Langslet, Gisle
Hovingh, G. Kees
Guyton, John R.
Baccara-Dinet, Marie T.
Letierce, Alexia
Manvelian, Garen
Farnier, Michel
Funding for this research was provided by:
Sanofi (n/a)
Regeneron Pharmaceuticals (n/a)
Article History
First Online: 4 May 2020
Compliance with Ethical Standards
:
: Dr. Langslet has received speaker and expert witness fees from Sanofi, Amgen, and Boehringer Ingelheim. Professor Hovingh is a holder of a Vidi grant (016.156.445) from the Netherlands Organisation for Scientific Research (NWO) and from Klinkerpad; has received research support from Aegerion, Amgen, and Sanofi; has served as a consultant and received speaker fees from Amgen; Aegerion; Sanofi; Regeneron Pharmaceuticals, Inc.; and Pfizer; and has been employed part-time by Novo Nordisk AS, Copenhagen, Denmark, since April 2019. Professor Guyton has received research support from Sanofi, Regeneron Pharmaceuticals, Inc., Amgen, and Amarin; and has served as a consultant for Amgen, and FH Foundation. Drs. Baccara-Dinet and Letierce are stockholders and employees of Sanofi. Dr. Manvelian is a stockholder and an employee of Regeneron Pharmaceuticals, Inc. Dr. Farnier has received research support from Sanofi/Regeneron Pharmaceuticals, Inc.; Amgen; and Merck and Co; has served as a consultant for Sanofi/Regeneron Pharmaceuticals, Inc.; Pfizer; Amgen; Merck and Co; Eli Lilly; AstraZeneca; Kowa; Akcea/Ionis; Amarin; and Servier; and has received speaker fees from Sanofi/Regeneron Pharmaceuticals, Inc.; Abbott; Amgen; Merck and Co; Pfizer; and Mylan.
: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
: Informed consent was obtained from all individual participants included in the study.