Shire Development, LLC v. Watson Pharmaceuticals, Inc.

848 F.3d 981, 121 U.S.P.Q. 2d (BNA) 1509, 2017 WL 541013, 2017 U.S. App. LEXIS 2393
CourtCourt of Appeals for the Federal Circuit
DecidedFebruary 10, 2017
Docket2016-1785
StatusPublished
Cited by5 cases

This text of 848 F.3d 981 (Shire Development, LLC v. Watson Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Shire Development, LLC v. Watson Pharmaceuticals, Inc., 848 F.3d 981, 121 U.S.P.Q. 2d (BNA) 1509, 2017 WL 541013, 2017 U.S. App. LEXIS 2393 (Fed. Cir. 2017).

Opinion

HUGHES, Circuit Judge.

Plaintiffs (collectively, Shire) sued Defendants (collectively, Watson) for infringing claims 1 and 3 of U.S. Patent No. 6,773,720 by filing Abbreviated New Drug Application No. 203817 with the Food and Drug Administration seeking to market a generic version of Shire’s mesalamine drug, LIALDA®. Because Watson’s ANDA Product does not satisfy the Mar-kush group requirements in claim 1(b), we reverse and remand with instructions to enter judgment of non-infringement.

*983 I

A

The ’720 patent is directed to a controlled-release oral pharmaceutical composition of mesalamine (also known as mesa-lazine or 5-amino-salicylic acid) used to treat certain inflammatory bowel diseases. Shire Dev., LLC v. Watson Pharm., Inc., 787 F.3d 1359, 1361 (Fed. Cir. 2015) (2015 Decision). That composition includes the mesalamine active ingredient; an inner, li-pophilic matrix; an outer, hydrophilic matrix; and other optional excipients. ’720 patent col. 2 ll. 36-44.

When a matrix is hydrophilic, it “has an affinity for water” and therefore “readily dissolves in” it. 2015 Decision, 787 F.3d at 1362 n.1; see Shire Dev. LLC v. Watson Pharm., Inc., No. 12-60862-CIV, 2016 WL 1258885, at *6 (S.D. Fla. Mar. 28, 2016) (2016 Trial Decision) (noting the parties’ stipulated-to definition of “hydrophilic” as “having an affinity to water”). Conversely, when a matrix is lipophilic, it “has an affinity for lipids” and therefore “resists dissolving in water.” 2015 Decision, 787 F.3d at 1362 n.1; see id. at 1365 (noting the parties’ stipulated-to definition of “lipophilic” as “poor affinity towards aqueous fluids”).

Shire asserts claims 1 and 3 of the ’720 patent. In relevant part, claim 1 reads:

1. Controlled-release oral pharmaceutical compositions containing as an active ingredient 5-amino-salicylic acid, comprising:
a)an inner lipophilic matrix consisting of substances selected from the group consisting of unsaturated and/or hydrogenated fatty acid, salts, esters or amides thereof, fatty acid mono-, di- or triglycerids, waxes, cer-amides, and cholesterol derivatives with melting points below 90° C., and wherein the active ingredient is dispersed both in said [sic] the lipophilic matrix and in the hydrophilic matrix;
b) an outer hydrophilic matrix wherein the lipophilic matrix is dispersed, and said outer hydrophilic matrix consists of compounds selected from the group consisting of polymers or copolymers of acrylic or methacrylic acid, alkylvinyl polymers, hydroxy-alkyl celluloses, carboxyalkyl cellulos-es, polysaccharides, dextrins, pectins, starches and derivatives, alginic acid, and natural or synthetic gums;
c) optionally other excipients....

’720 patent col. 6 ll. 7-30 (emphases added). Dependent claim 3 limits the composition to “the form of tablets, capsules, [or] mintablets [sic].” Id. col. 6 ll. 34-35.

B

In 2013, following a bench trial, the district court rejected Watson’s invalidity arguments that the ’720 patent lacked written description and enablement, ,and held that Watson infringed claims 1 and 3. Shire Dev. LLC v. Watson Pharm., Inc., No. 12-60862-CIV, 2013 WL 1912208, at *16 (S.D. Fla. May 9, 2013) (2013 Trial Decision).

On appeal, and again after remand from the Supreme Court, we held that the ’720 patent matrices are “defined by mutually exclusive spatial characteristics — one inner, one outer — and mutually exclusive compositional characteristics — one hydro-philic, one lipophilic.” 2015 Decision, 787 F.3d at 1366, remanded by — U.S. -, 135 S.Ct. 1174, 191 L.Ed.2d 130 (2015), granting cert. to and vacating 746 F.3d 1326 (Fed. Cir. 2014). Thus we concluded that a “matrix — not just an excipient within the matrix” — must exhibit the appropriate characteristic. Id. at 1365 (emphasis omitted). We further explained that the matrix compositions are “limited by the *984 Markush groups” added during' prosecution “to overcome the examiner’s rejection of the claims as obvious.” Id. at 1367.

Summarizing the operation of the Mar-kush groups in the ’720 patent, we determined that “the correct construction requires that the inner volume contain substances from the group described for the inner lipophilic matrix (which are all lipophilic substances), and that the outer volume separately contain substances from the group described for the outer hydrophilic matrix (which are all hydro-philic).” Id.

On remand, the district court concluded that Watson’s ANDA Product satisfied the “inner lipophilic matrix” and “outer hydro-philic matrix” limitations. See 2016 Trial Decision, 2016 WL 1258885, at *4, *15. The court also determined that Watson’s ANDA Product satisfied the Markush limitations because the excipients falling outside the respective Markush groups were “unrelated” to the invention since they did not drive the water-affinity property of their respective matrices. Id. at *15. Watson appeals the district court’s constructions of “inner lipophilic matrix” and “outer hydrophilic matrix” and its findings of infringement. We have jurisdiction under 28 U.S.C. § 1295(a)(1).

II

“Following a bench trial, we review a district court’s conclusions of law de novo and its findings of fact for clear error.” Allergan, Inc. v. Sandoz Inc., 796 F.3d 1293, 1303 (Fed. Cir. 2015).

“A Markush claim is a particular kind of patent claim that lists alternative species or elements that can be selected as part of the claimed invention.” Multilayer Stretch Cling Film Holdings, Inc. v. Berry Plastics Corp., 831 F.3d 1350, 1357 (Fed. Cir. 2016). This typically appears in the form: “a member selected from the group consisting of A, B, and C.” 2015 Decision, 787 F.3d at 1363 n.3 (quoting Gillette Co. v. Energizer Holdings, Inc., 405 F.3d 1367, 1372 (Fed. Cir. 2005)).

Here, claim l’s (a) and (b) limitations use the phrase “consisting of,” or “consists of,” to characterize the matrix, and “consisting of’ to define the groups, which “creates a very strong presumption that that claim element is ‘closed’ and therefore ‘exclude[s] any elements, steps, or ingredients not specified in the claim.’ ” Multilayer Stretch Cling Film Holdings, 831 F.3d at 1358 (quoting AFG Indus., Inc. v. Cardinal IG Co.,

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848 F.3d 981, 121 U.S.P.Q. 2d (BNA) 1509, 2017 WL 541013, 2017 U.S. App. LEXIS 2393, Counsel Stack Legal Research, https://law.counselstack.com/opinion/shire-development-llc-v-watson-pharmaceuticals-inc-cafc-2017.