For most of the 20th century, pharmaceutical intellectual property was a single-act play. You discovered a molecule, filed a composition-of-matter
The Platform Technology Moat: Why the Single-Molecule Patent No Longer Wins the IP War Read Post »
Every year, billions of dollars in generic-entry forecasts are built on a single assumption: that the patent expiry date listed
Patent Term Extensions: The Most Misunderstood Dates in Pharma Read Post »
The moment a generic competitor files an Abbreviated New Drug Application, the brand manufacturer’s revenue clock starts ticking. But the
The executives who built careers navigating Hatch-Waxman—who internalized the 30-month stay, the Paragraph IV certification, the 180-day first-filer exclusivity—carry a
Why Small Molecule Thinking Will Fail You in the Biosimilar Era Read Post »
The average cost to develop a new drug reached $2.23 billion in 2024, with an expected ROI of just 5.9%.
Paragraph IV Is Pharma’s Most Profitable R&D Strategy Read Post »
Quick Summary: Obviousness-type double patenting (ODP) is a judicially created doctrine that prevents patent holders from stretching exclusivity by obtaining
The Double Patenting Trap: How Pharma Brands Accidentally Invalidate Their Own Moats Read Post »
The answer to whether you should use PAT-INFORMED to find drug patent loss-of-exclusivity dates depends entirely on who you are,
PAT-INFORMED for Drug LOE Dates: What Procurement Agencies and Analysts Get Wrong Read Post »
Between September 2023 and May 2025, the Federal Trade Commission challenged more than 600 patent listings in the FDA’s Orange
Orange Book Delisting Wave: What the FTC Crackdown Means for Your Pipeline Read Post »
When a patient types “Is there a cheaper alternative to Eliquis?” into ChatGPT, they expect an accurate, up-to-date answer. What
Do LLMs Recommend Branded Drugs More Often Than Generics? Read Post »
Sign in or create a free account to read this DrugPatentWatch article
