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Drug Discovery Efforts for Pain Indications: Ion
Channels and GPCRs
Sponsored by
APS Translation
Physiology Group
and the Liaison with Industry Committee
Translational Physiology Track
Tuesday, May 1 — 8:00-10:00 AM
Washington, DC Convention Center — Room 146C
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| Chaired: |
Michael Finley, Johnson & Johnson
Pharmaceutical R&D
William Martin, Theravance |
Although acute pain sensation of noxious
stimuli is critical to survival, chronic activation of the pain
pathway(s) through nerve damage and/or inflammatory responses can become
debilitating. Many current pain medications carry side-effects that
limit their use (e.g. addiction for opioids and heart arrhythmias for
COX-2 inhibitors). In addition, there still remains significant unmet
medical need for effective pain treatments, particularly in the area of
neuropathic pain. Current drug discovery efforts to treat chronic pain
problems have focused on new molecular targets that address the
underlying mechanisms of pain sensation. This symposium brings together
several experts from industry and academia focusing on novel ion channel
or GPCR targets for treating chronic pain. Each speaker will discuss the
mechanistic rational for the target and describe the drug screening and
testing strategies employed to identify novel therapeutics.
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8:00 AM |
Therapeutic
opportunities in endocannabinoid transport inhibition.
Chris Felder,
Eli Lilly and Company
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8:30 AM |
Peripheral nerve sodium channel blockers as
analgesics: efficacy and functional selectivity.
Birgit Priest, Merck and Company
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9:00 AM |
TRPM8: a novel pain target comes in from the
cold.
Christopher Flores, Johnson & Johnson Pharmaceutical R&D
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9:30 AM |
Sensing the pain of a heart attack.
Ed McCleskey, Oregon Hlth. Sci. Univ.
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