Understanding Exposure-Receptor Occupancy Relationships for Metabotropic Glutamate Receptor 5 Negative Allosteric Modulators across a Range of Preclinical and Clinical Studies
The metabotropic glutamate receptor 5 (mGlu(5)) is a recognized central nervous system therapeutic target for which several negative allosteric modulator (NAM) drug candidates have or are continuing to be investigated for various disease indications in clinical development. Direct measurement of tar...
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Veröffentlicht in: | The Journal of pharmacology and experimental therapeutics 2021-04, Vol.377 (1), p.157-168 |
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Sprache: | eng |
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Zusammenfassung: | The metabotropic glutamate receptor 5 (mGlu(5)) is a recognized central nervous system therapeutic target for which several negative allosteric modulator (NAM) drug candidates have or are continuing to be investigated for various disease indications in clinical development. Direct measurement of target receptor occupancy (RO) is extremely useful to help design and interpret efficacy and safety in nonclinical and clinical studies. In the mGlu(5) field, this has been successfully achieved by monitoring displacement of radiolabeled ligands, specifically binding to the mGlu(5) receptor, in the presence of an mGlu(5) NAM using in vivo and ex vivo binding in rodents and positron emission tomography imaging in cynomolgus monkeys and humans. The aim of this study was to measure the RO of the mGlu(5) NAM HTL0014242 in rodents and cynomolgus monkeys and to compare its plasma and brain exposure-RO relationships with those of clinically tested mGlu(5) NAMs dipraglurant, mavoglurant, and basimglurant. Potential sources of variability that may contribute to these relationships were explored. Distinct plasma exposure-response relationships were found for each mGlu(5) NAM, with >100-fold difference in plasma exposure for a given level of RO. However, a unified exposure-response relationship was observed when both unbound brain concentration and mGlu(5) affinity were considered. This relationship showed |
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ISSN: | 0022-3565 1521-0103 |
DOI: | 10.1124/jpet.120.000371 |