· 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 CourtListenerSourced from CourtListener / Free Law Project (CC0).
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