YERVOY® Risk Minimization Tool Effectiveness Evaluation Survey

NCT ID: NCT02224768

Last Updated: 2015-12-21

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

158 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-07-31

Study Completion Date

2015-11-30

Brief Summary

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To evaluate the effectiveness of the YERVOY® educational Risk Minimization (RM) tools in terms of awareness about these tools, their utilization, knowledge and comprehension of Immune Related Adverse Reaction (irAR)s, and appropriate behavior by Healthcare Professional (HCP)s and patients

Detailed Description

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A total sample size of 160 to 200 HCPs and 160 to 200 patients

Conditions

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Advanced Melanoma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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

Intervention Type DRUG

Interventions

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Ipilimumab

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* HCP experienced in the treatment of patients with the research compound and patients that have received at least one dose
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bristol-Myers Squibb

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Local Institution

St Ives, Cambridgeshire, United Kingdom

Site Status

Countries

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United States United Kingdom

Related Links

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Other Identifiers

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CA184-242

Identifier Type: -

Identifier Source: org_study_id