Glycobiosciences, Inc. v. Innocutis Holdings, LLC

146 F. Supp. 3d 221, 2015 U.S. Dist. LEXIS 159192, 2015 WL 7574749
District Court, District of Columbia·Decided November 25, 2015·No. Case Nos. 12-1901 15-592 (RDM)·Published·Cited by 1 cases

Opinion

MEMORANDUM OPINION REGARDING CLAIM CONSTRUCTION

RANDOLPH D. MOSS, United States District Judge

Plaintiff Glycobiosciences, Inc. filed this patent infringement .suit against Defendants Innocutis Holdings, LLC and Dara Biosciences, Inc., see Dkt. 1, alleging that Defendants indirectly or contributorily infringed U.S. Patent No. 6,387,407 (“the ’407 patent”) by importing, selling, or offering to sell Defendants’ BIONECT product, see Dkt. 23 ¶¶1 18, 25, 32, 38.1 Plaintiff subsequently filed a second infringement action asserting the ’407 patent against Defendant Fidia Farmacéutica, S.p.A (“Fidia”), the manufacturer of BIO-NECT. See No. 15-592, Dkt. 1. Given .the overlap in the complaints, the Court consolidated the cases. See June 10, 2015, Minute Order.

“A determination of [patent] infringement involves a two-step analysis. First, the claim must be properly construed to determine its scope and meaning. Second, the claim as properly construed must be compared to the accused device or process.” Omega Eng’g, Inc, v. Raytek Corp., 334 F.3d 1314, 1320 (Fed.Cir.2003) (internal quotation marks omitted). The matter before the Court pertains to the first step of this analysis: claim construction. See Dkts. 48, 49, 62, 63, 70, 72. The parties have asked the Court to construe two disputed terms in claim 1 of the ’407 patent: “nonionic polymer” and “weight average molecular weight'from about 650,000 to about 800,000.” See ’407 patent, col, 16:21-36 (emphases added).

For the reasons given below, and upon consideration of the ’407 patent, its prosecution history, the parties’ briefs and expert declarations, and the argument and testimony at the June 10, 2015, claim construction hearing, the Court concludes as follows: ■

(1) “Nonionic polymer” means a polymer composed of macromolecules that do not contain ionic bonds, ions, or functional groups that would ionize in aqueous solution under conditions applicable to the production of pharmaceutical5 products.

(2) The use of the word “about” in the phrase “[w]eight average molecular weight from about 650,000 to about 800,000” is not subject to a precise numerical definition. The meaning of the term, moreover, turns on both (a) consideration of fair notice to those skilled in the art regarding the scope of the claimed invention and (b) consideration of how variations in molecular weight affect the performance and characteristics of the claimed invention. Considering the [225]*225first factor, the Court concludes that the word “about” cannot admit of variations even approaching the ± 10% figure that Plaintiff attributes to the term. The Court accordingly recognizes a maximum possible variation in the claimed range.

The Court, however, reserves judgment as to whether the meaning of “about” can be affixed with greater precision based on the second factor. As explained below, the parties have yet to present the Court with sufficient evidence to permit it to assess how small variations in molecular weight might affect the functionality of ' the claimed invention. Thus, for present purposes, the Court merely concludes that- any variation in molecular weight even approaching ± 10% plainly falls beyond the scope of claim 1. In the face of uncertainty regarding the effect of small changes in molecular weight on the performance and characteristics of the invention, Defendants’ proposed range of variation of no more than ± 2% might have merit, while a somewhat wider range might be appropriate if Plaintiff can show that such; a variation would have no functional affect on thq invention.

I. BACKGROUND

The only patent presently asserted in this litigation is Plaintiffs ’407 patent, which issued on May 14, 2002.2 See Dkt. 23-1. That patent is directed to a topical— or “transdermal” — drug delivery process. See ’407 patent, col. 1:10-15. As explained in the patent’s specification, the claimed process involves the application of a water-based gel that may contain a therapeutic drug to the skin; the drug is released slowly over time as the gel penetrates .the tissues beneath the skin’s outer layer. See id. col. 1:10-15, col. 2:52-64; col. 3:29-46. The gel contains a blend of two polymer components: (1) “a negatively charged polymer material” called “hyaluronate sodium salt,” and (2) an unspecified “noniónic polymer.” Id. col. 16:26-31.

The ’407 patent’s . only independent claim, claim 1, recites:

wherein the negatively charged polymer material is hyaluronate sodium salt; and
wherein' the hyaluronate sodium salt has a weight average molecular weight from about 650,000 to about 800,000, a sulphated ash content below about 15%, a protein content below about 5%[,j and purity of at least 98%.

Id. col. 16:22-36 (emphases added). The parties ask the Court to resolve the meaning of two disputed claim terms: “nonionic polymer” and “weight average molecular weight from about 650,000 to about 800,-000.” Dkt. 61 at 1-2.

To set the stage for the parties’ dispute, it is necessary to review some basic chemistry. A; “polymer” is “[a] macromolecule formed by the chemical union of five or more identical combining units called [226]*226monomers.” Hawley’s Condensed Chemical Dictionary 1013 (15th ed. 2007) (“Haw-ley’s Dictionary”)', see also Dkt. 42-1 at 3 (Kolbert (I) Decl. ¶ ■ 10); Transcript of Claim Construction Hearing at 82-83 (“Markman Hearing”). The monomers are connected together in long, bead-like chains that are often made up of thousands of monomers. See Hawley’s Dictionary at 1013; see also Transcript of Technology Hearing (“Tech. Hearing”) at 24. The physical characteristics of a polymer are often dependent on the length of these chains. Dkt. 42-1 at 3 (Kolbert Decl. (I) ¶10).

Because the number of monomers in a polymer can vary, and this variation may affect the characteristics of the polymer, it can be important to specify its size, or “molecular weight.” Dkt. 63-7 at 2 (Ex. F).3 As with other polymers, “many of the biological functions of [hyaluronic acid] are dependent on molecular size,” Dkt. 63-8 at 2 (Ex. G),4 which explains why — as here— “the molecular weight of [hyaluronic acid] is a primary criterion in patents describing [hyaluronic acid] production,” Dkt. 63-7 at 2 (Ex. F at 2759). Generally speaking, changes in the molecular weight of hyalu-ronic acid affect its viscosity — its ability to flow. Markman Hearing at 67.

There are several ways to calculate molecular weight, see Dkt. 63-12 at 2-3 (Ex. K),5

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Glycobiosciences, Inc. v. Innocutis Holdings, LLC, 146 F. Supp. 3d 221, 2015 U.S. Dist. LEXIS 159192, 2015 WL 7574749 (D.D.C. 2015).

146 F. Supp. 3d 221 (Glycobiosciences, Inc. v. Innocutis Holdings, LLC) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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