Teva Pharmaceuticals USA, Inc. v. Sandoz, Inc. explained

Litigants:Teva Pharmaceuticals USA, Inc. v. Sandoz, Inc.
Arguedate:October 15
Argueyear:2014
Decidedate:January 20
Decideyear:2015
Fullname:Teva Pharmaceuticals USA, Inc. v. Sandoz, Inc.
Usvol:574
Uspage:318
Docket:13-854
Parallelcitations:135 S. Ct. 831; 190 L. Ed. 2d 719; 2014 U.S. LEXIS 4897; 83 U.S.L.W. 4055; 113 U.S.P.Q.2d 1269
Prior:810 F. Supp. 2d 578 (S.D.N.Y. 2011); 876 F. Supp. 2d 295 (S.D.N.Y. 2012); affirmed in part, reversed in part, and remanded, 723 F.3d 1363 (Fed. Cir. 2013); stay denied, 572 U.S. 1301 (2014); cert. granted, 572 U.S. 1033 (2014)
Subsequent:On remand, 789 F.3d 1335 (Fed. Cir. 2015)
Holding:When reviewing a district court’s resolution of subsidiary factual matters made in the course of its construction of a patent claim, the Federal Circuit must apply a "clear error," not a de novo, standard of review.
Majority:Breyer
Joinmajority:Roberts, Scalia, Kennedy, Ginsburg, Sotomayor, Kagan
Dissent:Thomas
Joindissent:Alito
Lawsapplied:F.R.C.P. 52(a)(6)

Teva Pharmaceuticals USA, Inc. v. Sandoz, Inc., 574 U.S. 318 (2015),[1] is a patent case of the Supreme Court of the United States regarding the Copaxone patent. The Court held that, when reviewing a district court’s resolution of subsidiary factual matters made in the course of its construction of a patent claim, the Federal Circuit must apply a "clear error," not a de novo, standard of review.[1]

Facts and procedural history

The case originated in the Southern District of New York, where Sandoz sued to invalidate Teva's patent on a drug for the treatment of multiple sclerosis. In the Markman hearing, Sandoz argued that a claim was fatally indefinite for failing to identify which of three possible meanings a particular claim term, related to the molecular weight of a component of the drug, should be interpreted to have. The district court judge held that the claim term was definite, and that a "person of ordinary skill in the art" would interpret the term "molecular weight" to mean the "peak average molecular weight", that is, the weight of the molecule most prevalent in the mixture.[2] In doing so, the judge relied in part on expert witness testimony.

Sandoz appealed to the Federal Circuit, which reviewed the claim under a 'de novo' standard, decided that the claim term was fatally indefinite, and hence that the patent was invalid.[3]

Teva appealed to the US Supreme Court and won.

Notes and References

  1. .
  2. Teva Pharmaceuticals USA, Inc. v. Sandoz, Inc. . 810 . F. Supp. 2d . 578 . . 2011 . https://www.leagle.com/decision/infdco20110831a36 . July 4, 2018.
  3. Teva Pharmaceuticals USA, Inc. v. Sandoz, Inc. . 723 . F.3d . 1363 . . 2013 . https://www.leagle.com/decision/infco20130726110 . July 4, 2018.