The Regents of the University of California et al v. Affymetrix, Inc. et al

Filing 274

CLAIM CONSTRUCTION ORDER for '613 Patent, '303 Patent, '869 Patent, and '008 Patent. Claim Construction Hearing held no 8/31/2018. Court adopts the construction as set forth in this Order. Signed by Judge Marilyn L. Huff on 9/4/2018. (jah)

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1 2 3 4 5 6 7 8 UNITED STATES DISTRICT COURT 9 SOUTHERN DISTRICT OF CALIFORNIA 10 11 12 13 THE REGENTS OF THE UNIVERSITY OF CALIFORNIA; and BECTON, DICKINSON and COMPANY, Case No.: 17-cv-01394-H-NLS CLAIM CONSTRUCTION ORDER FOR THE ’613 PATENT, THE ’303 PATENT, THE ’869 PATENT, AND THE ’008 PATENT Plaintiffs, 14 15 v. 16 AFFYMETRIX, INC.; and LIFE TECHNOLOGIES CORP., 17 Defendants. 18 19 In the present action, Plaintiffs the Regents of the University of California, Becton, 20 Dickinson and Company, Sirigen, Inc., and Sirigen II Limited assert claims of patent 21 infringement against Defendants Affymetrix, Inc. and Life Technologies Corp., alleging 22 infringement of U.S. Patent No. 8,455,613, U.S. Patent No. 8,575,303, U.S. Patent No. 23 9,139,869, and U.S. Patent No. 9,547,008. 1 (Doc. No. 101, FAC ¶¶ 82-115.) On June 15, 24 25 26 27 28 1 In this action, Plaintiffs also assert claims of patent infringement against Defendants for infringement of U.S. Patent No. 9,085,799, U.S. Patent No. 8,110,673, and U.S. Patent No. 8,835,113 (Doc. No. 101, FAC ¶¶ 52-81.) The Court issued a prior claim construction order for the ’799 patent, the ’673 patent, and the ’113 patent on March 26, 2018. (Doc. No. 138.) In addition, on May 1, 2018, the Court granted Defendants’ motion for summary judgment of non-infringement of the ’799 patent. (Doc. No. 170.) 1 17-cv-01394-H-NLS 1 2018, the parties filed their joint claim construction prehearing statement, chart, and 2 worksheet, identifying the disputed claim terms from the ’613 patent, the ’303 patent, the 3 ’869 patent, and the ’008 patent. (Doc. No. 195.) On July 20, 2018, the parties each filed 4 an opening claim construction brief. (Doc. Nos. 219, 221.) On August 3, 2018, the parties 5 each filed a responsive claim construction brief. (Doc. No. 252, 253.) On August 30, 2018, 6 the Court issued a tentative claim construction order. (Doc. No. 270.) 7 The Court held a claim construction hearing on August 31, 2018. Donald R. Ware, 8 Barbara Fiacco, and Jesse Hindman appeared for Plaintiffs. Douglas E. Lumish, Jeffrey 9 G. Homrig, and Brent T. Watson appeared for Defendants. After considering the parties’ 10 briefs, the parties’ arguments at the hearing, and all relevant information, the Court 11 construes the disputed terms from the’613 patent, the ’303 patent, the ’869 patent, and the 12 ’008 patent. 13 Background 14 On July 10, 2017, Plaintiffs Regents and Becton, Dickinson filed a complaint for 15 patent infringement against Defendants Affymetrix and Life Technologies, alleging 16 infringement of U.S. Patent No. 9,085,799, U.S. Patent No. 8,110,673, and U.S. Patent No. 17 8,835,113. (Doc. No. 1, Compl.) On September 8, 2017, Defendants filed an answer to 18 Plaintiffs’ complaint. (Doc. No. 37.) 19 On October 6, 2017, the Court issued a scheduling order. (Doc. No. 55.) On 20 November 20, 2017, the Court denied Plaintiff Becton, Dickinson’s motion for a 21 preliminary injunction without prejudice. (Doc No. 69.) On November 30, 2017, the Court 22 issued an amended scheduling order. (Doc. No. 76.) 23 On February 7, 2018, the Court granted the parties’ joint motion for leave for 24 Plaintiffs to file a first amended complaint and to modify the scheduling order. (Doc. No. 25 100.) On February 9, 2018, Plaintiffs filed an amended complaint: (1) adding Sirigen and 26 Sirigen II as additional Plaintiffs and adding claims that Defendants’ products infringe four 27 Sirigen patents: U.S. Patent No. 9,547,008, U.S. Patent No. 9,139,869, U.S. Patent No. 28 8,575,303, and U.S. Patent No. 8,455,613; (2) adding infringement allegations against 2 17-cv-01394-H-NLS 1 additional accused products; and (3) adding allegations of induced infringement against 2 Defendants. (Doc. No. 101, FAC.) 3 On February 23, 2018, the Court issued a second amended scheduling order. (Doc. 4 No. 105.) On March 26, 2018, the Court issued a claim construction order, construing 5 disputed claim terms from the ’799 patent, the ’673 patent, and the ’113 patent. (Doc. No. 6 138.) On May 1, 2018, the Court granted Defendants’ motion for summary judgment of 7 non-infringement of the ’799 patent. (Doc. No. 170.) On May 14, 2018, the Court denied 8 Defendants’ motion for summary judgment of non-infringement of the ’673 patent and the 9 ’113 patent. (Doc. No. 183.) 10 By the present claim construction briefs, the parties request that the Court construe 11 disputed claim terms from the’613 patent, the ’303 patent, the ’869 patent, and the ’008 12 patent. (Doc. Nos. 219, 221.) The’613 patent, the ’303 patent, the ’869 patent, and the 13 ’008 patent are all entitled “Reagents for Directed Biomarker Signal Amplification,” and 14 these patents all share a common specification. U.S. Patent No. 8,455,613 (filed Jun. 4, 15 2013), at (54); U.S. Patent No. 8,575,303 (filed Nov. 5, 2013), at (54); U.S. Patent No. 16 9,139,869 (filed Sep. 22, 2015), at (54); U.S. Patent No. 9,547,008 (filed Jan. 17, 2017), at 17 (54). The invention disclosed in the patents at issue relate to “neutral conjugated water- 18 soluble polymers with linkers along the polymer main chain structure and terminal end 19 capping units.” ’613 Patent at (57) (abstract). 20 As an exemplary claim, Claim 1 of the ’303 Patent provides: 21 1. A water soluble conjugated polymer having the structure of Formula (Ia): 22 23 24 25 26 27 28 3 17-cv-01394-H-NLS 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 wherein: each R is independently a non-ionic side group capable of imparting solubility in water in excess of 10 mg/mL; MU is a polymer modifying unit or band gap modifying unit that is evenly or randomly distributed along the polymer main chain and is optionally substituted with one or more optionally substituted substituents selected from halogen, hydroxyl, C1-C12 alkyl, C2-C12 alkene, C2-C12 alkyne, C3-C12 cycloalkyl, C1-C12 haloalkyl, C1-C12 alkoxy, C2-C18 (hetero)aryloxy, C2-C18 (hetero)arylamino, (CH2)x′(OCH2CH2)y′OCH3 where each x′ is independently an integer from 0-20, y′ is independently an integer from 0 to 50, or a C2-C18 (hetero)aryl group; each optional linker L1 and L2 are aryl or heteroaryl groups evenly or randomly distributed along the polymer main chain and are substituted with one or more pendant chains terminated with a functional group selected from amine, carbamate, carboxylic acid, carboxylate, maleimide, activated esters, N-hydroxysuccinimidyl, hydrazines, hydrazids, hydrazones, azide, alkyne, aldehydes, thiols, and protected groups thereof for conjugation to another substrate, molecule or biomolecule; G1 and G2 are each independently selected from hydrogen, halogen, alkyne, optionally substituted aryl, optionally substituted heteroaryl, halogen substituted aryl, boronic acid substituted aryl, boronic ester substituted aryl, boronic esters, boronic acids, optionally substituted fluorine and aryl or heteroaryl substituted with one or more pendant chains terminated with a functional group, molecule or biomolecule selected from amine, carbamate, carboxylic acid, carboxylate, maleimide, activated esters, Nhydroxysuccinimidyl, hydrazines, hydrazids, hydrazones, azide, alkyne, 4 17-cv-01394-H-NLS 1 aldehydes, thiols, and protected groups thereof for conjugation to another substrate, molecule or biomolecule; 2 3 wherein the polymer comprises at least 1 functional group selected from amine, carbamate, carboxylic acid, carboxylate, maleimide, activated esters, N-hydroxysuccinimidyl, hydrazines, hydrazids, hydrazones, azide, alkyne, aldehydes, and thiols within G1, G2, L1 or L2 that allows, for functional conjugation to another molecule, substrate or biomolecule; 4 5 6 7 n is an integer from 1 to about 10,000; and 8 a, b, c and d define the mol % of each unit within the structure which each can be evenly or randomly repeated and where a is a mol % from 10 to 100%, b is a mol % from 0 to 90%, and each c and d are mol % from 0 to 25%. 9 10 11 ’303 Patent at 239:29-240:56. 12 13 Discussion I. Legal Standards for Claim Construction 14 Claim construction is an issue of law for the court to decide. Teva Pharm. USA, Inc. 15 v. Sandoz, Inc., 135 S. Ct. 831, 838 (2015); Markman v. Westview Instr., Inc., 517 U.S. 16 370, 372 (1996). Although claim construction is ultimately a question of law, “subsidiary 17 factfinding is sometimes necessary.” Teva, 135 S. Ct. at 838. 18 “The purpose of claim construction is to ‘determin[e] the meaning and scope of the 19 patent claims asserted to be infringed.’” O2 Micro Int’l Ltd. v. Beyond Innovation Tech. 20 Co., 521 F.3d 1351, 1360 (Fed. Cir. 2008). “It is a ‘bedrock principle’ of patent law that 21 the ‘claims of a patent define the invention to which the patentee is entitled the right to 22 exclude.’” Phillips v. AWH Corp., 415 F.3d 1303, 1312 (Fed. Cir. 2005) (en banc). 23 Claim terms “‘are generally given their ordinary and customary meaning[,]’” which 24 “is the meaning that the term would have to a person of ordinary skill in the art in question 25 at the time of the invention.” Id. at 1312–13. “In some cases, the ordinary meaning of 26 claim language as understood by a [PHOSITA] may be readily apparent even to lay judges, 27 and claim construction in such cases involves little more than the application of the widely 28 accepted meaning of commonly understood words.” Id. at 1314. “However, in many 5 17-cv-01394-H-NLS 1 cases, the meaning of a claim term as understood by persons of skill in the art is not readily 2 apparent.” O2 Micro, 521 F.3d at 1360. If the meaning of the term is not readily apparent, 3 the court must look to “those sources available to the public that show what a person of 4 skill in the art would have understood disputed claim language to mean,” including intrinsic 5 and extrinsic evidence. See Phillips, 415 F.3d at 1314. A court should begin with the 6 intrinsic record, which consists of the language of the claims, the patent specification, and, 7 if in evidence, the prosecution history of the asserted patent. Id.; see also Vederi, LLC v. 8 Google, Inc., 744 F.3d 1376, 1382 (Fed. Cir. 2014) (“In construing claims, this court relies 9 primarily on the claim language, the specification, and the prosecution history.”). 10 In determining the proper construction of a claim, a court should first look to the 11 language of the claims. See Vitronics, 90 F.3d at 1582; see also Comark Commc’ns v. 12 Harris Corp., 156 F.3d 1182, 1186 (Fed. Cir. 1998) (“The appropriate starting point . . . is 13 always with the language of the asserted claim itself.”). The context in which a disputed 14 term is used in the asserted claims may provide substantial guidance as to the meaning of 15 the term. See Phillips, 415 F.3d at 1314. In addition, the context in which the disputed 16 term is used in other claims, both asserted and unasserted, may provide guidance because 17 “the usage of a term in one claim can often illuminate the meaning of the same term in 18 other claims.” Id. Furthermore, a disputed term should be construed “consistently with its 19 appearance in other places in the same claim or in other claims of the same patent.” 20 Rexnord Corp. v. Laitram Corp., 274 F.3d 1336, 1342 (Fed. Cir. 2001); accord 21 Microprocessor Enhancement Corp. v. Texas Instruments Inc., 520 F.3d 1367, 1375 (Fed. 22 Cir. 2008); see also Paragon Sols., LLC v. Timex Corp., 566 F.3d 1075, 1087 (Fed. Cir. 23 2009) (“We apply a presumption that the same terms appearing in different portions of the 24 claims should be given the same meaning.” (internal quotation marks omitted)). Moreover, 25 “‘[a] claim construction that gives meaning to all the terms of the claim is preferred over 26 one that does not do so.’” Vederi, 744 F.3d 1383. 27 A court must also read claims “in view of the specification, of which they are a part.” 28 Markman, 52 F.3d at 979; see 35 U.S.C. § 112(b) (“The specification shall conclude with 6 17-cv-01394-H-NLS 1 one or more claims particularly pointing out and distinctly claiming the subject matter 2 which the inventor or a joint inventor regards as the invention.”). “‘Apart from the claim 3 language itself, the specification is the single best guide to the meaning of a claim term.’” 4 Vederi, 744 F.3d at 1382. For example, “a claim construction that excludes [a] preferred 5 embodiment [described in the specification] ‘is rarely, if ever, correct and would require 6 highly persuasive evidentiary support.’” Adams Respiratory Therapeutics, Inc. v. Perrigo 7 Co., 616 F.3d 1283, 1290 (Fed. Cir. 2010). 8 But “[t]he written description part of the specification does not delimit the right to 9 exclude. That is the function and purpose of claims.” Markman v. Westview Instruments, 10 Inc., 52 F.3d 967, 980 (Fed. Cir. 1995) (en banc). Therefore, “it is improper to read 11 limitations from a preferred embodiment described in the specification—even if it is the 12 only embodiment—into the claims absent a clear indication in the intrinsic record that the 13 patentee intended the claims to be so limited.” Dealertrack, Inc. v. Huber, 674 F.3d 1315, 14 1327 (Fed. Cir. 2012); see also Kara Tech. Inc. v. Stamps.com Inc., 582 F.3d 1341, 1348 15 (Fed. Cir. 2009) (“The patentee is entitled to the full scope of his claims, and we will not 16 limit him to his preferred embodiment or import a limitation from the specification into the 17 claims.”). 18 In most situations, analysis of the intrinsic evidence will resolve claim construction 19 disputes. See Vitronics, 90 F.3d at 1583; Teva, 135 S. Ct. at 841. However, “[w]here the 20 intrinsic record is ambiguous, and when necessary,” district courts may “rely on extrinsic 21 evidence, which ‘consists of all evidence external to the patent and prosecution history, 22 including expert and inventor testimony, dictionaries, and learned treatises.’” Power 23 Integrations, Inc. v. Fairchild Semiconductor Int’l, Inc., 711 F.3d 1348, 1360 (Fed. Cir. 24 2013) (quoting Phillips, 415 F.3d at 1317). A court must evaluate all extrinsic evidence in 25 light of the intrinsic evidence. Phillips, 415 F.3d at 1319. “Extrinsic evidence may not be 26 used ‘to contradict claim meaning that is unambiguous in light of the intrinsic evidence.’” 27 Summit 6, LLC v. Samsung Elecs. Co., 802 F.3d 1283, 1290 (Fed. Cir. 2015); see also Bell 28 Atl. Network Servs., Inc. v. Covad Commc’ns Grp., Inc., 262 F.3d 1258, 1269 (Fed. Cir. 7 17-cv-01394-H-NLS 1 2001) (“[E]xtrinsic evidence . . . may not be used to vary, contradict, expand, or limit the 2 claim language from how it is defined, even by implication, in the specification or file 3 history.”); Vederi, 744 F.3d at 1382 (“[E]xtrinsic evidence may be less reliable than the 4 intrinsic evidence.”). In cases where subsidiary facts contained in the extrinsic evidence 5 “are in dispute, courts will need to make subsidiary factual findings about that extrinsic 6 evidence.” Teva, 135 S. Ct. at 841. 7 “[D]istrict courts are not (and should not be) required to construe every limitation 8 present in a patent’s asserted claims.” O2 Micro, 521 F.3d at 1362. In certain situations, 9 it is appropriate for a court to determine that a claim term needs no construction and its 10 plain and ordinary meaning applies. See id.; Phillips, 415 F.3d at 1314. But “[a] 11 determination that a claim term ‘needs no construction’ or has the ‘plain and ordinary 12 meaning’ may be inadequate when a term has more than one ‘ordinary’ meaning or when 13 reliance on a term’s ‘ordinary’ meaning does not resolve the parties’ dispute.” O2 Micro, 14 521 F.3d at 1361. If the parties dispute the scope of a certain claim term, it is the court’s 15 duty to resolve the dispute. Id. at 1362; accord Eon Corp. IP Holdings v. Silver Spring 16 Networks, 815 F.3d 1314, 1318 (Fed. Cir. 2016). 17 II. Analysis of the Disputed Claim Terms 18 A. 19 Plaintiffs propose that the term “NH2” be construed as “an -NH2 group, or an -NH- 20 group that is the product of conjugation of an -NH2 group to another chemical group.” 21 (Doc. No. 221 at 6.) In their briefing, Defendants propose that the term “NH2” be construed 22 as “an -NH2 group.” (Doc. No. 219 at 7.) Following the issuance of the Court’s tentative 23 claim construction, at the claim construction hearing, Defendants submitted a revised claim 24 construction for the term “NH2” proposing that the term be construed as “an -NH2 group, 25 which may be used in a reaction that results in an -NH group conjugated to another 26 chemical group.” Because the parties dispute the scope of this claim term, the Court must 27 resolve the parties’ dispute. See O2 Micro, 521 F.3d at 1361; Eon, 815 F.3d at 1318. 28 “NH2” As an initial matter and in an effort to provide context to the present claim 8 17-cv-01394-H-NLS 1 construction dispute, the Court notes that both parties’ experts agree that after a -NH2 group 2 is conjugated to another group, the chemical structure is no longer -NH2. (Doc. No. 195- 3 3, Swager Decl. ¶¶ 10, 13; Doc. No. 195-4, Burgess Decl. ¶ 33.) The end product is 4 -NH-, not -NH2. (Id.) 5 The Court now turns to the claim language at issue. Claim 1 of the ’303 Patent 6 claims “[a] water soluble conjugated polymer” having a structure where “each optional 7 linker L1 and L2 are . . . for conjugation to another substrate, molecule or biomolecule.” 8 ’303 Patent at 239:58-67. Further, dependent claim 5 of the ’303 patent expressly claims 9 the polymer of claim 1 “wherein optional linker L1 or L2 are” a structure including “NH2.” 10 Id. at 244:36-50; see also ’613 Patent at 231:2, 232:20-38. Here, claim 5 of the ’303 patent 11 describes a polymer having a linker with a -NH2 group that allows the polymer to be 12 conjugated to another substrate, molecule, or biomolecule. See Phillips, 415 F.3d at 1314 13 (“[T]he usage of a term in one claim can often illuminate the meaning of the same term in 14 other claims.”). And the parties’ experts agree that once a -NH2 group is conjugated to 15 another group, the chemical structure is -NH-, not -NH2. (Doc. No. 195-3, Swager Decl. 16 ¶¶ 10, 13; Doc. No. 195-4, Burgess Decl. ¶ 33.) Thus, Defendant’s initial proposed 17 construction construing the term “NH2” as simply “an -NH2 group” would be improper 18 because it fails to acknowledge that once a -NH2 group is conjugated to another group, 19 something that is expressly contemplated by the claim language, the chemical structure 20 becomes -NH-, not -NH2. 21 As revised, both parties’ claim construction now properly reflects the fact that once 22 a -NH2 group is conjugated to another group, the chemical structure becomes -NH-. 23 Defendants argue that their revised proposed construction is preferable over Plaintiffs’ 24 proposal, because their construction properly reflects that when the claims at issue refer to 25 “NH2,” it is at the pre-conjugation stage. The Court agrees. For example, dependent claim 26 5 of the ’303 patent claims linkers with a structure including a “NH2” group. ’303 Patent 27 at 244:36-50. Claim 1, from which claim 5 depends, explains that the linkers are “for 28 conjugation to another substrate, molecule or biomolecule.” Id. at 239:66-67. Thus, under 9 17-cv-01394-H-NLS 1 the plain language of the claims, the claims are describing the linkers at the pre-conjugation 2 stage. The claims describe the linkers as components of the polymer that are then used 3 “for conjugation” to another group. 4 Further, in describing the linkers, the claims distinguish -NH- from -NH2. For 5 example, dependent claim 4 of ’303 patent claims a polymer “wherein optional linkers L1 6 or L2 are selected from the group consisting of a-j having the structures: 7 8 9 10 11 12 13 14 15 16 ’303 Patent at 240:66-241:10; see also ’613 Patent at 231:60-65. The fact that the claims 17 are careful to distinguish -NH- from -NH2 in claiming the structures at issue further 18 supports the notion that the claims when describing these structures are describing them at 19 the pre-conjugation stage. Defendants’ revised proposed claim construction reflects this 20 concept whereas Plaintiffs’ proposed construction does not. As a result, Defendants’ 21 revised proposed construction is preferable over Plaintiffs’ proposal. 22 In addition, Defendants’ revised proposed construction is supported by the patents’ 23 common specification. 24 chromophore is attached to the polymer via the NH2 group.” ’613 Patent at 21:1-2. Here, 25 the specification describes using a NH2 group to attach a signaling chromophore to the 26 polymer. In this passage, as in the claims, the specification describes the NH2 group as 27 being at the pre-conjugation stage. As such, the specification also supports Defendants’ 28 revised proposed construction. The specification provides: “In some instances, a signaling 10 17-cv-01394-H-NLS 1 In sum, the Court adopts Defendants’ revised proposed construction for this claim 2 term, and the Court rejects Plaintiffs’ proposed construction. The Court construes the term 3 “NH2” as “an -NH2 group, which may be used in a reaction that results in an -NH group 4 conjugated to another chemical group.” 5 B. 6 Plaintiffs propose that the term “polymer modifying unit” be construed as “a unit in 7 the polymer different than the units wherein the ratios are denoted by the letters a, c, and 8 d.” (Doc. No. 221 at 12.) Defendants argue that the claim term “polymer modifying unit” 9 is indefinite. (Doc. No. 219 at 11.) “polymer modifying unit” 10 Section 112 of the Patent Act requires that a patent’s specification “conclude with 11 one or more claims particularly pointing out and distinctly claiming the subject matter 12 which the applicant regards as [the] invention.” 35 U.S.C. § 112, ¶ 2. In Nautilus, Inc. v. 13 Biosig Instruments, Inc., 134 S. Ct. 2120, 2124 (2014), the Supreme Court “h[e]ld that a 14 patent is invalid for indefiniteness if its claims, read in light of the specification delineating 15 the patent, and the prosecution history, fail to inform, with reasonable certainty, those 16 skilled in the art about the scope of the invention.” See also id. at 2129 (“[W]e read § 112, 17 ¶ 2 to require that a patent’s claims, viewed in light of the specification and prosecution 18 history, inform those skilled in the art about the scope of the invention with reasonable 19 certainty.”). Definiteness is measured from the viewpoint of a PHOSITA at the time the 20 patent was filed. Id. at 2128. 21 Indefiniteness is a question of law involving underlying factual determinations. 22 Teva Pharm. USA, Inc. v. Sandoz, Inc., 789 F.3d 1335, 1341 (Fed. Cir. 2015); Green Edge 23 Enters., LLC v. Rubber Mulch Etc., LLC, 620 F.3d 1287, 1299 (Fed. Cir. 2010). The party 24 challenging the validity of the patents-in-suit bears the burden of proving indefiniteness by 25 clear and convincing evidence. See Nautilus, 134 S. Ct. at 2130 n.10 (citing Microsoft 26 Corp. v. i4i Ltd. Partnership, 131 S. Ct. 2238, 2242 (2011)); see, e.g., Teva, 789 F.3d at 27 1345. 28 11 17-cv-01394-H-NLS 1 Defendants argue that the term “polymer modifying unit” is indefinite because the 2 term has no meaning to a person of ordinary skill in the art, and the common specification 3 for the patent provides no guidance as to its meaning. (Doc. No. 219 at 11.) Defendants 4 state that the term “polymer modifying unit” is not a term of art, and it has no commonly 5 accepted definition. (Id. at 13.) But even assuming this is true, there is no requirement 6 that a claim term must be a term of art or have a commonly accepted definition in order to 7 be definite under section 112. 8 Defendants further argue that the common specification for the patents fails to 9 provide sufficient guidance to a person of skill in the art as to the meaning of the term. 10 (Doc. No. 219 at 13.) The Court disagrees. The term itself provides guidance as to its 11 meaning. The Court agrees with Plaintiffs that each of the words used in the phrase 12 “polymer modifying unit” has a common meaning that is understandable to a person of 13 ordinary skill in the art. (Doc. No. 221 at 12.) Under its plain language, the term means a 14 unit in the claimed polymer that modifies the polymer. Further, the specification provides 15 sufficient examples of how the claimed polymer can be modified, giving one skilled in the 16 art reasonable certainty regarding the scope of the claim term. See ’613 Patent at 52:1-19. 17 As a result, Defendants have failed to meet their burden of establishing that the claim term 18 “polymer modifying unit” is indefinite. 19 Plaintiffs’ proposed construction is supported by the claim language. For example, 20 claim 1 of the ’303 patent claims “[a] water soluble conjugated polymer having the 21 structure of Formula (Ia): 22 23 24 25 26 27 28 12 17-cv-01394-H-NLS 1 2 3 4 5 6 7 8 9 wherein: . . . MU is a polymer modifying unit . . . . ’303 Patent at 239:29-46. Here, the 10 claim depicts the polymer modifying unit as being a unit that is different from the units that 11 are denoted by the letter a, c, and d. Nevertheless, the Court slightly alters Plaintiffs’ 12 proposed construction to include the requirement that the unit modify the polymer. 13 In sum, the Court rejects Defendants’ contention that the claim term “polymer 14 modifying unit” is indefinite. The Court adopts Plaintiffs’ proposed constructed as 15 modified. The Court construes “polymer modifying unit” as “a unit in the polymer that 16 modifies the polymer and is different than the units wherein the ratios are denoted by the 17 letters a, c, and d.” 18 C. “band gap modifying unit” 19 Plaintiffs propose that the term “band gap modifying unit” be construed as “a unit in 20 the polymer that modifies the wavelengths at which the polymer absorbs or emits light.” 21 (Doc. No. 221 at 14.) Defendants propose that the term be construed as “a unit in the 22 polymer that either increases or decreases the band gap of the polymer.” (Doc. No. 219 at 23 17.) Because the parties dispute the scope of this claim term, the Court must resolve the 24 parties’ dispute. See O2 Micro, 521 F.3d at 1361; Eon, 815 F.3d at 1318. 25 As an initial matter, the Court notes that the parties and their experts agree on the 26 definition for the term “band gap.” Plaintiffs’ expert, Dr. Swager, explains that: “A ‘band 27 gap’ is a particular property of a material that refers to the energy gap between the highest 28 occupied molecular orbital and the lowest unoccupied molecular orbital.” (Doc. No. 19513 17-cv-01394-H-NLS 1 3, Swager Decl. ¶ 31.) Defendants’ expert, Dr. Burgess, explains: “The term ‘band gap’ is 2 conceptually used to describe the gap in energy between the highest occupied molecular 3 orbital and the lowest unoccupied molecular orbital.” (Doc. No. 195-4, Burgess Decl. ¶ 4 43.) In light of this agreement between the experts as to the term “band gap,” the Court 5 construes the term “band gap” as “the energy gap between the highest occupied molecular 6 orbital and the lowest unoccupied molecular orbital.” 7 Turning to the full phrase “band gap modifying unit,” Defendants’ proposed 8 construction is supported by a review of the intrinsic record. The claim language provides 9 an initial definition for this claim term. For example, claim 1 of the ’303 patent claims: “A 10 water soluble conjugated polymer having the structure of Formula (Ia) . . . wherein: . . . 11 MU is a polymer modifying unit or band gap modifying unit that is evenly or randomly 12 distributed along the polymer main chain.” ’303 Patent at 239:29-48. Here, the plain 13 language of claim 1 of the ’303 patent describes the “band gap modifying unit” as a unit in 14 the polymer that modifies the band gap. Further, the specification explains the manner in 15 which these units modify the bandgap. 16 “Incorporation of repeat units that decrease the band gap can produce conjugated polymers 17 with such characteristics.” ’613 Patent at 52:41-42. Here, the specification explains that 18 the units at issue modify the band gap by decreasing it. As such, Defendants’ proposed 19 construction providing that a “band gap modifying unit” is a unit in the polymer that either 20 increases or decreases the band gap is well supported by the intrinsic record. 2 The common specification provides: 21 Plaintiffs argue that Defendants’ proposed construction for the term “band gap 22 modifying unit” would be unhelpful to the jury because it uses the technical term “band 23 gap” within the proposed construction. (Doc. No. 221 at 15.) But any concerns regarding 24 Defendants’ use of the term “band gap” in their proposed construction are alleviated by the 25 26 27 28 2 In their claim construction brief, Defendants argue that the Court’s construction for the term “band gap modifying unit” should cover both increasing and decreasing the band gap. (Doc. No. 219 at 18-20.) In response, Plaintiffs explain that it is not their position that that the “band gap modifying unit” should be read narrowly to mean only decreasing the band gap. (Doc. No. 252 at 8.) As such, the Court’s construction for this claim term will cover both increasing and decreasing the band gap. 14 17-cv-01394-H-NLS 1 Court separately construing the term “band gap” based on the experts’ agreed upon 2 definition. As such, the Court rejects Plaintiffs’ contention. In addition, the Court agrees 3 with Defendants that Plaintiffs’ proposed construction is flawed because it replaces the 4 agreed meaning of the term “band gap” with its downstream effect. (See Doc. No. 219 at 5 18.) 6 In sum, the Court adopts Defendants’ proposed construction for this claim term, and 7 the Court rejects Plaintiffs’ proposed construction. The Court construes the term “band 8 gap modifying unit” as “a unit in the polymer that either increases or decreases the band 9 gap of the polymer.” 10 D. 11 Plaintiffs propose that the term “solubility” be construed as “miscible in a solvent 12 with no visible particulates.” (Doc. No. 221 at 16.) Defendants propose that the term 13 “solubility” be construed as “ability or tendency of a substance to dissolve a solvent.” 14 (Doc. No. 219 at 20.) Here, the parties dispute whether the term “solubility” requires that 15 the polymer be capable of being mixed in water or an aqueous solution such that no visible 16 particulates remain. Because the parties dispute the scope of this claim term, the Court 17 must resolve the parties’ dispute. See O2 Micro, 521 F.3d at 1361; Eon, 815 F.3d at 1318. 18 In support of their proposed claim construction, Plaintiffs argue that the common 19 specification for the patents at issue provides an express definition for the term “solubility.” 20 (Doc. No. 221 at 16.) The Court agrees. The common specification provides: “Non-ionic 21 side groups capable of imparting solubility in water as used herein refer to side groups 22 which are not charged and allow the resulting polymer to be soluble in water or aqueous 23 solutions with no visible particulates.” ’613 Patent at 54:8-11. Here, the common 24 specification explains that the term “imparting solubility” with respect to non-ionic side 25 groups “as used herein” means to allow “the resulting polymer to be soluble in water or 26 aqueous solutions with no visible particulates.” Id. Plaintiffs’ proposed construction 27 properly incorporates this definition from the common specification. See Honeywell Int’l, 28 Inc. v. Universal Avionics Sys. Corp., 493 F.3d 1358, 1361 (Fed. Cir. 2007) (“When a “solubility” 15 17-cv-01394-H-NLS 1 patentee defines a claim term, the patentee’s definition governs, even if it is contrary to the 2 conventional meaning of the term. A claim term may be defined in a particular manner for 3 purposes of a patent even ‘without an explicit statement of redefinition.’” (citation 4 omitted)); Phillips, 415 F.3d at 1321 (“[T]he specification ‘acts as a dictionary when it 5 expressly defines terms used in the claims or when it defines terms by implication.’”). 6 Defendants argue that the passage at issue does not set forth a clear definition for the 7 term “solubility.” (Doc. No. 253 at 9.) Defendants note that the common specification for 8 the patents at issue contains a specific section entitled “definitions,” but the passage 9 Plaintiffs rely on from the specification is not in that section, and the “definitions” section 10 does not include a definition for the term “solubility.” (Id. at (citing ’613 Patent at 37:63- 11 41:55).) But the fact that the passage at issue is not included in the “definitions” section 12 of the specification is of no consequence. In the passage at issue, the specification uses 13 clear definitional language when it uses the phrase “as used herein refer to” when 14 describing the non-iconic side groups capable of imparting solubility in water. ’613 Patent 15 at 54:8-11. In light of this language, this passage in the specification sets forth a definition 16 even if it is not specifically found within the “definitions” section of the specification. 17 Defendants also argue that the passage at issue fails to set forth a clear definition for 18 the specific term “solubility” because the passage is merely describe a preferred 19 embodiment of the claimed invention, the “non-ionic side groups” embodiment. (Doc. No. 20 219 at 21.) The Court recognizes that “it is improper to read limitations from a preferred 21 embodiment described in the specification—even if it is the only embodiment—into the 22 claims absent a clear indication in the intrinsic record that the patentee intended the claims 23 to be so limited.” Dealertrack, 674 F.3d at 1327. In addition, the Court recognizes that the 24 invention at issue is not limited to “non-ionic side groups.” But Defendants’ argument fails 25 to appreciate the context in which the term “solubility” is used in the asserted claims. For 26 example, claim 1 of the ’303 patent claims “[a] water soluble conjugated polymer” wherein 27 “each R is independently a non-ionic side group capable of imparting solubility in water in 28 excess of 10 mg/mL.” ’303 Patent at 239:43-44; see also id. at 254:39-40 (claim 27), 16 17-cv-01394-H-NLS 1 262:55-56 (claim 33). Claim 4 of the ’008 patent uses similar language in claiming: 2 “wherein each R is a non-ionic side group capable of imparting solubility in water in excess 3 of 10 mg/mL.” ’008 Patent at 226:21-22; see also id. at 229:44-45 (claim 9). Here, the 4 claim 1 of the ’303 patent and claim 4 of the ’008 patent use the term “solubility” in the 5 context of describing “non-ionic side groups,” which is the exact same context as that term 6 is used in the passage at issue from the specification. Thus, the definition from the 7 specification controls in this context. As such, the Court rejects Defendants arguments.3 8 Defendants further argue that Plaintiffs’ proposed construction is flawed because it 9 uses the term “miscible,” which refers to the ability of liquids and gasses to mix. (Doc. 10 No. 219 at 21-22.) Defendants argue that conjugated polymers are neither liquid nor gas, 11 and, thus, the word “miscible” makes no sense in this context. (Id. at 22.) In response, 12 Plaintiff explain that the words “mixable” and “miscible” are synonyms. (Doc. No. 252 at 13 9 n.3.) As such, the Court slightly alters Plaintiffs’ proposed construction for this term to 14 use the word “mixable” instead of “miscible.” 4 15 In support of their proposed construction, Defendants merely rely on extrinsic 16 evidence, specifically expert testimony and dictionary definitions. (Doc. No. 219 at 20.) 17 But “[e]xtrinsic evidence may not be used ‘to contradict claim meaning that is 18 unambiguous in light of the intrinsic evidence.’” Summit 6, 802 F.3d at 1290; see Bell Atl. 19 Network, 262 F.3d at 1269. The common specification contains clear language explaining 20 what is meant by the term “solubility.” Accordingly, Defendants cannot use extrinsic 21 evidence to contradict or vary this clear language contained in the specification. 22 In sum, the Court adopts Plaintiffs’ proposed construction for this claim term, and 23 24 25 26 27 28 3 The Court recognizes that the ’008 patent and the ’869 patent have claims that more broadly claim “a side group capable of imparting solubility in water.” See, e.g., ’869 Patent at 235:24-25; ’008 Patent at 225:22-23. But even in these claims, the claims use the term “solubility” in the context of describing “a side group,” which is a similar context to how the term “solubility” is used in the specification passage at issue. 4 At the hearing, Plaintiffs stated that they did not object to the Court replacing the word “miscible” with “mixable” in its construction for this claim term. 17 17-cv-01394-H-NLS 1 the Court rejects Defendants’ proposed construction. The Court construes the term 2 “solubility” as “mixable in a solvent with no visible particulates.” 3 4 E. “where the specific signal is at least 3 fold greater than the same antibody conjugated to Pacific Blue” 5 Plaintiffs argue that the claim term “where the specific signal is at least 3 fold greater 6 than the same antibody conjugated to Pacific Blue” needs no construction. (Doc. No. 221 7 at 16.) Plaintiffs propose, in the alternative, that if this claim term must be construed, the 8 Court construe the claim term as “a specific signal that is at least 3 fold greater than the 9 signal of the same antibody conjugated to the fluorescent dye Pacific Blue, with an inherent 10 upper limit in the range of about 20-25 fold.” (Doc. No. at 17.) Defendants propose that 11 this claim term be construed as “a specific signal that is 3 fold or more greater than the 12 signal of the same antibody conjugated to Pacific Blue, with no upper limit.” (Doc. No. 13 219 at 22.) Here, the parties dispute whether the phrase “at least three fold greater” contains 14 an inherent upper limit of about 20-25 fold. Because the parties dispute the scope of this 15 claim term, the Court must resolve the parties’ dispute. See O2 Micro, 521 F.3d at 1361; 16 Eon, 815 F.3d at 1318. 17 The Court begins its analysis of the parties’ dispute regarding the phrase “at least 3 18 fold greater” by examining the claim language. The claim language places no express 19 upper limit on the increase in signal. For example, claim 21 of the ’303 patent provides: 20 “The water soluble conjugated polymer of claim 20, wherein the polymer and antibody 21 excited at about 405 nm in a flow cytometry assay where the specific signal is at least 3 22 fold greater than the same antibody conjugated to Pacific Blue.” ’303 Patent at 253:66- 23 254:3. The claim language of claim 1 of the ’799 patent requires that the signal generated 24 by the polymer and the antibody be at least 3 fold greater than when the same antibody is 25 conjugated to Pacific Blue. The claim language does not provide an upper range. The 26 claim language merely requires that the increase be at least 3 fold greater. Further, the 27 Court notes that the Federal Circuit has held that “‘[o]pen-ended claims are not inherently 28 improper.’” Andersen Corp. v. Fiber Composites, LLC, 474 F.3d 1361, 1376 (Fed. Cir. 18 17-cv-01394-H-NLS 1 2007) (quoting Scripps Clinic & Research Found. v. Genentech, Inc., 927 F.2d 1565, 1572 2 (Fed. Cir. 1991)). 3 construction, not Plaintiffs’ proposal. Accordingly, the claim language supports Defendants’ proposed 4 In support of their assertion that the phrase “at least 3 fold greater” has an inherent 5 upper limit of about 20-25 fold, Plaintiffs rely on Federal Circuit case law holding that 6 open-ended claims have inherent upper limits. (Doc. No. 221 at 17.) In Andersen Corp. 7 v. Fiber Composites, LLC, the Federal Circuit explained that open-ended claims are 8 permissible, and “‘they may be supported if there is an inherent, albeit not precisely known, 9 upper limit and the specification enables one of skill in the art to approach that limit.’” 10 Andersen Corp. v. Fiber Composites, LLC, 474 F.3d 1361, 1376–77 (Fed. Cir. 2007). 11 Plaintiffs assert that the evidence in the record shows that at the time of the invention a 12 person of ordinary skill in the art would understand that the phrase “greater than 4 fold 13 increase” had an inherent upper limit of approximately 20-25 fold. (Doc. No. 221 at 18 14 (citing Doc. No. 195-3, Swager Decl. ¶ 42).) But the problem with Plaintiffs’ argument is 15 that Plaintiffs have failed to provide the Court with any authority other than a general 16 citation to Markman holding that the inherent upper limit of an open-ended claim term 17 must be limited to what was known in the art at the time of the invention and would not 18 include changes to that upper limit in the future. Markman does not specifically address 19 this issue. In the absence of such authority, the Court declines to adopt Plaintiffs’ proposed 20 inherent upper limit of about 20-25. 21 Further, the data relied on by Plaintiffs’ expert, Dr. Swager, does not actually support 22 the imposition of an inherent upper limit of about 20-25. In his calculations, Dr. Swager 23 utilizes an extinction coefficient of exactly 2,500,000 for the polymer dye, (Doc. No. 195- 24 3, Swager Decl. ¶ 42), but the portion of the specification where Dr. Swager obtained this 25 number from actually states that the extinction coefficient is “greater than 2,500,000.” (Id. 26 ¶ 41 (citing ’613 Patent at 161:23-162:4).) Thus, Dr. Swager’s calculation is faulty. 27 In sum, the Court adopts Defendants’ proposed construction for this claim term, and 28 the Court rejects Plaintiffs’ proposed construction for this claim term. The Court construes 19 17-cv-01394-H-NLS 1 the term “where the specific signal is at least 3 fold greater than the same antibody 2 conjugated to Pacific Blue” as “a specific signal that is 3 fold or more greater than the 3 signal of the same antibody conjugated to Pacific Blue.”5 4 F. 5 The parties dispute the proper constructions for several chemical structures claimed 6 in the patents at issue. Plaintiffs argue that no construction of these chemical structures is 7 necessary. (Doc. No. 221 at 18.) Plaintiffs argue, in the alternative, that if the Court must 8 add a construction to these chemical structures, the structures should be construed to mean 9 that “the chemical groups referred to have the chemical structures shown and have 10 substitutions at the positions indicated by, for example, R, R’, or R25.” (Id. at 20.) 11 Defendants propose that these chemical structures be construed as “the chemical structure 12 of this unit does not show hydrogen atoms, but the structure as shown is otherwise 13 substituted only where indicated by R, R’, or R25. * = site for covalent attachments to 14 unsaturated backbone.” (Doc. No. 219 at 4.) Certain Chemical Structures 15 Plaintiffs argue that the chemical structures at issue need no construction because 16 line structures such as these are common in organic chemistry and fully convey to chemists 17 the entire structure of the molecule in a simple and easy to understand manner. (Doc. No. 18 221 at 18 (citing Doc. No. 195-3, Swager Decl. ¶¶ 45-48).) But, here, the parties have an 19 apparent dispute regarding whether the claimed structures can include substitutions other 20 than at R, R’, or R25. (Compare Doc. No. 219 at 5 with Doc. No. 221 at 19; Doc. No. 195- 21 3, Swager Decl. ¶ 50.) Because the parties dispute the scope of these claimed structures in 22 their briefing, the Court must resolve the parties’ dispute. See O2 Micro, 521 F.3d at 1361; 23 Eon, 815 F.3d at 1318. 24 The Court begins its analysis of the parties’ dispute by reviewing the claim language. 25 26 27 28 5 The Court slightly alters Defendants’ proposed construction to delete the phrase “no upper limit.” Further, the Court notes that at this time, the Court is merely construing the disputed claim terms from the patents at issue as is proper at the Markman stage of an action for patent infringement. The Court’s decision at claim construction should in no way be interpreted as resolving any potential disputes the parties may have regarding enablement or written description issues. 20 17-cv-01394-H-NLS 1 The claims at issue use chemical line structure drawings to define the scope of the claims. 2 For example, claim 1 of the ’613 patent claims the following chemical structure: “linker L1 3 is” 4 5 6 7 8 9 10 11 ’613 Patent at 232:20-30. In another example, claim 23 of the ’869 patent claims the following chemical structure: “wherein the optional linkers L1 or L2 have the structure:” 12 13 14 15 16 17 ’869 Patent at 249:12-22. The parties’ experts agree that for the claim terms at issue, the 18 terms “R,” “R’,” or “R25” in the claimed structures are substitutions on the chemical 19 structures shown. (Doc. No. 195-3, Swager Decl. ¶ 45 (“the chemical groups . . . have 20 substitutions at the positions indicated by R, R’, or R25”); Doc. No. 195-4, Burgess Decl. 21 ¶¶ 17, 22-23.) Plaintiffs’ expert, Dr. Burgess, concedes that the claimed structures “do[] 22 not literally show substituents at other positions.” (Doc. No. 195-3, Swager Decl. ¶ 50.) 23 Indeed, at the claim construction hearing, Plaintiffs conceded that the literal scope of the 24 claims at issue only permit substitutions at the positions indicated by R, R’, or R25, and 25 they do not permit substitutions at other places. Thus, the claim language supports 26 Defendants’ proposed construction. 27 Plaintiffs argue that an organic chemist would appreciate that other substitutions are 28 possible. (Doc. No. 221 at 19; see also Doc. No. 195-3, Swager Decl. ¶ 50.) But Plaintiffs 21 17-cv-01394-H-NLS 1 fail to support this assertion with any citations to the intrinsic record. Plaintiffs fail to 2 identify any language in the intrinsic record suggesting that other substitutions on the 3 claimed structures at issue are possible. Indeed, at the claim construction hearing, Plaintiffs 4 conceded that substitutions at places other than R, R’, or R25 are not within the literal scope 5 of the claims. As such, the intrinsic record supports Defendants’ proposed construction, 6 not Plaintiffs’ proposal. 7 Plaintiffs also argue that Defendants’ proposed construction is improper because the 8 language “substituted only where indicated by R, R’, or R25” imposes a negative limitation 9 on the claims. (Doc. No. 221 at 19.) But there is no prohibition against the use of negative 10 limitations in claim constructions. 6 See, e.g., Eon, 815 F.3d at 1322-23 (construing the 11 claims in the context of the specification to not cover “utility meters”); In re Gabapentin 12 Patent Litig., 503 F.3d 1254, 1258, 1264-65 (Fed. Cir. 2007) (affirming district court’s 13 construction for the term “adjuvants” that contained a negative limitation explaining that 14 the term “‘[does not] refer to the ingredients of capsule shells or tablet coatings.’”). Here, 15 both parties agree on the scope of the claim terms at issue and agree that the chemical 16 structures at issue only permit substitutions where indicated by R, R’, or R25 and do not 17 permit substitutions elsewhere. Defendants’ proposed construction, which includes the 18 negative limitation “substituted only where indicated by R, R’, or R25,” encompasses that 19 agreement as to claim scope, Plaintiffs’ proposed construction does not. The jury will be 20 aided by a claim construction that provides greater clarity as to the scope of the claims than 21 one that does not. As a result, the Court adopts Defendants’ proposed construction. 22 Further, the latter portion of Defendants’ proposed construction requiring that * = 23 site for covalent attachments to unsaturated backbone is directly supported by both the 24 claim language and the specification of the patents at issue. For example, claims 4, 7, 10 25 and 33 of ’303 provide: “*=site for covalent attachment to [unsaturated] backbone.” ’303 26 27 28 6 Indeed, the Court notes that Plaintiffs in their proposed construction for the claim term “polymer modifying unit,” which the Court has adopted as modified, use a negative limitation. 22 17-cv-01394-H-NLS 1 Patent at 241:60, 244:35, 249:1, 252:50, 257:32; accord ’869 Patent at 237:61, 240:8, 2 243:43, 248:45, 249:24. In addition, the common specification for the patents at issue 3 provides: “*=site for covalent attachment to [unsaturated] backbone.” ’613 Patent at 3:59, 4 4:8, 4:54, 5:11, 8:13, 11:48, 16:15, 25:39, 27:15, 30:40. As such, the latter portion of 5 Defendants’ proposed construction is well supported by the intrinsic record. 6 In sum, the Court adopts Defendants’ proposed construction for these chemical 7 structures, and the Court rejects Plaintiffs’ proposed construction. The Court construes the 8 chemical structures at issue as “the chemical structure of this unit does not show hydrogen 9 atoms, but the structure as shown is otherwise substituted only where indicated by R, R’, 10 or R25. * = site for covalent attachments to [unsaturated] backbone.”7 11 Conclusion 12 For the reasons above, the Court adopts the constructions set forth above. 13 IT IS SO ORDERED. 14 DATED: September 4, 2018 15 MARILYN L. HUFF, District Judge UNITED STATES DISTRICT COURT 16 17 18 19 20 21 22 23 24 25 26 27 28 7 The Court notes that its construction for these chemical structures does not preclude Plaintiffs from arguing infringement under the doctrine of equivalents. “Under the doctrine of equivalents, ‘a product or process that does not literally infringe . . . the express terms of a patent claim may nonetheless be found to infringe if there is “equivalence” between the elements of the accused product or process and the claimed elements of the patented invention.’” Mirror Worlds, LLC v. Apple Inc., 692 F.3d 1351, 1357 (Fed. Cir. 2012) (quoting Warner–Jenkinson Co. v. Hilton Davis Chem. Co., 520 U.S. 17, 21 (1997)). 23 17-cv-01394-H-NLS

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