TY - JOUR
T1 - Molecular Imaging in Drug Discovery and Development
AU - Lindner, Jonathan R.
AU - Link, Jeanne
N1 - Funding Information:
Dr Lindner has investigator-initiated grants from GE Healthcare and Pfizer, Inc. The other author reports no conflicts.
Funding Information:
Dr Lindner is supported by grants R01-HL078610 and R01-HL130046 from the National Institutes of Health, Bethesda, MD. Dr Lindner is also supported by grant 14-14NSBRI1-0025 from the National Space Biomedical Research Institute. Dr Link is supported by the National Cancer Institute grant P01CA042045.
Publisher Copyright:
© 2018 American Heart Association, Inc.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Noninvasive imaging has played an increasing role in the process of cardiovascular drug development. This review focuses specifically on the use of molecular imaging, which has been increasingly applied to improve and accelerate certain preclinical steps in drug development, including the identification of appropriate therapeutic targets, evaluation of on-target and off-target effects of candidate therapies, assessment of dose response, and the evaluation of drug or biological biodistribution and pharmacodynamics. Unlike the case in cancer medicine, in cardiovascular medicine, molecular imaging has not been used as a primary surrogate clinical end point for drug approval. However, molecular imaging has been applied in early clinical trials, particularly in phase 0 studies, to demonstrate proof-of-concept or to explain variation in treatment effect. Many of these applications where molecular imaging has been used in drug development have involved the retasking of technologies that were originally intended as clinical diagnostics. With greater experience and recognition of the rich information provided by in vivo molecular imaging, it is anticipated that it will increasingly be used to address the enormous time and costs associated with bringing a new drug to clinical launch.
AB - Noninvasive imaging has played an increasing role in the process of cardiovascular drug development. This review focuses specifically on the use of molecular imaging, which has been increasingly applied to improve and accelerate certain preclinical steps in drug development, including the identification of appropriate therapeutic targets, evaluation of on-target and off-target effects of candidate therapies, assessment of dose response, and the evaluation of drug or biological biodistribution and pharmacodynamics. Unlike the case in cancer medicine, in cardiovascular medicine, molecular imaging has not been used as a primary surrogate clinical end point for drug approval. However, molecular imaging has been applied in early clinical trials, particularly in phase 0 studies, to demonstrate proof-of-concept or to explain variation in treatment effect. Many of these applications where molecular imaging has been used in drug development have involved the retasking of technologies that were originally intended as clinical diagnostics. With greater experience and recognition of the rich information provided by in vivo molecular imaging, it is anticipated that it will increasingly be used to address the enormous time and costs associated with bringing a new drug to clinical launch.
KW - cardiovascular agents
KW - drug approval
KW - drug discovery
KW - molecular imaging
KW - molecular medicine
UR - http://www.scopus.com/inward/record.url?scp=85048377715&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85048377715&partnerID=8YFLogxK
U2 - 10.1161/CIRCIMAGING.117.005355
DO - 10.1161/CIRCIMAGING.117.005355
M3 - Article
C2 - 29449411
AN - SCOPUS:85048377715
SN - 1941-9651
VL - 11
JO - Circulation. Cardiovascular imaging
JF - Circulation. Cardiovascular imaging
IS - 2
M1 - e005355
ER -