-world Setting - CA180-330

Updated: 19 January, 2018   |   ClinicalTrials.gov

Print Friendly Summary

CONSIDERING THIS TRIAL?
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Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.

Trial Details

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
First line TKI treatment: Dasatinib
Other: Non-Interventional
First line TKI treatment: Imatinib
Other: Non-Interventional
First line TKI treatment: Nilotinib
Other: Non-Interventional
Imatinib treated patients
Other: Non-Interventional

Key Eligibility Criteria

For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com. Inclusion Criteria: - Newly-diagnosed chronic phase chronic myeloid leukemia (CP-CML) patients who started their first-line Tyrosine Kinase Inhibitor (TKI) treatment on imatinib, dasatinib or nilotinib in accordance with the timelines below - 18 years or older at time of of CP-CML diagnosis a) Imatinib Cohorts - Patients who started their first-line Imatinib treatment between January 2, 2008 and September 30, 2010.Patients fitting this criterion are defined as retrospective Imatinib patients − Patients who started their first-line Imatinib treatment on or after October 1, 2010 b) Dasatinib Cohort - Patients who started their first-line Dasatinib treatment after the drug was approved in this indication c) Nilotinib Cohort - Patients who started their first-line Nilotinib treatment after the drug was approved in this indication - Patients are also eligible when they have already switched to a subsequent therapy (TKI or other) at the time of enrollment, as long as their first-line and subsequent CML treatment information is available at site for data entry into the study Electronic Case Report Form (eCRF) - Receiving treatment at medical practice (eg. community-based, office-based, hospital-based, academic setting, oncology center) Exclusion Criteria: - Patients who are participating in an interventional trial which may influence the management of their CML disease will be excluded Discontinuation Criteria: - Enrolled patients who join an interventional trial which may influence the management of their CML disease will be excluded at the time of entry into the interventional trial

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Have questions? Live support is available 24/7 - Call 855-907-3286 or email clinical.trials@bms.com

Have questions? Live support is available 24/7 -
Call 855-907-3286 or email clinical.trials@bms.com