TY - JOUR
T1 - Strategies for utilizing neuroimaging biomarkers in CNS drug discovery and development
T2 - CINP/JSNP working group report
AU - Suhara, Tetsuya
AU - Chaki, Shigeyuki
AU - Kimura, Haruhide
AU - Furusawa, Makoto
AU - Matsumoto, Mitsuyuki
AU - Ogura, Hiroo
AU - Negishi, Takaaki
AU - Saijo, Takeaki
AU - Higuchi, Makoto
AU - Omura, Tomohiro
AU - Watanabe, Rira
AU - Miyoshi, Sosuke
AU - Nakatani, Noriaki
AU - Yamamoto, Noboru
AU - Liou, Shyh Yuh
AU - Takado, Yuhei
AU - Maeda, Jun
AU - Okamoto, Yasumasa
AU - Okubo, Yoshiaki
AU - Yamada, Makiko
AU - Ito, Hiroshi
AU - Walton, Noah M.
AU - Yamawaki, Shigeto
N1 - Publisher Copyright:
© The Author 2016.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Despite large unmet medical needs in the field for several decades, CNS drug discovery and development has been largely unsuccessful. Biomarkers, particularly those utilizing neuroimaging, have played important roles in aiding CNS drug development, including dosing determination of investigational new drugs (INDs). A recent working group was organized jointly by CINP and Japanese Society of Neuropsychopharmacology (JSNP) to discuss the utility of biomarkers as tools to overcome issues of CNS drug development. The consensus statement from the working group aimed at creating more nuanced criteria for employing biomarkers as tools to overcome issues surrounding CNS drug development. To accomplish this, a reverse engineering approach was adopted, in which criteria for the utilization of biomarkers were created in response to current challenges in the processes of drug discovery and development for CNS disorders. Based on this analysis, we propose a new paradigm containing 5 distinct tiers to further clarify the use of biomarkers and establish new strategies for decision-making in the context of CNS drug development. Specifically, we discuss more rational ways to incorporate biomarker data to determine optimal dosing for INDs with novel mechanisms and targets, and propose additional categorization criteria to further the use of biomarkers in patient stratification and clinical efficacy prediction. Finally, we propose validation and development of new neuroimaging biomarkers through public-private partnerships to further facilitate drug discovery and development for CNS disorders.
AB - Despite large unmet medical needs in the field for several decades, CNS drug discovery and development has been largely unsuccessful. Biomarkers, particularly those utilizing neuroimaging, have played important roles in aiding CNS drug development, including dosing determination of investigational new drugs (INDs). A recent working group was organized jointly by CINP and Japanese Society of Neuropsychopharmacology (JSNP) to discuss the utility of biomarkers as tools to overcome issues of CNS drug development. The consensus statement from the working group aimed at creating more nuanced criteria for employing biomarkers as tools to overcome issues surrounding CNS drug development. To accomplish this, a reverse engineering approach was adopted, in which criteria for the utilization of biomarkers were created in response to current challenges in the processes of drug discovery and development for CNS disorders. Based on this analysis, we propose a new paradigm containing 5 distinct tiers to further clarify the use of biomarkers and establish new strategies for decision-making in the context of CNS drug development. Specifically, we discuss more rational ways to incorporate biomarker data to determine optimal dosing for INDs with novel mechanisms and targets, and propose additional categorization criteria to further the use of biomarkers in patient stratification and clinical efficacy prediction. Finally, we propose validation and development of new neuroimaging biomarkers through public-private partnerships to further facilitate drug discovery and development for CNS disorders.
KW - CNS drug development
KW - Clinical efficacy prediction
KW - Neuroimaging biomarkers
KW - Patient stratification
KW - Public-private-partnerships
UR - http://www.scopus.com/inward/record.url?scp=85019654130&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85019654130&partnerID=8YFLogxK
M3 - Review article
C2 - 28031269
AN - SCOPUS:85019654130
SN - 1461-1457
VL - 20
SP - 285
EP - 294
JO - International Journal of Neuropsychopharmacology
JF - International Journal of Neuropsychopharmacology
IS - 4
ER -