YERVOY® Risk Minimization Tool Effectiveness Evaluation Survey
NCT ID: NCT02224768
Last Updated: 2015-12-21
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
158 participants
OBSERVATIONAL
2015-07-31
2015-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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HCP and Patient inclusion
HCP inclusion - HCP Experience with treatment of patients with study compound who have been exposed to risk minimization tools
Patient inclusion - Patients treated with study compound as per label who have been exposed to the risk minimization materials
Ipilimumab
Interventions
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Ipilimumab
Eligibility Criteria
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Inclusion 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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Bristol-Myers Squibb
Princeton, New Jersey, United States
Local Institution
St Ives, Cambridgeshire, United Kingdom
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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CA184-242
Identifier Type: -
Identifier Source: org_study_id