NDA
for Once-Daily ADHD Patch Accepted by Food and Drug Administration Miami, FL, August
27, 2002 -- Noven Pharmaceuticals, Inc. (NASDAQ: NOVN) today announced
that its New Drug Application (NDA) for once-daily MethyPatch®
(transdermal methylphenidate system) has been accepted for filing with
the U.S. Food and Drug Administration (FDA). Noven submitted the
NDA on June 27, 2002 seeking approval to market MethyPatch for the treatment
of Attention Deficit Hyperactivity Disorder (ADHD). Acceptance for filing
occurs automatically 60 days after submission of an NDA, unless the FDA
indicates during the 60-day period that the application is not sufficiently
complete to permit a substantive review. MethyPatch combines
methylphenidate an established ADHD therapy with Noven's
patented DOT Matrix patch technology, which is the delivery platform
underlying Noven's Vivelle-Dot® and CombiPatch®
hormone replacement patches. DOT Matrix technology permits Noven to deliver
predictable therapeutic doses of a range of prescription therapies through
discreet, comfortable and adherent patches that are well suited to active
lifestyles. ADHD is characterized
by developmentally inappropriate impulsivity, inattention and hyperactivity.
ADHD affects 3% to 5% of school-aged children, and an estimated 1.5 million
children are currently on medication to treat this disorder. All presently
approved ADHD medications are delivered orally. About
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