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Authors
Becker, Brandon
Bracher, Marguerite http://orcid.org/0000-0001-9423-6097
Chauhan, Deven
Rendas-Baum, Regina
Lin, Xiaochen
Raymond, Kimberly
O’Connor, Meaghan
Kosinski, Mark
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Funding
Funding for this research was provided by:
GSK
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Article History
Received: 14 May 2021
Accepted: 17 November 2021
First Online: 11 December 2021
Declarations
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: For study HO-16-16897, full Institutional Review Board (IRB) approval was obtained from RCRC IRB (USA) prior to recruitment and written informed consent was obtained prior to patient interviews; all interview guides, including revisions, were approved by the IRB prior to their use. Patients were compensated for their time and involvement in the study with a $100 payment card, sent by post following the interview. For study 206577, Copernicus IRB (USA) provided ethical approval of the study and written informed consent was obtained prior to collecting patient data and interviews. Patients were compensated for their time and involvement in the study with $125 on completion of the interview. Study 206981 was overseen by the New England IRB (USA), who also approved the informed consent form and interview guides; written informed consent was obtained prior to data collection. Patients were compensated for their time and involvement in the study with a $150 Visa gift card.
: Not applicable.
: MB and DC are employees and stockholders of GSK. BB is a former employee of GSK and is an employee and stockholder of Bristol-Myers Squibb. XL, KR, RR-B, MO’C and MK are employees of QualityMetric Incorporated, LLC.
