MEMORANDUM
I. INTRODUCTION
On November 21, 2003, this Court issued an order allowing the End Payor Plaintiffs’ Motion for Class Certification with respect to two exemplar classes certified under Rule 23(b)(3). Order of 11/21/03 [Doc. No. 168]. This memorandum details the analysis that led to that order.
II. BACKGROUND
This case presents a consolidated action against SmithKline Beecham Corporation and GlaxoSmithKline PLC (collectively “SmithKline”) for violations of the antitrust laws related to its patent for the chemical compound nabumetone, which it sells commercially as “Relafen.” Parties who purchased Relafen from sources other than SmithKline
A. Factual Background
On December 13, 1983, SmithKline received U.S. Patent No. 4,420,639 (the “ ’639
SmithKline filed the patent suits in question on October 27, 1997 (against Copley), November 13, 1997 (against Teva), and February 17, 1998 (against Eon). The three suits were consolidated and tried before Judge Lindsay of this District. On August 14, 2001, Judge Lindsay issued a sixty-seven-page opinion, which held, inter alia, that (1) claims 2 and 4 of the ’639 patent were invalid as anticipated by prior art; and (2) the ’639 patent was unenforceable because of Smith-Kline’s inequitable conduct before the Patent Office. In re ’639 Patent Litig.,
Essentially, the plaintiffs claim that but for SmithKline’s wrongful filing of patent lawsuits, consumers could have begun purchasing nabumetone in a competitive market— comprising both Relafen and its generic alternatives — as early as September 1998. Because of the pending litigation, however, the generic alternatives did not become available until after the stay period terminated and SmithKline’s patent was invalidated. Teva
B. Procedural Background
On February 11, 2003, the end payor plaintiffs filed a consolidated class action complaint against SmithKline. [Doe. No. 68 in Teva Pharm. v. Smithkline Beecham, Civil Action No. 01-12222-WGY]. The lead end payor plaintiffs, on behalf of themselves and other consumers and health benefit providers, asserted claims under federal and state antitrust laws, state unfair competition statutes, and state consumer protection statutes. Compl. II1. On September 16, 2003, the end payor plaintiffs moved for class certification under Federal Rule of Civil • Procedure 23(b)(2) and (3). [Doc. No. 126]. After hearing oral argument, the Court tentatively denied the motion under Rule 23(b)(2) and allowed the motion under Rule 23(b)(3) subject to review of the end payor plaintiffs’ proposed order. See 10/23/03 Hr’g Tr. [Doc. No. 156] at 24. The end payor plaintiffs then submitted a proposed order denying the motion under Rule 23(b)(2), and allowing the motion under 23(b)(3) with respect to the following exemplar class:
Ml persons or entities who purchased and/or paid for Relafen® (known generically as nabumetone) or generic versions of Relafen® in the states of Arizona, California, Florida, Kansas, Maine, Massachusetts, Michigan, Minnesota, New York, North Carolina, Tennessee and Vermont (“the Exemplar States”) during the period February 1, 1992 through and including June 30, 2003 (the [”]Class Period”) for*265 consumption by themselves, their families, or their members, employees, insureds, participants or beneficiaries (the “Class”).
Proposed Order at 1. The end payor plaintiffs’ proposed exemplar class excluded governmental entities, SmithKline and its officers, subsidiaries, and affiliates; persons or entities who purchased Relafen or its generic equivalents directly from SmithKline or its affiliates; persons or entities who purchased Relafen or its generic equivalents for purposes of resale; persons or entities who continued to purchase Relafen after generic equivalents became available for purchase in August 2001; and persons who, under the terms of their third-party health insurance plans, pay the same fixed price for brand-name and generic prescription drugs. Id. The Court examines the terms of the end payor plaintiffs’ proposed order below.
C. Federal Jurisdiction
Having denied certification with respect to the end payor plaintiffs’ federal law claims, see Order of 11/21/03, at 2 (holding that these claims were inappropriate for injunctive relief), this Court nevertheless retains supplemental jurisdiction over the remaining state law claims. 28 U.S.C. § 1367(a). The advanced stages of other actions forming part of the same controversy, including those brought by a separately certified class of direct purchaser plaintiffs, individual drugstore plaintiffs, and a generic manufacturer,
III. DISCUSSION A. Legal Standard
On a motion for class certification, “[a] district court must conduct a rigorous analysis of the prerequisites established by Rule 23.” Smilow v. Southwestern Bell Mobile Sys., Inc.,
Rule 23(a) imposes four “threshold requirements” applicable to all class actions:
(1) the class is so numerous that joinder of all members is impracticable, (2) there are questions of law or fact common to the class, (3) the claims or defenses of the representative parties are typical of the claims or defenses of the class, and (4) the*266 representative parties will fairly and adequately protect the interests of the class.
Fed.R.Civ.P. 23(a); Amchem,
Rule 23(b)(3) permits a class action when common questions “predominate over any question affecting only individual members,” and class resolution is “superior to other available methods for the fair and efficient adjudication of the controversy.” Fed. R.Civ.P. 23(b)(3). Matters “pertinent” to evaluating predominance and superiority include:
(A) the interest of members of the class in individually controlling the prosecution or defense of separate actions; '(B) the extent and nature of any litigation concerning the controversy already commenced by or against members of the class; (C) the desirability or undesirability of concentrating the litigation of the claims in the particular forum; (D) the difficulties likely to be encountered in the management of a class action.
Fed.R.Civ.P. 23(b)(3). This list of pertinent factors is “nonexhaustive.” Amchem,
B. Class Period
Before considering the requirements of Rule 23, the Court addresses the period for which class damages may be claimed. The end payor plaintiffs proposed that the class period run from “February 1, 1992 through and including June 30, 2003.” Proposed Order at 1. They contended that at least with respect to their unjust enrichment claims, “damages could accrue as early as February 1992, when Defendants entered the market under the banner of a patent procured by fraud.” End Payor Pis.’ Proposed Order Reply [Doc. No. 155] at 3. SmithKline responded that the “Class Period cannot possibly begin before December 1998,” the date on which Teva received tentative FDA approval to market generic nabumetone. Defs.’ Proposed Order Opp’n [Doc. No. 152] at 3.
The Court notes that at least as a general matter, entry into the marketplace for branded and generic drugs is governed by the FDA rather than the Patent Office. See Rebecca S. Eisenberg, Lecture, Patents, Product Exclusivity and Information Dissemination 72 Fordham L.Rev. 477, 488 (2003) (discussing the relationship between the legal regimes administered by the FDA and the Patent Office regarding biomedical research and product development, and describing the FDA’s role as a “market gatekeeper”). Accordingly, any profits that SmithKline earned during its initial period of market exclusivity are more properly attributed to the fact that generic competitors lacked FDA approval than to the fact that SmithKline had obtained the ’639 patent. See 21 C.F.R. 314.108 (providing a period of exclusive FDA approval for “new drug products” — such as Relafen). Eon and Teva obtained tentative FDA approval to market their generic nabumetone products on August 8, and December 24, 1998, respectively. Relafen,
C. Rule 23(a)
To satisfy Rule 23(a), the end payor plaintiffs must establish numerosity, commonality, typicality, and adequacy. Amchem,
The end payor plaintiffs have identified a number of common questions, the resolution of which will “affect all or a substantial number of the class members.” Duhaime v. John Hancock Mut. Life. Ins. Co.,
The element of typicality requires that the “named plaintiffs’ claims arise from the same course of conduct that gave rise to the claims of the absent [class] members.” Duhaime,
The adequacy requirement establishes as an “essential prerequisite” to certification that this Court be certain the named end payor plaintiffs will protect the interests of the class. 7A Charles Alan Wright, Arthur R. Miller & Mary Kay Kane, Federal Practice and Procedure § 1765. Before addressing the specific inquiries encompassed by the adequacy analysis, the Court turns to SmithKline’s more general argument that the named end payor plaintiffs’ lack of standing renders them inadequate representatives. Defs.’ Opp’n [Doc. No. 130] at 34-35.
SmithKline asserted that the named end payor plaintiffs, Louise Houchins of California, Tyler Fox of Massachusetts, and Emily Feinberg of Massachusetts, having purchased Relafen or its generic alternatives in only some of the specified states, lacked standing to assert the claims of, or to serve as adequate representatives for, class members who made their purchases in the remaining states. See id. The end payor plaintiffs rejected this challenge as improper
In support of its standing challenge, SmithKline cited In re Terazosin Hydrochloride Antitrust Litigation,
The lower courts in this circuit, however, are bound by no such precedent. Indeed, in Mowbray v. Waste Management Holdings, Inc.,
The approach of Mowbray is consistent with that adopted by several other courts, which have interpreted Supreme Court precedent to direct consideration of class certification issues before those of standing, at least under certain circumstances. See, e.g., Payton v. County of Kane,
The Fifth and Seventh Circuits have interpreted Ortiz to favor a “nuanced approach” for consideration of standing challenges. Linda S. Mullenix, Standing, Nat’l L.J., June 16, 2003, at 43, col. I.
As between the conflicting approaches of the Eleventh Circuit on the one hand, and the Fifth and Seventh Circuits on the other, this Court adopts the latter, finding it more
This flexible, functional standing inquiry also proves consistent with the policies served by class action procedure. See Burns, supra, at 1287-88 (urging the Supreme Court “to acknowledge that the peculiar class-action beast requires a different, and more flexible, standing-and-mootness analysis”). The more traditional inquiry, which under the Eleventh Circuit’s and SmithKline’s interpretation, would require class counsel to identify representatives from each state involved in a multistate class action, would render class actions considerably more cumbersome to initiate, and in turn, less effective in overcoming a lack of incentives to prosecute individual rights and in “aehiev[ing] economies of time, effort, and expense.” Amchem,
Here, adopting the approach of the Fifth and Seventh Circuits, the Court defers consideration of SmithKline’s standing challenge until after certification of the end payor class. Certification is in this case “logically antecedent” because SmithKline’s challenge would not arise but for the proposed certification. Amchem,
Aside from standing, the end payor plaintiffs must establish the two parts of the adequacy inquiry: first, an absence of potential conflict and second, an assurance of vigorous prosecution. See Andrews v. Bechtel Power Corp.,
Finding this reasoning persuasive, the Court concluded that the injured named representatives could not adequately represent the interests of class members who had not suffered similar economic injury.
The Court is aware of at least one decision, Goda v. Abbott Laboratories, No. 01445-96,
In contrast to the plaintiffs in Goda, who moved to certify a class of consumers who purchased branded drugs “in the District,” id. at *3, the end payor plaintiffs in the present action moved to certify a class of consumers who purchased Relafen or its generic equivalent “throughout the United States and its territories.” End Payor Pis.’ Mem. at 1. In light of the additional complexity and problems of manageability presented by the proposed multi-state class, see Amchem,
The Court found more persuasive Goda’s alternative argument that the insured consumer does in fact suffer injury, simply in the future rather than in the past: “[A]l-though copayments and/or premiums may be stabilized for one year, they will surely rise in the next to the detriment of the consumer/beneficiary.” Goda,
In contrast, several other classes of end payors challenged by SmithKline were not excluded. SmithKline asserted that plaintiffs who purchased only branded Relafen— those who purchased Relafen before generic entry but purchased neither Relafen nor generic nabumetone after generic entry (“pre-generic purchasers”), and those who purchased Relafen both before and after generic entry (“brand loyalists”) — suffered no injury. Defs.’ Opp’n at 15-17. With respect to pre-generic purchasers, the end payor plaintiffs emphasized that patients “are bound by the limits of their doctor’s prescription.” End Payor Pis.’ Reply at 17. Patients with prescriptions for Relafen were, prior to August 2001, limited to Relafen “because no substitute drag was on the market.” Id. After August 2001, when generic substitutes entered the market, the end payor plaintiffs estimated that nearly 90 percent of Relafen sales were lost to generic nabumetone. End Payor Pis.’ Reply at 11 (citing Rebuttal Declaration of Raymond S. Hartman (“Hartman Rebuttal Decl.”) [Doc. No. 133] 1126). Given the high likelihood of “switching,” the Court
In contrast to the purchases by pre-generic purchasers, the purchases of brand loyalists may reflect their “conscious choices.”
If, on the other hand, the amount that brand loyalists owed did not vary according to the price of Relafen, but instead varied only with the choice between branded and generic drugs — for example, insured brand loyalists who owed a fixed copayment for branded drugs and a different fixed copayment for generic drugs — the end payor plaintiffs can identify no economic injury. For these brand loyalists, there was no difference between the cost associated with Relafen in the actual versus the but-for world. Brand loyalists whose direct costs did not vary according to the price of Relafen were accordingly excluded from the end payor plaintiff
With the class limited as described above, the Court determined that no potential conflicts existed. With respect to the second element of the adequacy inquiry, the Court notes the considerable class action experience of the firms appointed co-lead counsel: Milberg Weiss Bershad Hynes & Lerach LLP; Spector, Roseman & Kodroff, P.C.; Miller Faueher and Cafferty LLP; and Heins Mills & Olson, P.L.C. At least one of these firms has represented classes of end payors in actions involving analogous claims of delayed generic entry. See e.g., Warfarin,
D. Rule 23(b)(2)
Rule 23(b)(2) permits a class action when the Court may fashion “appropriate final in-junctive relief or corresponding declaratory relief with respect to the class as a whole.” Fed.R.Civ.P. 23(b)(2). The plaintiffs asserted that SmithKline’s “continuing unlawful acts of monopolization ... threaten continuing harm to all Class members,” entitling them not only to damages, but also to an injunction preventing Smithkline from acquiring and maintaining a future monopoly. End Payor Pis.’ Mem. at 6. SmithKline contended that this “ill-defined prayer,” — merely a “thinly veiled attempt to make an end run around Illinois Brick [v. Illinois,
As an initial matter, the lower courts that have addressed the issue have held that claims for injunctive relief under Section 16 of the Clayton Act, 15 U.S.C. § 26, do not undermine Illinois Brick, but rather fall properly outside its scope. See e.g., Mid-West Paper Prods. Co. v. Continental Group,
Obviously, the risk of exposure to multiple liability, the difficulty in tracing the allocation of the overcharge among different levels of purchasers, and the general desirability of symmetrical application of the pass-on theory to plaintiffs and defendants are wholly unrelated to the issue whether a party should be entitled to sue for injunc-tive relief. Nor does the position taken in Illinois Brick, that effective enforcement of the antitrust laws requires that only direct purchasers be permitted to sue for treble damages, have validity in the context of [§ ] 16.... With respect to injunc-tive relief, ... the entitlement of one group to sue does not diminish the incentive of another group to sue.
Id. at 592.
Yet even assuming their standing, the end payor plaintiffs must also demonstrate “threatened loss or damage by a violation of the antitrust laws.” 15 U.S.C. § 26. The Supreme Court has held that this requirement is satisfied by a showing of “significant threat of injury from an impending violation of the antitrust laws or from a contemporary violation likely to continue or recur.” Zenith Radio Corp. v. Hazeltine Research, Inc.,
E. Rule 23(b)(3)
Certification under Rule 23(b)(3) requires that common questions “predominate” over individual questions, such that class treatment is “superior” to other methods of resolution. Fed.R.Civ.P. 23(b)(3); see also Tardiff v. Knox County,
1. Predominance
To establish predominance under Rule 23(b)(3), the end payor plaintiffs must dem
a. Impact
As an initial matter, the Court emphasizes that the end payor plaintiffs’ claims for damages and restitution arise solely under state law. Compl. HH 3^4. In contrast to federal antitrust law, see Illinois Brick,
Under both federal and state law, the essential elements of a private antitrust action are the same: proof of a violation by the defendant, a demonstration of injury to the plaintiff, and an approximation of the plaintiffs damages. See, e.g., Bell Atlantic Corp. v. AT & T Corp.,
In relation to the first and third elements discussed above, the second element of the
Yet even assuming that these decisions interpreting federal antitrust law would be otherwise persuasive, but see, e.g., 7B Wright, Miller & Kane, supra, § 1781 (cautioning that “although many courts have certified antitrust suits under Rule 23(b)(3), certification is not always appropriate”), the Court must examine the end payor plaintiffs’ claims under governing state law. As emphasized above, state law defines the elements of the end payor plaintiffs’ claims and in turn, proves relevant to determining the demonstration of common injury necessary for certification. See William H. Page, The Limits of Indirect Purchaser Suits: Class Certification in the Shadow of Illinois Brick, 67 Antitrust L.J. 1, 27 (1999); cf. Windham v. American Brands, Inc.,
b. Governing State Law
The Court begins by acknowledging that federal appellate courts have viewed class actions governed by the law of multiple states with serious skepticism. See, e.g., In re Bridgestone/Firestone, Inc.,
First, they contended that “[bjecause SKB is based in Pennsylvania, the Court could also apply Pennsylvania law to the entire Class.” End Payor Pis.’ Mem. at 8 n. 9. Because state antitrust, consumer protection, and unjust enrichment laws vary on such issues as prohibited practices and limitations periods, see, Section III.E.l.b.ii-iv, infra, this Court must determine if Pennsylvania has a “significant contact or significant aggregation of contacts” to this litigation that would justify the application of its law over the various laws of other states. Phillips Petroleum Co. v. Shutts,
By definition, the sales at issue in this litigation did not involve SmithKline or its Pennsylvania location. See Proposed Order at 1 (excluding from the proposed class persons or entities who purchased Relafen or its generic equivalents directly from Smith-Kline). Rather, many — if not most — of the relevant sales took place wholly outside Pennsylvania, between out-of-state direct purchasers, see Valley Drug,
In the alternative, the end payor plaintiffs argue that “[e]ven if the law of multiple states must be applied, the laws governing the classes’ antitrust, consumer protection, and unjust enrichment claims reveal ‘no significant conflict.’ ” End Payor Pis.’ Mem. at 17. As an initial matter, the Court must determine whether the “law of multiple states” must in fact be applied. Both Massachusetts and Pennsylvania
This fact alone, however, does not necessarily defeat certification. Indeed, this Court has previously certified a class of plaintiffs whose claims were governed by the laws of several states. Mowbray,
A. Standing
As stated above, each of the exemplar states permits indirect purchaser actions under its antitrust, consumer protection, or unfair trade practices statutes.
In addition to these statutory causes of action, each of the exemplar states recognizes a cause of action for unjust enrichment. Murdock-Bryant Constr., Inc. v. Pearson,
Notwithstanding these commonalities, the laws of certain exemplar states incorporate variations that counsel against certification. These variations are the subject of the discussion below. As a general matter, the Court considered statutory and common law claims asserted under the laws of the same state as a pair. Accordingly, if variations between state laws required excluding statutory claims raised under the laws of State A, equitable claims raised under the laws of State A were also excluded. The Court concluded that a contrary approach would be inconsistent with the requirements of adequacy and superiority. To the extent that a judgment in this action would be claim pre-clusive, including State A equitable claims would effectively waive State A statutory claims, raising adequacy concerns for end payors who might prefer to litigate their statutory claims individually or as part of a State A class. See Clement v. American Honda Fin. Corp.,
B. Individual Injury
As stated above, the second element of the end payor plaintiffs’ antitrust claims— demonstration of injury — warrants special scrutiny. State courts have differed significantly in their consideration of this element, prompting one commentator to observe: “The most important determinant of class certification of indirect purchaser suits appears to be where the suit is filed.” Page, supra, at 21; compare, e.g., Bellinder v. Microsoft Corp., Nos. 00-C-0855, 00-C-00092, 99CV17089,
In contrast, several other courts have denied class certification after concluding that their states’ indirect purchaser statutes, unlike the District of Columbia’s, require proof of injury to each class member. In Execu-Tech Business Systems, Inc. v. Appleton Papers Inc.,
In Melnick v. Microsoft Corp., Nos. CV-99-709, CV-99-752,
Michigan courts have declined to certify indirect purchaser classes on four occasions. See A & M Supply,
In Gordon v. Microsoft Corp., No. 00-5994,
The above decisions suggest that these courts have interpreted their respective indirect purchaser statutes with a more “skeptical view” of antitrust policies and remedies. See Page, supra, at 17.
The end payor plaintiffs have not made such a showing. Rather, they rely on the declarations of Raymond S. Hartman (“Dr. Hartman”), an economist who proposes methodologies “potentially available to calculate damages of the Class on an aggregate basis.” End Payor Pis.’ Mem. at 15. Specifically, Dr. Hartman discusses the “top-down” method, which would trace but-for and actual prices from SmithKline down to end payors, the “bottom-aeross” method, which would compare but-for and actual prices paid by end payors at the bottom of the distribution chain, and a hybrid version “making use of the most reliable components of each method.” Hartman Decl. 1123. Although these methods are “aimed at estimation of aggregate class-wide overcharge damages,” Dr. Hartman asserts that they can also be applied to specific groups or individuals to “differentiates] and allocate] damages.” Id. K25. He does not, however, go further toward differentiating or allocating damages based on, for example, the unique characteristics of various states’ markets or consumers. In fact, in response to SmithKline’s objection, Dr. Hartman states: “It is my understanding that the formulaic methods ... must provide a sufficiently accurate calculation of aggregate damages. At this stage of the litigation, it is unnecessary that I calculate individual damages to each and every Class member.” Hartman Rebuttal Deck H10 (emphasis in original). More significantly, none of Dr. Hartman’s proposed methods demonstrates individual impact to members of the end payor plaintiffs’ classes. See also Defs.’ Opp’n, Ex. 3 (Hartman Dep.) at 93:10-93:16 (A: “Well, there has been a different — there has been different quanta of effects for different class members and some of those quanta for certain purchasers are zero and they’re the ones you’re identifying.” Q: “How will you identify those people?” A: “This report doesn’t go after that.”).
Because the end payor plaintiffs had not made the stronger showing deemed necessary under the indirect purchaser statutes of Florida, Maine, Minnesota, and Michigan, end payor plaintiffs from these states were excluded from the exemplar classes,
i) Unilateral Monopolies
In addition to the “skeptical” interpretations discussed above — which some might describe as differences “in nuance,” In re Rhone-Poulenc Rorer Inc.,
Under California law, a challenge to unilateral conduct does not state a cognizable antitrust claim. See Dimidowich v. Bell & Howell,
Although “broad and undeveloped by case law,” Bergstrom v. Noah,
The Tennessee Trade Practices Act, Tenn.Code Ann. § 47-25-101, declares the following anticompetitive conduct to be “against public policy”: “all arrangements, contracts, agreements, trusts, or combinations between persons or corporations designed, or which tend, to advance, reduce, or control the price or the cost to the producer or the consumer of any such product or article.” Id. (emphasis added). None of these terms appears to include unilateral conduct. See 6 Julian 0. von Kalinowski, Antitrust Laws and Trade Regulation § 116.03 (2d ed.2003). The end payor plaintiffs also allege violations of the Consumer Protection Act, Tenn.Code Ann. §§ 47-18-101 to — 108. Compl. U 102(u). Although modeled after the Federal Trade Commission Act, the Tennessee Consumer Protection Act differs in one significant respect: unlike the federal provision, which prohibits both unfair methods of competition and unfair or deceptive acts or practices, the Tennessee statute prohibits only unfair or deceptive acts or practices. Sherwood v. Microsoft Corp., No. M2000-01850-COA-R9-CV,
This history makes clear that by the time Tennessee adopted its Consumer Protection Act, its drafters and the legislators considering it had the benefit of the federal act and experience under it, the proposed Uniform Trade Practices Act and Consumer Protection Law, the statutory language adopted in many other states, and the evaluations of a number of authors of learned articles and treatises. We cannot presume other than that the Tennessee General Assembly knowingly chose not to include antitrust or anticompetitive conduct as actionable under the TCPA.
Id. at *32. Because neither of their statutory claims is cognizable under state law, end payors from Tennessee were included in the exemplar classes with respect to their claims for unjust enrichment only.
ii) Restrictions on Remedies
Under New York law, “an action to recover a penalty ... imposed by statute may not be maintained as a class action” unless the statute imposing the penalty “specifically authorizes” class recovery. N.Y. C.P.L.R. 901(b). For purposes of this rule, the treble damages permitted by the New York antitrust statute, N.Y. Gen. Bus. Law §§ 340-347 (the “Donnelly Act”), have been deemed a “penalty.” Asher v. Abbott Labs.,
It is not, however, completely clear that C.P.L.R. 901(b) ought be applied by federal courts. But see In re Microsoft Corp. Antitrust Litig.,
On its face, Rule 23 “merely establishes the procedures for pursuing a class action in the federal courts.” Wade v. Danek Med., Inc.,
Here, C.P.L.R. 901(b) expresses a state interest in avoiding “annihilatory punishment” by discouraging multiple recoveries of statutory penalties. See Lennon v. Philip Morris Cos., Inc.,
Because it found no “direct collision” between the state and federal provisions, the Court’s decision whether to apply C.P.L.R. 901(b) was guided not by Hanna, but by the “twin aims of the Erie rule: discouragement of forum-shopping and avoidance of inequitable administration of the laws.” 19 Wright, Miller & Cooper, supra, § 4504 (quoting Hanna,
The Court’s application of C.P.L.R. 901(b) does not, however, necessarily bar the end payor plaintiffs’ claims under the New York consumer protection act, N.Y. Gen. Bus. Law § 349. Compl. 11102(q). Under Section 349(h), private plaintiffs may recover actual damages, a statutory minimum, or up to treble damages if the court finds a willful or knowing violation. N.Y. Gen. Bus. Law § 349(h). As with the Donnelly Act, because this Section does not “specifically authorize” class recovery, C.P.L.R. 901(b) bars class claims for minimum or treble damages. Super Glue Corp. v. Avis Rent A Car Sys., Inc.,
Yet bringing such an action requires named plaintiffs to waive their claims to minimum and treble damages. See id.; Burns v. Volkswagen of Am., Inc., 118 Mise.2d 289,
Nor are the Court’s concerns lessened because “any class member wish[ing] to pursue his or her statutory right to minimum and treble damages ... may opt out of the class.” Super Glue Corp.,
iii) Direct Benefit
Under North Carolina law, “to establish a claim for unjust enrichment, a party must have conferred a benefit” that was “consciously accepted” by the defendant. Booe,
Linda Pyles received title to the property through her husband. Although he had previously acquired his interest in this property with plaintiffs assistance, this does not satisfy plaintiffs burden of showing that she conferred a benefit directly on defendant Linda Pyles.
The end payor plaintiffs have similarly failed to satisfy this burden. Any enrichment that SmithKline received was conferred more directly by pharmaceutical wholesalers than by end payors, who by definition purchased Relafen from sources other than SmithKline. Proposed Order at 1. Moreover, as in Effler, the fact that many pharmaceutical wholesalers passed on and in fact benefit-ted from the overcharges paid by end payors, see Valley Drug,
After thus limiting the exemplar classes to account for differences in state law, the Court concluded that the end payor plaintiffs had demonstrated the predominance of common issues for the remaining class members. The Court accordingly turned to superiority, the final requirement of Rule 23.
2. Superiority
As stated by the Supreme Court in Amchem, the requirement of superiority, like that of predominance, ensures that resolution by class action will “achieve economies of time, effort, and expense, and promote ... uniformity of decision as to persons similarly situated, without sacrificing procedural fairness or bringing about other undesirable results.” Amchem,
The Advisory Committee’s core concern was particularly compelling here, where protection of the public depends upon vigorous private enforcement of state laws but the small size of individual claims renders such enforcement unlikely. See Hartman Deck, tbl. 2 (documenting differences between branded and generic prices that range from $0.35 to $1.21 per pill); Bronsteen & Fiss, supra, at 1419 (“The most compelling [use of the class action] occurs when someone inflicts a small harm on each member of a large group of people.”); cf. Illinois Brick,
Turning now to the pertinent factors identified in Rule 23(b)(3), the Court emphasizes
As in most multi-state class actions, potential “difficulties likely to be encountered in the management of’ this action, Fed.R.Civ.P. 23(b)(3)(D), posed a more serious concern. See Szabo v. Bridgeport Machs., Inc.,
IV. CONCLUSION
For the foregoing reasons, the End Payor Plaintiffs’ Motion for Class Certification [Doc. No. 119] was ALLOWED in part and DENIED in part. The motion was DENIED under Rule 23(b)(2), and ALLOWED under Rule 23(b)(3) for the following exemplar classes:
With respect to their antitrust and consumer protection claims—
All persons or entities who purchased Relafen or its generic alternatives in the states of Arizona, California, Massachusetts, or Vermont during the period of September 1, 1998 through June 30, 2003 for consumption by themselves, their families, members, employees, insureds, participants, or beneficiaries,
and with respect to their unjust enrichment claims—
All persons or entities in the United States who purchased Relafen in the states of Arizona, California, Massachusetts, Tennessee, or Vermont during the period September 1, 1998 through June 30, 2003 for consumption by themselves, their families, members, employees, insureds, participants, or beneficiaries.
Excluded from both classes were governmental entities; SmithKline and its officers, directors, management, employees, subsidiaries, and affiliates; persons or entities who purchased Relafen for purposes of resale; and persons or entities who purchased Relafen directly from SmithKline or its affiliates.
Notes
. Parties who purchased Relafen directly from SmithKline ("direct purchasers") also moved for class certification. The direct purchasers' motion was discussed in In re Relafen Antitrust Litig.,
. Unless otherwise indicated, these facts are drawn from the Court's Memorandum and Or
. Under the Local Rules for the Federal Circuit, unpublished decisions are not to be cited as precedent, but may be relied upon in asserting "claim preclusion, issue preclusion, judicial es-toppel, law of the case, or the like.” Fed. Cir. R. 47.6(b).
. Teva acquired Copley (and its generic nabume-tone products) in August 1999.
. The fact that these actions have now settled, see Order of 2/13/04 [Doc. No. 286]; Order of 2/13/04 [Doc. No. 62 in Eon Labs., Inc. v. Beec-ham Group PLC, Civil Action No. 03-10506-WGY], does not alter the Court's analysis, because the progress of the present action is now-sufficiently advanced to counsel against declining jurisdiction. See, e.g., Order of 11/21/03 (specifying the form of notice); Order of 2/18/04 (directing that notice be provided to the end payor plaintiffs’ class).
. In its separate action, Eon asserted that it could have filed its abbreviated new drug application as early as December 24, 1996. Am. Compl. [Doc. No. 74] 1151. Yet in support of this assertion, Eon explained only that Smith-Kline’s "sham Orange Book listing [of the ’639 patent]” and "malicious Sham Infringement Action” resulted in thirty-month stay periods (the earliest of which was triggered in September 1997), and a subsequent 180-day "Generic Exclusivity Period” (which was triggered in August 2001). See id. 111129, 51-54. Neither of these periods account for the fact that the first applications, filed not by Eon, but by Copley and Teva, were not filed until August 1997. See Compl. V 52(a) — (b).
. Mullenix contrasts the "nuanced” approach of the Fifth and Seventh Circuits with the "restrictive” rule observed by other courts, which "prevents review of [all] standing challenges prior to the class certification decision.” Mullenix, supra. Because this Court finds deferral of SmithKline's standing challenge appropriate even under the approach of the Fifth and Seventh Circuits, it need not address this distinction.
. The Court notes that Valley Drug identified a conflict between direct purchasers who benefit from generic delay versus those who were injured, a conflict arguably different from — and more serious than — that between end payors who were not injured by generic delay versus those who were. Indeed, in contrast to the direct purchasers of Valley Drug, the end payor plaintiffs here might be characterized as uniformly "not benefitted.” Yet this superficial uniformity would not imply uniformity of economic interests. With respect to settlement, for example, an uninjured end payor might be willing to accept a far lesser sum than would an injured end payor with an entirely different economic situation.
. The Court could imagine, for example, discounting the damages to account for the probability of non-switching.
. The Court assumes that consumers who continued to choose Relafen in the actual world would have done so in the but-for world — that is, even if generic nabumetone had become available in August 1998 rather than August 2001. This assumption is admittedly imperfect: Consider, for example, consumers who continued purchasing Relafen after generic entry, but only because they were reluctant to switch after starting treatment with the branded drug. Had generic alternatives been available earlier, such consumers might have started with and continued purchasing generic nabumetone rather than Relafen. The Court nevertheless excludes such consumers because identifying them would require the sort of individualized inquiries that would render class certification inappropriate. See Cardizem,
. A similar analysis applies to consumers who purchased only generic nabumetone. See Defs.’ Proposed Order Opp'n at 4. Consumers whose costs varied according to the price of generic nabumetone were injured by what the end payor plaintiffs allege were artificially inflated prices. See End Payor Pis.' Mem. at 1. Consumers whose costs did not vary according to the price of generic nabumetone were not injured and were accordingly excluded from the end payor plaintiff classes.
. Under this test, patients who were first prescribed Relafen after August 1998 — the date of generic entry in the but-for world — were not excluded from the end payor plaintiff classes. That these patients might not have been prescribed Relafen in the but-for world, see Defs.' Opp'n at 19 (asserting a probable decline in prescriptions because SmithKline would have ceased its promotion of Relafen upon generic entry), does not change the fact that they were prescribed Relafen in the actual world and therefore suffered economic injury.
. In a more recent decision, the Supreme Court explained, consistent with the Third Circuit’s view, that the indirect purchaser rule is applied to claims for money damages to "eliminate the complications of apportioning overcharges,” "eliminate multiple recoveries," and "promote the vigorous enforcement of the antitrust laws.” Kansas v. UtiliCorp United, Inc.,
. One of the cases consolidated in this action was transferred from the Eastern District of Pennsylvania, see Twin Cities Bakery Workers Health & Welfare Fund v. SmithKline Beecham Corp., No. 02-CV-985 (E.D. Pa. filed 2002), and therefore requires application of Pennsylvania’s choice of law rules. See Van Dusen v. Barrack,
. The fact that the exemplar states have recognized indirect purchaser actions brings the present claims out from under "[t]he [l]ong [s]hadow of Illinois Brick." Terazosin, 160 F.Supp.2d at 1372. Unlike states that have adopted the Illinois Brick prohibition, the exemplar states have not expressed a policy against indirect purchaser actions that might otherwise be undermined by the end payor plaintiffs' present claims.
. See Cole v. Hewlett Packard Co.,
. To be sure, there are variations in states' definitions of unjust enrichment. As examples, SmithKline cites differences in the conduct required and the availability of equitable defenses. See Defs.' Opp'n at 31-32. Yet with the exception of the variation discussed below, see Section III.E.l.b.v, infra, such differences prove largely irrelevant. As the end payor plaintiffs note, the conflict between states that require illegal conduct and those that do not is “immaterial ... because Plaintiffs here do allege unlawful conduct." End Payor Pis.’ Reply at 32. Similarly, although states may "vary significantly in the requirements necessary to establish the defense [of unclean hands]," Lilly v. Ford Motor Co., No. 00 C 7372,
. Certainly, the denials of certification also reflect other factors. See e.g., Gordon,
. In so excluding the Kansas plaintiffs, the Court makes no comment on the validity of the end payor plaintiffs' previously asserted claim of fraudulent concealment. See Relafen,
. Although Tennessee courts have required that unjust enrichment plaintiffs first exhaust their legal remedies, see Paschall's Inc. v. Dozier,
. In an unpublished opinion, the Fourth Circuit suggested that on different facts, North Carolina courts adopt "a broader approach to unjust enrichment than is indicated by Effler's 'direct benefit’ rule.” Metric Constructors, Inc. v. Bank of Tokyo-Mitsubishi, Ltd.,
