How Can Biosimilars Make Headway in the U.S. Market?

by April Breyer Menon | Jun 26, 2019

Venable partner Ha Kung Wong spoke at ISPOR’s annual conference as part of a panel that discussed the biosimilar market in the US. As a follow-up to that presentation, Ha Kung participated in a Q&A for Biosimilar Development, including providing thoughts...

Comparing the Economics of Biosimilars and Generics

by April Breyer Menon | Jun 25, 2019

Venable partner Ha Kung Wong spoke at the ACI 10th Summit on Biosimilars as part of a panel that reviewed the economics of biosimilars and generic drugs. Highlights from his presentation comparing biosimilar markets in Europe and the United States and his take-home...

New Bill Would Reshape Drug Patent Cases in Uncertain Ways

by April Breyer Menon | Jun 14, 2019

Venable partner Ha Kung Wong commented on the Terminating the Extension of Rights Misappropriated Act, or TERM Act, H.R. 3199, as part of the Law360 article “New Bill Would Reshape Drug Patent Cases in Uncertain Ways,” available here. The TERM Act was...

Venable’s BiologicsHQ Monthly Injection – May 2019

by April Breyer Menon | Jun 6, 2019

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Biosimilar Experts Give Highlights of US Uptake Issues

by April Breyer Menon | May 23, 2019

Venable partner Ha Kung Wong spoke at the ISPOR 2019 annual meeting as part of a panel that reviewed the current state of the biosimilar market and challenges to biosimilar uptake in the U.S. His comments on pending Congressional action relating to the Purple Book,...

Venable’s BiologicsHQ Monthly Injection – April 2019

by April Breyer Menon | May 7, 2019

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Methodology

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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