Mylan's Matrix Receives Tentative FDA Approval Under PEPFAR for Efavirenz, Lamivudine and Tenofovir Disoproxil Fumarate Tablets
16 Setembro 2009 - 8:30AM
PR Newswire (US)
PITTSBURGH, Sept. 16 /PRNewswire-FirstCall/ -- Mylan Inc.
(NASDAQ:MYL) today announced that its privately held Indian
subsidiary, Matrix Laboratories Limited, has received tentative
approval from the U.S. Food and Drug Administration (FDA) under the
President's Emergency Plan for AIDS Relief (PEPFAR) for its New
Drug Application (NDA) for Efavirenz, Lamivudine and Tenofovir
Disoproxil Fumarate Tablets, 600 mg/300 mg/300 mg. Mylan's product
represents the first-ever fixed-dose combination of Efavirenz,
Lamivudine and Tenofovir Disoproxil Fumarate and now provides
Matrix with numerous Tenofovir combination product opportunities.
This new drug adds to the Matrix portfolio of important treatments
for HIV/AIDS. The product may be used for either first- or
second-line treatment in adults. People use second-line therapies
if and when they develop resistance to initially prescribed
treatments. Mylan President Heather Bresch said: "This product
represents yet another important advance in our continuing fight
against the global epidemic of HIV/AIDS. By combining three
antiretroviral (ARV) products into a once-daily dose, we can
dramatically improve the quality of care for people living with
HIV/AIDS in emerging markets. Lower pill burden also increases the
likelihood that patients adhere to treatment. This innovation also
adds another affordable option to our large and rapidly growing
portfolio of life-sustaining ARV products." The FDA's tentative
approval under PEPFAR means that Matrix's product meets all of the
agency's manufacturing quality, safety and efficacy standards.
Although existing patents or exclusivity prevent its marketing in
the U.S., the product will be eligible for purchase outside the
U.S. in many developing countries. Matrix's wide range of ARV
products includes active pharmaceutical ingredients and first- and
second-line finished doses. The company's emphasis on producing
affordable products has allowed it to drive down the average annual
cost per patient of effective therapies. Approximately 30% of
HIV/AIDS patients in developing countries who are receiving
treatment depend on Matrix ARV products. Mylan Inc. ranks among the
leading generic and specialty pharmaceutical companies in the world
and provides products to customers in more than 140 countries and
territories. The company maintains one of the industry's broadest
and highest quality product portfolios supported by a robust
product pipeline; operates the world's third largest active
pharmaceutical ingredient manufacturer; and runs a specialty
business focused on respiratory and allergy therapies. For more
information, please visit http://www.mylan.com/. DATASOURCE: Mylan
Inc. CONTACT: Michael Laffin (Media), +1-724-514-1968, or Dan
Crookshank (Investors), +1-724-514-1813, both of Mylan Inc. Web
Site: http://www.mylan.com/
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