Ni, Shumao
Ma, Sheng
Yu, Yingying
Yu, Zhenwen
Zhu, Yujia
Sun, Xiaofen
Li, Lin
Sun, Caixia
Wang, Hui
Peng, Peng
Gu, Zheming
Zhang, Hua
Wu, Frank
Miao, Liyan
Fan, Jean http://orcid.org/0009-0002-0135-6968
Funding for this research was provided by:
TransThera Sciences (Nanjing), Inc.
Article History
Accepted: 19 August 2024
First Online: 5 September 2024
Declarations
:
: This work was funded by TransThera Sciences (Nanjing), Inc.
: Jean Fan is an employee of Trans Thera Sciences (US), Inc., which is a wholly owned subsidiary of TransThera Sciences (Nanjing), Inc. Shumao Ni, Yingying Yu, Yujia Zhu, Xiaofen Sun, Lin Li, Caixia Sun, Hui Wang, Peng Peng, and Frank Wu are all employees of TransThera Sciences (Nanjing), Inc. Shumao Ni, Sheng Ma, Yingying Yu, Zhenwen Yu, Yujia Zhu, Xiaofen Sun, Lin Li, Caixia Sun, Hui Wang, Peng Peng, Zheming Gu, Hua Zhang, Frank Wu, Liyan Miao, and Jean Fan have no conflicts of interest that are directly relevant to the content of this article.
: All data used and/or analyzed during this study are available from the corresponding author on reasonable request.
: The study was conducted in compliance with the Helsinki Declaration and the International Council for Harmonization Good Clinical Practice guidelines and approved by the Hospital Ethics (Ethics approval number: 2021230, 12 October 2021).
: All subjects provided written informed consent prior to study initiation.
: Not applicable.
: Not applicable.
: Shumao Ni and Sheng Ma contributed equally to this work. S.M.N. and J.F. were responsible for data analysis, interpretation of the data, drafting the manuscript, and final approval of the version to be published and were accountable for all aspects of the work in ensuring that questions or comments raised by the reviewers have been addressed and incorporated, and questions related to the accuracy or integrity are appropriately investigated and resolved. S.M.N., S.M., Y.Y.Y., Y.J.Z., C.X.S., P.P., H.Z., F.W., and L.Y.M. participated in study design. S.M., H.Z., and L.Y.M. participated in clinical trials for data acquisition. Z.W.Y. and Z.M.G. participated in data analysis. X.F.S. participated in the preparation of capsules. L.L. synthesized the reference substances. S.M.N., Y.Y.Y., and H.W. participated in project administration. P.P. and F.W. provided financial support. All authors reviewed the manuscript.