Skip to main content
· 4/4/1997

Glaxo, Inc., and Glaxo Group Limited v. Novopharm, Ltd.

Citations

  • 110 F.3d 1562
  • 42 U.S.P.Q. 2d (BNA) 1257
  • 1997 U.S. App. LEXIS 6472
  • 1997 WL 156592

How courts have described this case

Verbatim parenthetical descriptions written by other courts when citing this decision. Ranked by citation-network relevance.

  • holding that the patentee still carries the burden to prove that the product a generic drug maker ultimately will put on the market would likely infringe the patent
  • holding that, “where the subject matter is a compound capable of existing in multiple crystalline forms, or mixtures thereof, the ultimate question of infringement is not so simple”
  • noting that district court “properly considered the ANDA itself, the materials submitted by Novopharm to the FDA, and other pertinent evidence” in conducting its infringement analysis
  • noting that § 271(e) changes the result in Roche
  • describing infringement actions under 35 U.S.C. § 271(e)(2), prior to a launch and “based solely upon the filing of an ANDA” and “focused on the product that is ultimately to be sold”
  • “The relevant inquiry is whether patentee has proven by a preponderance of the evidence that the alleged infringer will likely market an infringing product.”

Source: CourtListener parenthetical corpus (CC0).

Judges: Lourie, Clevenger, Schall

Read full opinion on CourtListener

Sourced from CourtListener / Free Law Project (CC0).

This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.