Jones, Robin L.
Mo, Gary
Baldwin, John R.
Peterson, Patrick M.
Ilaria, Robert L. Jr.
Conti, Ilaria
Cronier, Damien M.
Tap, William D.
Funding for this research was provided by:
Eli Lilly and Company
Article History
Received: 27 September 2018
Accepted: 1 November 2018
First Online: 8 November 2018
<!--Emphasis Type='Bold' removed-->Compliance with ethical standards
:
: RLJ reports consulting work with Blueprint, Deciphera, Immune Design, Merck, Clinigen, Pharmamar, and Eisai. GM, RLI, IC, and DMC report a patent pending for dosing regimen assigned to ImClone LLC, a wholly owned subsidiary of Eli Lilly and Company. WDT reports a patent pending for Companion Diagnostic for CDK4 inhibitors − 14/854,329 for the identification and development of biomarkers for CDK4 inhibition in cancer. WDT reports Advisory Board, consulting, and travel expense reimbursement for Eli Lilly and Company, EMD Serono, Novartis, Eisai, Janssen, Immune Design, Adaptimmune, Daiichi Sankyo, Blueprint, and Loxo for the purposes of discussing cancer drug development, all outside the submitted work. WDT also reports serving as IDMC chair for sarcoma clinical trial with Morphotek, outside the submitted work. GM and PMP are full-time employees of Eli Lilly and Company; RLI, IC, DMC, and JRB are former employees of Eli Lilly and Company; GM, PMP, RLI, IC, and DMC are current shareholders of Eli Lilly and Company.
: 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 the individual participants included in the study.