BASEL, SWITZERLAND
AND MIAMI, FL. - August 2, 2001 - Novartis Pharma AG and Noven Pharmaceuticals,
Inc. (Nasdaq: NOVN) announced today that Novartis Pharma has applied for
marketing authorization for Estradot® (transdermal 17-beta
estradiol) in the European Union under the Mutual Recognition Procedure,
which would give the drug marketing authorization in all European Union
Member States. Estradot was recently approved in the Netherlands, which
will act as the Reference Member State, for the treatment of menopausal
symptoms and the prevention of post-menopausal osteoporosis. Estradot offers patients
a convenient, comfortable and cosmetically attractive means of administering
hormone replacement therapy. An advance over older technology, Estradot
provides improved adhesion, reduced skin irritation and is almost invisible
on the skin. "Estradot further
consolidates our strong global portfolio in Women's Health products,"
said Thomas Ebeling, CEO, Novartis Pharma. "Given its success in
the U.S., we have high aspirations for Estradot in Europe, where hormone
replacement patches are extremely popular." Robert C. Strauss,
Noven's President, CEO and Chairman, added, "We are pleased that
Novartis continues to advance the European approval process for Estradot,
which underscores Novartis' continuing commitment to our advanced transdermal
products and technologies." Developed and manufactured
by Noven, Estradot is licensed by Novartis in all countries outside the
US and Japan. In the US, Novartis and Noven market the product as Vivelle-Dot™
through their jointly-owned Women's Health company, Vivelle Ventures LLC
(also known as Novogyne Pharmaceuticals). About Hormone
Replacement Therapy The forgoing press
release contains forward-looking statements which can be identified by
terminology such as "applied", "would", "aspirations",
"estimated" or similar expressions. Such forward looking statements
involve known and unknown risks, uncertainties and other factors that
may cause actual results to be materially different from any future results,
performance or achievements expressed or implied by such statements. The
successful commercialization of Estradot can be affected by, amongst other
things, uncertainties relating to product development, regulatory actions
or delays or government regulation generally, the ability to obtain or
maintain patent or other proprietary intellectual property protection,
competition in general as well as factors discussed in the Form 20-F filed
by Novartis AG, and the Form 10-K and Form 10-Qs filed by Noven, with
the Securities and Exchange Commission. About Novartis About Noven Investor &
Media Contact: Copyright © 2001 Noven Pharmaceuticals, Inc. All rights reserved. |