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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05250817
Other study ID # CA209-69K
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 9, 2021
Est. completion date January 4, 2023

Study information

Verified date June 2023
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this observational study is to determine participants' preferences for outcomes associated with first-line treatment of advanced/metastatic Non-Small Cell Lung Cancer (NSCLC) using a discrete-choice experiment (DCE).


Recruitment information / eligibility

Status Completed
Enrollment 501
Est. completion date January 4, 2023
Est. primary completion date January 4, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: The following is the inclusion criteria for pretest interviews and final online survey. Participants: - Must be 18 years of age or older - Must be a US resident. - Lung cancer participants with a physician diagnosis of NSCLC. Global Perspectives will be involved to suggest alternative strategies to a physician-confirmed diagnosis to ensure that actual cancer participants are recruited. Exclusion Criteria: - Not applicable Other protocol-defined inclusion/exclusion criteria apply

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States RTI Health Solutions Research Triangle Park North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Bristol-Myers Squibb

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Set of relative preference weights for all attribute levels included in the Discrete Choice Experiment (DCE) At Baseline
Primary Respondents' baseline understanding of attribute descriptions At Baseline
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