Litigation

Litigation

Spotlight On: Rituxan® (rituximab) / Truxima® (rituximab-abbs)
Spotlight On: Rituxan® (rituximab) / Truxima® (rituximab-abbs) April M. Breyer Menon; Corinne E. Atton; Joyce L. Nadipuram; Robert S. Schwartz, Ph.D. November 30, 2018
VIDEO: The FDA’s Biosimilar Action Plan
VIDEO: The FDA’s Biosimilar Action Plan Ha Kung Wong August 30, 2018
Biosimilars and the Biologics Price Competition and Innovation Act (BPCIA)
Biosimilars and the Biologics Price Competition and Innovation Act (BPCIA) Michael Enzo Furrow, Ph.D.; Whitney L. Meier July 31, 2018
Venable Fitzpatrick’s BiologicsHQ Monthly Injection – May 2018
Venable Fitzpatrick’s BiologicsHQ Monthly Injection – May 2018 April M. Breyer Menon; Joseph K. Yarsky; Corinne E. Atton; Robert S. Schwartz, Ph.D. June 8, 2018
WEBINAR: Update on Biologic Drug IPRs: Lessons Learned Corinne E. Atton; Whitney L. Meier; Robert S. Schwartz, Ph.D. February 22, 2018

Methodology

Information contained in the Venable Fitzpatrick 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 Fitzpatrick BiologicsHQ database.

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