Winston Laboratories, Inc. Submits NDA for CIVANEX® (Civamide Cream) for Treatment of Osteoarthritis
07 Julio 2010 - 7:00AM
Business Wire
Winston Laboratories, Inc., a wholly-owned subsidiary of Winston
Pharmaceuticals, Inc. (“Winston”) (OTC PINK: WPHM), a
pharmaceutical company focused on developing and commercializing
novel pain management therapies, announced that it has submitted a
new drug application (NDA) with the U.S. Food and Drug
Administration (FDA) for approval to market its civamide
(zucapsaicin) 0.075% cream, CIVANEX®, for the treatment of signs
and symptoms of osteoarthritis of the knee. Winston anticipates
that the application will be subject to a standard review with a
Prescription Drug User Fee Act (PDUFA) date in the second half of
2011.
The NDA submission is supported by randomized, double-blind,
well-controlled clinical studies of CIVANEX® in more than 1,200
patients. Clinical trials show that CIVANEX®-treated patients
experienced a statistically significant reduction in the Western
Ontario and McMaster Universities Arthritis Index (“WOMAC”) Pain
scale, the WOMAC Physical Function Subscale and a Patient Global
Evaluation over a 12-week treatment period, relative to those in a
lower dose control group. Since there is no systemic absorption of
civamide, CIVANEX® can be administered either as a monotherapy or
in combination with other systemic pain relief medications. The
most common adverse reactions associated with CIVANEX® were
transient burning or stinging at the application site.
“We are pleased to have submitted our NDA for CIVANEX® in the
United States,” said Joel E. Bernstein, M.D., President and CEO of
Winston. “In addition to this regulatory milestone, we have ongoing
reviews of our marketing authorization application (MAA) in the
European Union and our new drug submission (NDS) in Canada. We
anticipate a decision on the NDS in the third quarter of 2010, and
eagerly anticipate the commercial launch of CIVANEX® in both North
America and the European Union.”
About Osteoarthritis
Osteoarthritis is the most common form of arthritis, affecting
more than 21 million Americans, mainly adults over age 45. Women
are more susceptible to this condition. Osteoarthritis affects the
fingers, spinal column and weight-bearing joints such as the hips,
knees and feet. The main symptom of osteoarthritis is pain, the
degree of which ranges from mildly inconvenient to debilitating. By
2030, an estimated 67 million Americans aged 18 years or older will
have doctor-diagnosed arthritis. For some patients with
osteoarthritis, relief of mild-to-moderate joint pain is afforded
by acetaminophen (e.g. Tylenol®) or a nonsteroidal
anti-inflammatory drug (NSAID), such as ibuprofen (e.g. Motrin®,
Advil®, etc.), but even these OTC medications have systemic side
effects and drug interactions. A topical medication without
systemic absorption, which can be utilized as either monotherapy or
adjunctive therapy absent risk of systemic side effects or drug
interactions, would be quite advantageous. Alternate approaches
include intra-articular therapies such as hyaluronic acid and
glucocorticoids.
About Winston Pharmaceuticals
Winston is a pharmaceutical company focused on pain control
which is developing products for large pain control markets, as
well as for niche markets, where there are still significant unmet
needs for pain management options with improved efficacy, safety,
and tolerability profiles. Winston's late stage product candidates
include osteo- and rheumatoid arthritis, neuropathic pain, episodic
cluster headache, chronic daily headache, and pain and inflammation
in inflammatory bowel disease.
About Civamide
Civamide (zucapsaicin; chemical name:
cis-8-methyl-N-vanillyl-6-nonenamide) is a patented, synthetically
produced TRPV-1 receptor modulator, which selectively depresses the
activity of the type-C pain fibers. Civamide causes an initial
release of the neuropeptides, substance P (SP) and calcitonin-gene
related peptide (CGRP). Pain transmission and inflammation is then
diminished by the subsequent depletion of SP and CGRP from the
neuron, coupled with suppression of the synthesis and transport of
neuropeptides along the neuron.
This press release contains “forward-looking statements,” as
that term is defined under the Private Securities Litigation Reform
Act of 1995 (PSLRA), regarding product development efforts and
other non-historical facts about expectations, beliefs or
intentions regarding the business, technologies and products,
financial condition, strategies or prospects. Many factors could
cause actual activities or results to differ materially from the
activities and results anticipated in forward-looking statements.
These factors include those described in our filings with the
Securities and Exchange Commission, as well as risks inherent in
funding, developing and obtaining regulatory approvals of new,
commercially-viable and competitive products and treatments,
including the risks that any products under development may fail,
may not achieve the expected results or effectiveness and may not
generate data that would support the approval or marketing of
products for the ailments being studied or for other ailments. In
addition, forward-looking statements also may be adversely affected
by general market factors, competitive product development, product
availability, federal and state regulations and legislation, the
regulatory process for new products and indications, manufacturing
issues that may arise, patent positions and litigation, among other
factors. We do not undertake any obligation to update
forward-looking statements. We intend that all forward-looking
statements be subject to the safe-harbor provisions of the
PSLRA.
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