Healthcare Costs Among Patients With CML Receiving Dasatinib or Nilotinib in a Commercial and Medicare Population
NCT ID: NCT02363868
Last Updated: 2015-07-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
186 participants
OBSERVATIONAL
2014-02-28
2014-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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CML subjects receiving Dasatinib
CML receiving dasatinib as first or second line therapy will be conducted to assess healthcare costs
No interventions assigned to this group
CML subjects receiving Nilotinib
CML receiving nilotinib as first or second line therapy will be conducted to assess healthcare costs
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9 CM) code for CML (205.1x)
* At least 2 prescriptions for dasatinib or nilotinib from July 1, 2008 to June 31, 2013
* Continuous eligibility for the 6 months pre- and post-index date (defined as the date of first fill for dasatinib or nilotinib)
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Bristol-Myers Squibb
INDUSTRY
Responsible Party
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Principal Investigators
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Bristol-Myers Squibb
Role: STUDY_DIRECTOR
Bristol-Myers Squibb
Locations
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Franklin Pharmaceutical Consulting, Llc
Clinton, South Carolina, United States
Countries
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Related Links
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BMS clinical trial educational resource
Investigator Inquiry form
Other Identifiers
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CA180-568
Identifier Type: -
Identifier Source: org_study_id
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