Document is current

Article History

Received: 3 June 2022

Accepted: 31 August 2022

First Online: 1 December 2022

Declarations

:

: The study protocol was approved by the Ministry of Food and Drug Safety and Institutional Review Board (IRB) of participating institution approved and that the guidelines outlined in the Declaration of Helsinki were followed. Written informed consent was obtained from all patients. Participating IRB were as following.IRB of Samsung Medical Center, IRB of Bundang CHA Hospital, IRB of Seoul Medical Center, IRB of Ajou University Hospital, IRB of Dong-A University Hospital, IRB of Dongguk University Ilsan Hospital, IRB of Gachon University Gil Medical Center, IRB of Hanyang University Hospital, IRB of Seoul National University Bundang Hospital, IRB of Chungnam National University Hospital, IRB of Kangbuk Samsung Hospital, IRB of Yonsei University College of Medicine, IRB of Dongsan Medical Center, IRB of Ewha Womans University Hospital, IRB of Dankuk Unversity Hospital, IRB of Seoul National University Hospital.

: The written informed consent for the publication was obtained from all patients. These details were included in informed consent form.

: This study was initiated and financially supported by Boryung Corporation, Seoul, Republic of Korea (Project No: BR-FARC-CT-301). The sponsor supplied the study drug, laboratory tests and data analysis. The funding body did not play a role in data interpretation. Su-Eun Han is employees of Boryung Corporation.