Genentech, together with City of Hope, has filed a new complaint for patent infringement against Pfizer over PF-06439535, Pfizer’s proposed bevacizumab biosimilar referencing Genentech’s Avastin.
Genentech, together with City of Hope, has filed a new complaint for patent infringement against Pfizer over PF-06439535, Pfizer’s proposed bevacizumab biosimilar referencing Genentech’s Avastin.
The complaint, filed in the United States District Court for the District of Delaware, claims that Pfizer has infringed on 22 patents related to bevacizumab and comes after Pfizer submitted an abbreviated Biologics License Application (aBLA) for the product to the FDA.
According to the complaint, Pfizer had 20 days to provide Genentech with its aBLA after regulatory submission, and the biosimilar developer was also required to provide “other information” related to manufacturing of the proposed product. This early disclosure under the terms of the Biologics Price Competition and Innovation Act (BPCIA), says Genentech, is important for the undertaking of preliminary injunction proceedings.
However, according to the complaint, Pfizer “ignored this targeted request” for information and “took the position that producing only portions of its aBLA alone was sufficient under the statute.” In September of last year, Pfizer produced “only portions” of the aBLA and did not give Genentech the other information that it sought.
Despite Genentech’s protests, Pfizer has indicated that its production satisfied statutory obligations, leading to an exchange of correspondence between the drug makers over the following months.
In March 2019, Pfizer accepted and agreed on the patents, for which Genentech provided infringement contentions, that would be the subject of a patent infringement action under the BPCIA.
Some of the patents listed in the complaint have already expired, but Genentech contends that, prior to expiry, Pfizer infringed these patents by making its proposed biosimilar in the United States in a manner not covered by safe harbor.
Genentech has requested a trial by jury. It has asked that the court find that Pfizer has infringed on its asserted patents and will infringe on those patents by making, using, or selling its product, and it also asks that the court find that Pfizer failed to provide adequate information as required under law. Genentech seeks damages, including a preliminary and a permanent injunction against infringement of the patents in question.
President Trump Signs Executive Order to Bring Down Drug Prices
April 16th 2025To help bring down sky-high drug prices, President Donald Trump signed an executive order pushing for faster biosimilar development, more transparency, and tougher rules on pharmacy benefit managers—aiming to save billions and make meds more affordable for everyone.
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
Experts Pressure Congress to Remove Roadblocks for Biosimilars
April 12th 2025Lawmakers and expert witnesses emphasized the potential of biosimilars to lower health care costs by overcoming barriers like pharmacy benefit manager practices, limited awareness, and regulatory delays to improve access and competition in chronic disease management during a recent congressional hearing.
Decoding the Patent Puzzle: Navigating the Legal Landscape of Biosimilars
March 17th 2024On this episode of Not So Different, Ha Kung Wong, JD, an intellectual patent attorney and partner at Venable LLP, details the confusing landscape that is the US patent system and how it can be improved to help companies overcome barriers to biosimilar competition.
Review Calls for Path to Global Harmonization of Biosimilar Development Regulations
March 17th 2025Global biosimilar regulatory harmonization will be needed to reduce development costs and improve patient access, despite challenges posed by differing national requirements and regulatory frameworks, according to review authors.
Biosimilar Cases to Watch: Prolia/Xgeva and Denosumab Competitors
March 11th 2025The denosumab biosimilar market is poised for disruption with 3 FDA-approved biosimilars, at least 5 awaiting approval, and launches anticipated to start in May 2025, while ongoing patent litigation continues to shape the competitive landscape.