Siffledeen, Jesse
Singh, Sunny
Shulman, Scott M.
Igoe, John
Heatta-Speicher, Tobias
Leitner, Claudia
Chung, Chia Hui
Targownik, Laura
Funding for this research was provided by:
AbbVie Corporation
Article History
Received: 19 December 2023
Accepted: 23 January 2024
First Online: 16 March 2024
Declarations
:
: JS has received consultancy and/or speaking honoraria fees from AbbVie, BioJamp, Bristol Myers Squibb, Celltrion, Ferring, Fresenius Kabi, Janssen, Pfizer, and Takeda; and educational grants from AbbVie and BioJamp. SS has received speaker and consulting fees from AbbVie, Takeda, Ferring, Kabi Fresenius, BMS, Pfizer, and Janssen. SMS has received speaker fees, consultancy fees and/or Advisory board fees from AbbVie, Bristol Myers Squibb, Takeda, Gilead, BIO-Jamp, and Janssen. JI has received speaker fees, consulting fees, and advisory board fees from AbbVie, Takeda, and BioJamp, and advisory board fees from Eli Lilly. THS is an employee of AbbVie Corporation. CL is an employee of AbbVie Corporation. CHC is an employee of AbbVie Corporation. LT has received grants or contracts from AbbVie Canada, Janssen Canada, and Pfizer, Canada; received consulting fees from AbbVie, Amgen, Bristol Myers Squibb, Fresenius Kabi, Janssen, Lily, Pfizer, Sanofi, Takeda, and Viatris; has received payment or honoraria from AbbVie, Amgen, Bristol Myers Squibb, Fresenius Kabi, Janssen, Pfizer, Sanofi, Takeda, and Viatris; has participated on a Data Safety Monitoring Board or Advisory Board for Bristol Myers Squibb, GoodCap Pharmaceuticals, Janssen, Pfizer, and Takeda; and has received services from AbbVie, Bristol Myers Squibb, and Pfizer.
: Ethics Committee approval was obtained from Advarra as necessary per local laws and regulations. The study was conducted in accordance with ethical principles that have their origin in the current Declaration of Helsinki and followed the principles of International Conference Harmonization Good Clinical Practice and Good Epidemiology Practice and applicable regulatory requirements.
: All patients provided written informed consent before study inclusion.