Statement by Ralph G. Neas, President and CEO, Generic Pharmaceutical Association, on FDA’s Acceptance of Sandoz Biologics License Application for Filgrastim Under the New Biosimilar Pathway
Published Online: Thursday, July 24, 2014
“For the first time, the FDA has accepted a filing for an approval of a biosimilar drug, a major step toward access for Americans to safe, effective alternatives to costly brand biologic medicines.
Biosimilars have been successfully used in Europe and other markets for years. Filgrastim’s filing acceptance moves us closer to the day when U.S. patients that currently must rely on costly brand biologics for treatment will have more choices for the medicine that they need.
This approval represents a new frontier — not only for patients, but for our nation’s health system. Express Scripts projects that the United States would save $250 billion between 2014 and 2024 if filgrastim and 10 other biosimilars would enter the market.
We look forward to the integration of biosimilar therapies into the American health system, and witnessing the realization of the transformative potential of these innovative therapies.”