• Joshua D Vardigan, Parul S Pall, Dillon S McDevitt, ChienJung Huang, Michelle K Clements, Yuxing Li, Richard L Kraus, Michael J Breslin, Christopher J Bungard, Mikhail I Nemenov, Mikhail Klukinov, Chritopher S Burgey, Mark E Layton, Shawn J Stachel, Henry S Lange, Alan T Savitz, Vincent P Santarelli, Darrell A Henze, and Jason M Uslaner.
• Merck Sharp & Dohme LLC, a subsidiary of Merck & Co Inc, Rahway, NJ, United States.
• Pain. 2024 Oct 8.

AbstractVoltage-gated sodium (Nav) channels present untapped therapeutic value for better and safer pain medications. The Nav1.8 channel isoform is of particular interest because of its location on peripheral pain fibers and demonstrated role in rodent preclinical pain and neurophysiological assays. To-date, no inhibitors of this channel have been approved as drugs for treating painful conditions in human, possibly because of challenges in developing a sufficiently selective drug-like molecule with necessary potency not only in human but also across preclinical species critical to the preclinical development path of drug discovery. In addition, the relevance of rodent pain assays to the human condition is under increasing scrutiny as a number of mechanisms (or at the very least molecules) that are active in rodents have not translated to humans, and direct impact on pain fibers has not been confirmed in vivo. In this report, we have leveraged numerous physiological end points in nonhuman primates to evaluate the analgesic and pharmacodynamic activity of a novel, potent, and selective Nav1.8 inhibitor compound, MSD199. These pharmacodynamic biomarkers provide important confirmation of the in vivo impact of Nav1.8 inhibition on peripheral pain fibers in primates and have high translational potential to the clinical setting. These findings may thus greatly improve success of translational drug discovery efforts toward better and safer pain medications, as well as the understanding of primate biology of Nav1.8 inhibition broadly.Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain.

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