Lemech, Charlotte
Woodward, Natasha
Chan, Nancy
Mortimer, Joanne
Naumovski, Louie
Nuthalapati, Silpa
Tong, Bo
Jiang, Fang
Ansell, Peter
Ratajczak, Christine K.
Sachdev, Jasgit
Funding for this research was provided by:
AbbVie (n/a)
Article History
Received: 5 March 2020
Accepted: 28 May 2020
First Online: 10 June 2020
Compliance with ethical standards
:
: Charlotte Lemech.No relationships to disclose.<b>Natasha Woodward</b>Research funding (institutional) from Medivation; advisory board for Roche, Pfizer; travel, accommodations, and expenses from Roche; stock ownership in CSL; editorial writing support from Pfizer.<b>Nancy Chan</b>No relationships to disclose.<b>Joanne Mortimer</b>Consulting or advisory role for Novartis, Pfizer, Puma Biotechnology; honoraria from Novartis.<b>Louie Naumovski, Silpa Nuthalapati, Bo Tong, Fang Jiang, Peter Ansell, and Christine K. Ratajczak</b>AbbVie employees and may own stock.<b>Jasgit Sachdev</b>Research funding from Pfizer, Celgene, Genentech; consulting or advisory role for Celgene, Puma Biotechnology, TTC Oncology, Pfizer, Novartis, TapImmune, Ipsen, Tempus; travel accommodations, and expenses from Celgene; honoraria from Celgene, Ipsen, Puma Biotechnology, Novartis, Pfizer, Tempus.AbbVie is committed to responsible data sharing regarding the clinical trials we sponsor. This includes access to anonymized, individual and trial-level data (analysis data sets), as well as other information (e.g., protocols and clinical study reports), as long as the trials are not part of an ongoing or planned regulatory submission. This includes requests for clinical trial data for unlicensed products and indications.These clinical trial data can be requested by any qualified researchers who engage in rigorous, independent scientific research, and will be provided following review and approval of a research proposal and statistical analysis plan (SAP) and execution of a data sharing agreement (DSA). Data requests can be submitted at any time and the data will be accessible for 12 months, with possible extensions considered. For more information on the process, or to submit a request, visit the following link: ExternalRef removed.
: All patients provided their informed consent. All study procedures were conducted in accordance with the ethical standards of the 1964 Declaration of Helsinki and Good Clinical Practice guidelines. The protocol received institutional review board approval.
: Informed consent was obtained from all individual participants included in the study.