Kato, Koji https://orcid.org/0000-0002-5815-4585
Nakamura, Sosuke
Wakana, Akira
Koh, Yasuhiro
Izutsu, Koji
Clinical trials referenced in this document:
Documents that mention this clinical trial
Pembrolizumab in Japanese patients with primary mediastinal large B-cell lymphoma: results from the KEYNOTE-A33 study
https://doi.org/10.1007/s10147-024-02627-8
Funding for this research was provided by:
Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA
MSD K.K., Tokyo, Japan
Article History
Received: 15 July 2024
Accepted: 12 September 2024
First Online: 18 September 2024
Declarations
:
: Koji Kato reports honoraria from Bristol Myers Squibb, Celgene, Dainippon-Sumitomo, Janssen, Kyowa Kirin, MSD, Mundi, and Ono; consulting or advisory roles with AbbVie, AstraZeneca, Celgene, Chugai Pharmaceutical, Daiichi Sankyo, Eisai, Janssen, and Novartis; and research funding from AbbVie, Bristol Myers Squibb, Celgene, Chugai, Daiichi Sankyo, Eisai, Janssen, Kyowa Kirin, MSD, Novartis, and Ono. Sosuke Nakamura reports employment at MSD K.K., Tokyo, Japan. Akira Wakana reports employment at MSD K.K., Tokyo, Japan, and stock ownership in Merck & Co., Inc., Rahway, NJ, USA. Yasuhiro Koh reports employment at MSD K.K., Tokyo, Japan, and stock ownership in Merck & Co., Inc., Rahway, NJ, USA. Koji Izutsu reports research grants from AstraZeneca, AbbVie, Incyte, Bristol Myers Squibb, Novartis, Janssen, Chugai, BeiGene, and Genmab. This study was designed under the responsibility of, and was supported by, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA, and MSD.K.K., Tokyo, Japan, in conjunction with the steering committee. Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA, and MSD.K.K., Tokyo, collected and analyzed the data and contributed to the interpretation of the study. All authors had full access to all of the data in the study and had final responsibility for the decision to submit for publication.
: Ethical approval of the research protocol by an Institutional Review Board: The study protocol and all amendments were approved by the appropriate institutional review boards and ethics review committees at each center. The study was conducted in accordance with the protocol, Good Clinical Practice guidelines, and the Declaration of Helsinki.
: All patients provided written informed consent before enrollment.