FDA Accepts NDA Filing for Retigabine
December 30 2009 - 8:00AM
PR Newswire (US)
MAA successfully validated by EMEA ALISO VIEJO, Calif., Dec. 30
/PRNewswire-FirstCall/ -- Valeant Pharmaceuticals International
(NYSE:VRX) today announced that the U.S. Food and Drug
Administration (FDA) has accepted for review the New Drug
Application (NDA) seeking marketing approval for the
investigational drug retigabine, a neuronal potassium channel
opener for the adjunctive treatment for adult epilepsy patients
with partial-onset seizures. In addition, the European Medicines
Agency (EMEA) confirmed on November 17, 2009 that the MAA was
successfully validated thus enabling the MAA review to commence.
The filings were submitted on October 30, 2009. About Retigabine
Retigabine is a neuronal potassium channel opener currently in
late-stage development as an adjunctive treatment for adult
patients with partial-onset seizures. In Phase III epilepsy trials,
retigabine reduced seizure rates compared to patients taking
placebo. The most common adverse reactions (incidence greater than
or equal to 5% and twice placebo) across all completed trials to
date are dizziness, fatigue, confusional state, vertigo, tremor,
coordination abnormal, diplopia (double vision), disturbance in
attention, asthenia (weakness), and visual blurring. Retigabine
Important Note As an investigational drug, retigabine has not been
found by the Food and Drug Administration (FDA) or any other
regulatory agency to be safe or effective in the treatment of any
disease or illness. It may not be commercialized in the United
States unless and until the FDA has approved a NDA. Similar
restrictions apply in other countries. Collaboration Agreement with
GlaxoSmithKline Valeant has a worldwide License and Collaboration
Agreement with GlaxoSmithKline (NYSE:GSK), to develop and
commercialize retigabine. Valeant will collaborate with GSK on the
development and marketing of retigabine in the United States,
Australia, New Zealand, Canada and Puerto Rico (Collaboration
Territory) and GSK has an exclusive license to develop and
commercialize retigabine in countries outside of the Collaboration
Territory and certain backup compounds to retigabine worldwide.
About Valeant Valeant Pharmaceuticals International (NYSE:VRX) is a
multinational specialty pharmaceutical company that develops,
manufactures and markets a broad range of pharmaceutical products
primarily in the areas of neurology and dermatology. More
information about Valeant can be found at http://www.valeant.com/.
(Logo: http://www.newscom.com/cgi-bin/prnh/20081125/VALEANTLOGO)
Contact: Laurie W. Little Valeant Pharmaceuticals 949-461-6002
http://www.newscom.com/cgi-bin/prnh/20081125/VALEANTLOGO
http://photoarchive.ap.org/ DATASOURCE: Valeant Pharmaceuticals
International CONTACT: Laurie W. Little of Valeant Pharmaceuticals,
+1-949-461-6002, Web Site: http://www.valeant.com/
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