In re Relafen Antitrust Litigation

231 F.R.D. 52, 2005 U.S. Dist. LEXIS 21630, 2005 WL 2386119
District Court, D. Massachusetts·Decided September 28, 2005·No. No. 01-12239-WGY·Published·Cited by 37 cases

Opinion

MEMORANDUM

YOUNG, Chief Judge.

I. INTRODUCTION

A. General Considerations

This is a nationwide consumer class action. The Court has certified an expanded fifty-state class solely for the purpose of settlement. See Amckem Prods., Inc. v. Windsor, 521 U.S. 591, 620, 117 S.Ct. 2231, 138 L.Ed.2d 689 (1997) (certifying a class for settlement purposes only). Before the Court may approve this class action settlement, it must find that the settlement “is fair, reasonable, and adequate.” Fed.R.Civ.P. 23(e)(2). As explained in the Manual for Complex Litigation:

[T]he judge is required to scrutinize the proposed settlement to ensure that it is fair to the persons whose interests the court is to protect. Those affected may be entitled to notice and an opportunity to be heard. This usually involves a two-stage procedure. First, the judge reviews the proposal preliminarily to determine whether it is sufficient to warrant public notice and a hearing. If so, the final decision on approval is made after the hearing.

Manual for Complex Litigation, Fourth § 13.14 at 171 (footnotes and citations omitted).

[58]*58The judicial role in reviewing a proposed settlement is critical ____ Even after notice of a proposed settlement is sent, a judge’s statement of concerns about the settlement during the fairness hearing might stimulate the parties to renegotiate in order to avoid possible rejection by the judge. If the fairness hearing leads to substantial changes adversely affecting some members of the class, additional notice, followed by an opportunity to be heard, might be necessary.
To determine whether a proposed settlement is fair, reasonable, and adequate, the court must examine whether the interests of the class are better served by the settlement than by further litigation. Judicial review must be exacting and thorough. The task is demanding because the adver-sariness of litigation is often lost after the agreement to settle. The settling parties frequently make a joint presentation of the benefits of the settlement without significant information about any drawbacks. If objectors do not emerge, there may be no lawyers or litigants criticizing the settlement or seeking to expose flaws or abuses. Even if objectors are present, they might simply seek to be treated differently than the class as a whole, rather than advocating for class-wide interests. The lack of significant opposition may mean that the settlement meets the requirements of fairness, reasonableness, and adequacy. On the other hand, it might signify no more than inertia by class members or it may indicate success on counsel’s part in obtaining, from likely opponents and critics, agreements not to object. Whether or not there are objectors or opponents to the proposed settlement, the court must make an independent analysis of the settlement terms.

Id. at 309-10 (footnote and citations omitted). This memorandum addresses these issues.

B. This Case

This case presents a consolidated action against SmithKline Beecham Corporation and GlaxoSmithKline PLC (collectively “SmithKline”) for violations of antitrust laws in connection with its patent for the chemical compound nabumetone — which is sold commercially as “Relafen.” Parties who purchased Relafen from sources other than SmithKline for purposes other than resale (the “End Payors” or “End Payor Plaintiffs”) move for final approval of the proposed settlement pursuant to Federal Rule of Civil Procedure 23(e). End Payor Pis.’ Mem. of Law in Supp. of Final Approval of Proposed Settlement (“End Payors’ Mem.”) [Doc. No. 415].

The class plaintiffs — individual consumers, health care plans, and insurers — are seeking damages incurred as a result of SmithKline’s alleged misrepresentations made in their successful pursuit of a patent for nabumetone. See Consolidated Class Action Compl. on Behalf of Nationwide End-Payor Class [No. 01-CV-12222, Doc. No. 68] (“Class Action Compl.”) ¶¶ 34-84.

On November 24, 2004, this Court preliminarily certified a settlement class consisting of consumers and third party payors. Order Granting Preliminary Approval of Settlement, Certifying Class for Purposes of Settlement, Directing Notice to the Class, and Scheduling Fairness Hearing (“Preliminary Approval Order”) [Doc. No. 373] (dated November 24, 2004). It also granted initial approval to a proposed settlement agreement between SmithKline and “[a]ll persons or entities in the United States who purchased Relafen and/or its generic alternatives (known as nabumetone) during the period of September 1, 1998 through June 30, 2003.” Id. The parties now seek final approval of the settlement, permanent certification of the class, award of a cy pres award, and entry of final judgment. In addition, class counsel seeks attorney’s fees, costs, and incentive awards for the named plaintiffs.

A fairness hearing was held before this Court on May 4, 2005. A number of objectors 1 were permitted to intervene as objec[59]*59tors to the settlement, each of .whom participated in the hearing through retained counsel. See Tr. of H’rg of 5/4/05. Having considered the evidence presented at the hearing, all objections, the arguments of counsel, additional briefs allowed by this Court, and the full record of the case, the Court grants the motion for final certification of the class, and approves the proposed settlement. Moreover, the Court grants the End Payors’ Joint Petition for Attorney’s Fees, Reimbursement of Expenses and Incentive Awards to the Named Plaintiffs [Doc. No. 419] in its entirety.

II. BACKGROUND

A. Factual Background2

On December 13, 1983, after its initial rejection, the United States Patent and Trademark Office (the “Patent Office”) issued SmithKline United States Patent No. 4,420,639 (the “’639 patent”) for the compound nabumetone, a non-steroidal anti-inflammatory drug also described as methoxy ketone. In re ’639 Patent Litig., 154 F.Supp.2d 157, 169 (D.Mass.2001) (Lindsay, J.).3 In, February of 1992, after receiving approval from the Food and Drug Administration (the “FDA”), SmithKline commenced commercial sales of the patented compound under the brand name Relafen. See id. at 159.

In August and December of 1997, Copley Pharmaceutical, Inc. (“Copley”), Teva Pharmaceutical Industries, Ltd. and Teva Pharmaceuticals USA (“Teva”), and Eon Laboratories, Inc. (“Eon”) filed abbreviated new drug approvals, or ANDAs, with the FDA seeking approval to market generic nabume-tone products. In re Relafen Antitrust Litig., 221 F.R.D. 260, 264 (D.Mass.2004); In re ’639 Patent Litig., 154 F.Supp.2d at 160. In each of their applications, the generic drug manufacturers certified that the ’639 patent was, to the best of their knowledge, invalid or unenforceable. See In re ’639 Patent Litig., 154 F.Supp.2d at 160.

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In re Relafen Antitrust Litigation, 231 F.R.D. 52, 2005 U.S. Dist. LEXIS 21630, 2005 WL 2386119 (D. Mass. 2005).

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