Harrold, Leslie R. http://orcid.org/0000-0002-0170-2747
Zueger, Patrick
Nowell, W. Benjamin
Blachley, Taylor
Schrader, Amy
Lakin, Paul R.
Curtis, David
Stradford, Laura
Venkatachalam, Shilpa
Tundia, Namita
Patel, Pankaj A.
Funding for this research was provided by:
CorEvitas LLC
AbbVie
Article History
Received: 21 June 2023
Accepted: 18 August 2023
First Online: 20 September 2023
Declarations
:
: Financial arrangements of the authors with companies whose products may be related to the present manuscript are listed, as declared by the authors. Leslie R. Harrold: Employee and shareholder of CorEvitas, consultant to AbbVie, Bristol Myers Squibb, and Roche, speaker’s bureau for Bristol Myers Squibb. Patrick Zueger: Employee of AbbVie and may hold stock or stock options. W. Benjamin Nowell: Employee of Global Healthy Living Foundation, an independent nonprofit research organization, principal investigator for studies with grant support from AbbVie, Amgen, Janssen, and Scipher Medicine. Taylor Blachley: Former employee of CorEvitas; current employee of Syneos Health. Amy Schrader: Employee of CorEvitas. Paul R. Lakin: Employee of CorEvitas. David Curtis: Employee of Global Healthy Living Foundation, an independent nonprofit research organization. Laura Stradford: Employee of Global Healthy Living Foundation, an independent nonprofit research organization. Shilpa Venkatachalam: Employee of Global Healthy Living Foundation, an independent nonprofit research organization. Namita Tundia: Former employee of AbbVie and may hold stock or stock options; current employee of EMD Serono. Pankaj A. Patel: Employee of AbbVie and may hold stock or stock options.
: The CorEvitas RA Registry is conducted in accordance with the Declaration of Helsinki 1964 and its later amendments. All participating investigators were required to obtain full board approval for conducting research involving human subjects. Sponsor-level and site-level approval for this sub-study was obtained from the New England Independent Review Board (NEIRB; no. 20201379). All patients provided written informed consent and authorization prior to participating in the study.