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U.S. biosimilars – The courts interpret BCPIA steps
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Journal of Bioanalysis & Biomedicine

ISSN: 1948-593X

Open Access

U.S. biosimilars – The courts interpret BCPIA steps


4th International Conference and Exhibition on Biologics & Biosimilars

October 26-28, 2015 Baltimore, USA

Denise M Kettelberger

Sunstein Kann Murphy & Timbers LLP, USA

Scientific Tracks Abstracts: J Bioanal Biomed

Abstract :

SANDOZ filed an aBLA seeking the first approval of a U.S. biosimilar, a filgrastim product. AMGENâ??s Neupogen?® was the reference product. U.S. biosimilar companies closely followed progress of the first product to use the U.S. Biosimilar law (Biologics Price Control and Innovation Act. Surprisingly, SANDOZ did not proceed through the multi-step aBLA pathway of the BPCIAâ??s patent dispute resolution system, choosing instead to notify AMGEN of the aBLA filing, expected approval date, and intended launch. Instead of the BCPIAâ??s elaborate process for confidential information exchange and resolution of patent disputes, SANDOZ opted out of the process and did not provide AMGEN with its aBLA application. Because SANDOZ failed to provide its application and manufacturing process, AMGEN was entitled to sue SANDOZ for patent infringement under non-compliance sanctions provided in BCPIA steps. AMGEN sued SANDOZ for unfair competition; conversion; and infringement of AMGENâ??s patents. The, District Court dismissed unfair competition and conversion clams due to its interpretation of BPCIA, finding SANDOZ did not act unlawfully. On appeal to the Federal Circuit, the BCPIA was again interpreted in Amgen v. Sandoz, decided July 21, 2015. The Court reviewed SANDOZâ??s failure to comply with the first step: applicant â??shall provideâ? its application and manufacturing process; 180 day notice of intent to market; and whether BCPIA steps are optional or mandatory. The Court found the BCPIA steps to be required when the aBLA path is chosen, but not when the applicant chooses not to use the BCPIA. Federal Circuit en banc review was requested.

Biography :

Denise M Kettelberger received her PhD from the University of Maryland School of Medicine, completed Postdoctoral studies at Baylor College of Medicine with Bert O’Malley, and moved into patent law as DNA products advanced, and joined Pravel, Gambrell as a patent agent. A former Merchant & Gould partner, she recently joined Sunstein Kann Murphy & Timbers LLP, a premier patent firm in Boston. Active in the American Intellectual Property Law Association, she is a frequent speaker on biotechnology patent issues.

Email: dkettelberger@sunsteinlaw.com

Google Scholar citation report
Citations: 3099

Journal of Bioanalysis & Biomedicine received 3099 citations as per Google Scholar report

Journal of Bioanalysis & Biomedicine peer review process verified at publons

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