In an article for Biosimilar Development, Ha Kung Wong and Erica Norey discuss the potential impact of authorized biologics on the developing biosimilars market. The article draws upon experience with authorized generics in the small molecule drug market and discusses the role interchangeability designations for biosimilars could play in prompting authorized biologic development.
Read the full article here.
Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.
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