mportant milestone for us," said Neil Kurtz, M.D., President and Chief
Executive Officer of TorreyPines. "We believe tezampanel has the potential
to offer migraine patients an important new treatment option with a novel
mechanism of action and we remain on track to announce top line results
from the study during the fourth quarter of this year."
In previous clinical trials, tezampanel has been administered to more
than 200 healthy adult volunteers or patients. In five Phase IIa,
placebo-controlled trials using intravenous administration, tezampanel
demonstrated proof of concept in multiple pain models. In one placebo and
active-controlled clinical trial in patients with acute migraine, the
compound achieved statistical significance in all primary and secondary
endpoints traditionally required for regulatory approval. These endpoints
included pain relief at two hours, pain-free at two hours and relief of
nausea, photophobia and phonophobia.
About AK Receptor Antagonists
AMPA/kainate (AK) receptors are part of the glutamate biological
pathway that transmits pain signals to the brain. In addition, these
receptors play a critical role in the development of central sensitization
phenomena -- a key component of many pain syndromes, including migraine and
persistent pain states such as chronic neuropathic pain. AK receptor
antagonists selectively bind to certain AK receptors to block transmission
of pain signals mediated through the activation of a subtype of glutamate
receptors. Because they do not bind to opioid receptors, directly bind to
serotonin receptors or constrict blood vessels, the safety profile of AK
antagonists may offer important advantages over existing drugs to treat
migraine and other chronic pain conditions.
About Migraine
Migraine is a painful neurological condition characterized by an
intense and disabling episodic headache. According to the National Headache
Foundation, an estimated 30 million people in the U.S. suffer fr
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SOURCE TorreyPines Therapeutics, Inc.
 Copyright©2007 PR Newswire. | |
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