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YERVOY® Risk Minimization Tool Effectiveness Evaluation Survey

YERVOY Risk Minimisation Tool Evaluation Survey

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02224768
Enrollment
158
Registered
2014-08-25
Start date
2015-07-31
Completion date
2015-11-30
Last updated
2015-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced Melanoma

Brief summary

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

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

Interventions

DRUGIpilimumab

Sponsors

Bristol-Myers Squibb
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: * HCP experienced in the treatment of patients with the research compound and patients that have received at least one dose

Design outcomes

Primary

MeasureTime frameDescription
The proportion of YERVOY HCPs that are aware of the existence of the risk communications tools and how the tools were accessed (i.e. paper or electronic versions)6 monthsDistribution metrics and awareness of the tools from responses through the survey will be analysed and descriptive statistics will be used within the different participant groups
Questionnaire: Who uses the RM communication tools, how, when they are used and how often they are used6 monthsWeb downloads metrics will be collected and the usage of tools from responses in the survey will be analysed, and descriptive statistics will be used within the participant groups
Level of knowledge and comprehension of the key elements of important identified risks associated with YERVOY treatment based on the scores obtained from the Questionnaire Surveys6 monthsKnowledge and comprehension in HCPs and patients, the knowledge surveys will provide the following data 1. Total number of responses to the question including the proportions of correct answers to questions where appropriate 2. Number or frequency and proportion of response options selected 3. Percentage of responses/total responses per option 4. Mean value and standard deviation (for appropriate questions) From the obtained data, Acceptable levels of correct responses will be determined, post data analysis, reporting and discussion with EMA, to set baseline levels for potential future evaluations and then the scores will be assessed
HCP and patient behaviours via behavioural questions and scenarios based on the scores obtained from the Questionnaire Surveys6 monthsFor determining appropriate behaviours in HCPs and patients, ideal expected behaviours will be mapped to the ideal care pathway from the Failure Modes and Effects Analysis (FMEA) as described in the RMP. The metrics will show: 1. Total of number of participants answering the question. 2. Proportions of participants providing correct answers (to identify knowledge and comprehension) 3. Proportion of participants showing expected (ideal) behaviour - i.e. correct answers to individual questions. 4. Proportion of participants showing non-ideal behaviour - i.e. partially correct or incorrect answers to individual questions. Analysis will examine knowledge, comprehension and behaviours for different participant types (HCP, Hospital type and Country)

Countries

United Kingdom, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026