Brookes, Ella https://orcid.org/0009-0001-9710-3799
Coşkun, Ufuk
O’Donnell, Christina
Zikos, Efstathios
Martincova, Renata
Chao, Jingdong
Giruparajah, Mohana
Romero, Beverly
Funding for this research was provided by:
Sanofi
Regeneron Pharmaceuticals
Article History
Accepted: 23 June 2025
First Online: 22 July 2025
Declarations
:
: This study was sponsored by Sanofi and Regeneron Pharmaceuticals, Inc.
: Ufuk Coşkun and Christina O’Donnell are employees of ICON Clinical Research who were contracted to conduct the interviews and may hold stock or stock options in the company. Beverly Romero and Mohana Giruparajah were employed at ICON Clinical Research during the study; currently are employed by Sprout Health Solutions. Ella Brookes and Renata Martincova are employees of Sanofi and may hold stock or stock options in the company. Jingdong Chao is an employee of Regeneron Pharmaceuticals Inc. and may hold stock or stock options in the company. Efstathios Zikos is an external contractor working for Sanofi via Barrington James.
: This study was conducted in accordance with the principles outlined in the Declaration of Helsinki. Ethics approval was obtained from a central institutional review board (Advarra, Inc. for USA and Canada), as well as by regional and local boards (Argentina: Comité de Ética de Protocols de Investigación del Hospital Italiano de Buenos Aires: Comité de Ética en Investigación and Center for the Study of Infectious Diseases SA [Stamboulian Health Services] Clinical Research Ethics Committee; Canada: Health Ethics Research Board of Alberta Community Health Committee; Germany: Landesärztekammer Rheinland-Pfalz Ethik-Kommission and Technische Universität Dresden: Ethikkommission an der TU Dresden).
: This study adheres to the ICMJE Recommendations for patient privacy and follows ethical guidelines to ensure the protection of patient information. All participants in this study provided written informed consent as part of institutional review board-approved consent forms. The consent forms included information about the study’s purpose, the use of aggregated results in reports and publications, and the participants’ right to withdraw from the study at any time without penalty. Identifying information has been removed to ensure anonymity, and no individual identifiers are included in any reports or publications resulting from this study. The consent forms are securely filed. We have taken all necessary steps to ensure that identifying details are omitted from the article. Patient data have not been altered or falsified to achieve anonymity. The journal editorial office will not collect or archive consent forms but retains the right to request verification of their existence if needed.
: Not applicable.
: This study involved qualitative interviews, and because of the confidential nature of the data, the complete transcripts cannot be shared publicly. Researchers interested in accessing the data for verification or further analysis may contact the corresponding author to discuss potential access under strict confidentiality agreements.
: Not applicable.
: Concept and design: EB, RM, BR, JC. Acquisition of data: UC, MG, BR. Analysis and interpretation of data: UC, CO, BR, EB, EZ, JC. Drafting of the article: CO, UC, MG. Critical revision of the article for important intellectual content: EB, UC, CO, EZ, RM, JC, MG, BR.