Strong IP Doesn’t Win in Court. Enforceable IP Does.
In May 2023, the Supreme Court unanimously threw out two Amgen patents that, on their face, covered every antibody that […]
Strong IP Doesn’t Win in Court. Enforceable IP Does. Read Post »
In May 2023, the Supreme Court unanimously threw out two Amgen patents that, on their face, covered every antibody that […]
Strong IP Doesn’t Win in Court. Enforceable IP Does. Read Post »
Nine months after Humira lost U.S. exclusivity, biosimilars held four percent of the market. AbbVie’s Humira still controlled ninety-six percent
In 2023, Mylan filed an inter partes review against Novo Nordisk’s U.S. Patent No. 8,536,122, the compound patent covering semaglutide,
The Prior Art Edge: Why Search Quality Beats Legal Firepower in Drug Patent Litigation Read Post »
On November 30, 2011, Ranbaxy Laboratories was supposed to be the only company selling a generic version of Lipitor. It
The Authorized Generic That Beats the Patent Cliff to Market Read Post »
The Short Answer A patent’s presence in the FDA Orange Book proves it was submitted and accepted for listing. It
The Short Answer: Under FDA’s interpretation of the Hatch-Waxman Act, “first applicant” status on a Paragraph IV certification is determined
One Day Late, Nine Figures Short: What Being the Second First-to-File Actually Costs Read Post »
In March 2002, Teva filed an ANDA for generic carvedilol targeting a patent that would not expire for five more
On October 31, 2025, the director of the U.S. Patent and Trademark Office denied institution of thirteen inter partes review
The Myth of the Stable Drug Patent: Why IPRs Change the Game Overnight Read Post »
A Paragraph IV certification feels like an ambush when a generic company files it. It rarely is one for the
Predictable by Design: How Brands Outmaneuver Your Paragraph IV Strategy Read Post »
Sign in or create a free account to read this DrugPatentWatch article