Howell, Timothy A.
Matza, Louis S. http://orcid.org/0000-0001-6374-5948
Jun, Monika P.
Garcia, Jacob
Powers, Annette
Maloney, David G.
Funding for this research was provided by:
Bristol-Myers Squibb
Article History
Accepted: 30 November 2021
First Online: 7 February 2022
Declarations
:
: Not applicable.
: Not applicable.
: This study was funded by Juno Therapeutics, a Bristol Myers Squibb Company.
: This study was funded by Juno Therapeutics, a Bristol Myers Squibb Company.
: Timothy A. Howell and Louis S. Matza are employees of Evidera, which received funding from Bristol Myers Squibb to conduct the analyses. Monika P. Jun and Annette Powers are employees of Bristol Myers Squibb and hold stock in Bristol Myers Squibb. Jacob Garcia was an employee of Bristol Myers Squibb when the work reported in this manuscript was conducted and holds stock in Bristol Myers Squibb. His current affiliation is Umoja Biopharma, Seattle, WA, USA. David G. Maloney has received consultancy fees and honoraria from A2 Biotherapeutics, Amgen, BioLineRx, Celgene (a Bristol Myers Squibb Company), Genentech, Gilead Sciences, Juno Therapeutics (a Bristol Myers Squibb Company), Kite Pharma (a Gilead Company), MorphoSys, Novartis, and Pharmacyclics, and grants for research from Celgene (a Bristol Myers Squibb Company), Juno Therapeutics (a Bristol Myers Squibb Company), and Kite Pharma (a Gilead Company).
: Bristol Myers Squibb policy on data sharing may be found at https://www.bms.com/researchers-and-partners/independent-research/data-sharing-request-process.html.
: Not applicable.
: Timothy A. Howell and Louis S. Matza co-directed the study, including study design, health state development, data analysis, and data interpretation, and drafted the manuscript. Monika P. Jun and Annette Powers assisted with the study design, health state content, and data interpretation. Jacob Garcia and David G. Maloney provided clinical input to help shape the study design, health states, and interpretation. All authors provided input and approval.
: The study was approved by the appropriate institutional and national research ethics committee (Ethical and Independent Review Services, Study 19018) and was performed in accordance with the ethical standards as laid down in the 1964 Declaration of Helsinki and its later amendments.
: Participants provided written informed consent before completing study procedures, and all procedures and materials were approved by an independent institutional review board (Ethical and Independent Review Services, Study 19018).