The Analyst Report That Took Three Weeks Should Have Taken Three Hours — Here’s the Bottleneck
A comprehensive freedom-to-operate analysis for a pharmaceutical asset takes four to twelve weeks and costs $50,000 to $200,000 in legal […]
A comprehensive freedom-to-operate analysis for a pharmaceutical asset takes four to twelve weeks and costs $50,000 to $200,000 in legal […]
On September 9, 2026, Bristol-Myers Squibb’s five-year new chemical entity (NCE) exclusivity for Sotyktu (deucravacitinib) reaches its four-year mark. That
On October 8, 2025, the U.S. Patent and Trademark Office quietly admitted something the patent search industry had been saying
Stop Searching Patents. Start Asking Them Questions. Read Post »
The Short Answer A pharmaceutical patent lawsuit becomes public the moment it is entered on a federal docket. Nobody has
Eight of Teva’s nine Copaxone patents expired in May 2014. The first FDA-approved generic, Sandoz’s Glatopa, didn’t reach a pharmacy
The Three-Clock Problem: Why Patent Expiration Dates Don’t Predict Generic Launch Dates Read Post »
In March 2022, the first generic version of Bristol Myers Squibb’s cancer drug Revlimid reached U.S. pharmacies. It launched at
GSK’s Advair lost its core patent in 2010. Fourteen years later the inhaler was still bringing in £863 million —
The Blockbuster’s Real Patent Is the Weak One Nobody Challenged 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
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