PAUL A. CROTTY, District Judge.
Plaintiffs Kowa Company, Ltd., Kowa Pharmaceuticals America, Inc., and Nissan Chemical Industries, Ltd. bring patent infringement claims against seven sets of Defendants.
Claim construction is a matter of law for the Court to decide. Markman v. Westview Instruments, Inc., 517 U.S. 370, 391 (1996). "Claim construction is a matter of resolution of disputed meanings and technical scope, to clarify and when necessary to explain what the patentee covered by the claims, for use in the determination of infringement." U.S. Surgical Corp. v. Ethicon, Inc., 103 F.3d 1554, 1568 (Fed. Cir. 1997). "When the parties raise an actual dispute regarding the proper scope of these claims, the court, not the jury, must resolve that dispute." O2 Micro Int'l Ltd. v. Beyond Innovation Tech. Co., 521 F.2d 1351, 1360 (Fed. Cir. 2008).
The `336 Patent consists of two claims. Claim 1 describes a chemical compound and Claim 2 states that the compound is used "for reducing hyperlipidemia, hyperlipoproteinemia or atherosclerosis." See Pl. Opening Brief ("Pl. Br."), Dkt. 65, Ex. 1 at col. 32, ll. 21-38. Defendants seek construction of Claim 1. As stated at the Markman hearing, "[a]ll the defendants want here in their construction is confirmation that all four stereoisomers are included, all mixtures of them are included, and that in no way shape, or form are any of them excluded." Transcript of Markman Hearing ("Tr.") at 11. There is no dispute because Plaintiffs agree that the claim covers all four stereoisomers of the compound depicted in Claim 1 and all mixtures thereof. See Tr. 6 ("[O]ne of ordinary skill in the art looking at that claim would clearly understand that ... there are four optical isomers which have the depicted structure. Claim 1 covers each of those."); Tr. 6 ("Where there are mixtures of stereoisomers, each of those stereoisomers in the mixture is covered by claim 1. Clearly such mixtures would also be covered within the scope of claim 1."); Tr. 7 ("The compound of formula 1 includes all the optical isomers and all the mixtures"); Tr. 7 ("Both parties agree that claim 1 as it's written and as it was allowed by the patent examiner calls the optical isomers and mixtures thereof"); Tr. 10 ("[C]ompound claims [such as this one] which don't include stereochemical terminology or symbols are interpreted as being without limitation as to stereochemical forms.").
Defendants' reliance on Infosint, S.A. v. H. Lundbeck A/S, 603 F.Supp.2d 748 (S.D.N.Y. 2009) in arguing for construction is unavailing. In that case, one party argued that the claim term in dispute covered only a single optical isomer, so construction was necessary to clarify that the claim covered all optical isomers. Id. at 756. Here, the parties agree that the claim covers all four optical isomers. Since Defendants have not "raise[d] an actual dispute regarding the proper scope of these claims", O2 Micro, 521 F.2d at 1360, claim construction is unnecessary.
The `477 Patent states that pitavastatin calcium (also known as NK-104), the active ingredient in Livalo, is "unstable at low pH, and many difficulties have been encountered in formulating it into preparations." See Pl. Br., Ex. 2 at col. 1, ll. 63-65. The patent describes a method to make a stable form of the compound in the pH range 6.8 to 7.8. Defendants seek construction of Claim 1, which reads in full:
Id. at col. 10, ll. 58-63. Defendants seek construction to clarify the method by which pH is measured. To answer this question, both Plaintiffs and Defendants point to the same explanatory language in the specification: The pH as referred to herein indicates the pH value to be determined in such a manner that a unit dose of a solid preparation comprising NK-104 or its salt or ester is sampled and dissolved or dispersed in from 1 to 10 ml of pure water, and the pH of the resulting aqueous solution or dispersion is measured.
Id. at 5. The parties agree that this language explains that pH is to be determined by taking a solid preparation of the pharmaceutical composition (likely a tablet), dissolving the tablet in 1 to 10 ml of pure water, and measuring the pH of the resulting solution. Compare Pl. Resp. Br., Dkt. 66 at 7 ("pH is to be measured by dissolving or dispersing a unit dose of the claimed pharmaceutical composition in from 1 to 10 ml of pure water"); and Tr. at 37 (Pl. Counsel: "[Y]ou take a unit dose of the — the thing you are trying to test is the pharmaceutical composition. You take a unit dose of that. You either disperse it or dissolve it in from 1 to 10 milliliters of pure water, and then you measure the pH of the resulting liquid."); with Def. Resp. Br., Dkt. 79 at 21 ("Defendants' proposed construction involves taking the `unit dose of a solid preparation of the pharmaceutical composition'; `dissolv[ing] or dispers[ing the unit dose] in 1 to 10 mL of pure water'; and then testing for pH"); and Tr. at 40-41 (Def. Counsel: "[Y]ou take a tablet, you're going to dissolve that tablet in 1 to 10 milliliters of pure water, and then a pH monitor is going to measure what the pH of that solution is.") Here too Defendants have not "raise[d] an actual dispute regarding the proper scope of these claims", O2 Micro, 521 F.2d at 1360; and claim construction is unnecessary.
The Court holds that claim construction is not necessary. The parties are directed to proceed with expert discovery according to the timeline as set forth in the Scheduling Order. See Dkt. 93.
SO ORDERED.