In Re Glumetza Antitrust Litigation

CourtDistrict Court, N.D. California
DecidedFebruary 3, 2022
Docket3:19-cv-05822
StatusUnknown

This text of In Re Glumetza Antitrust Litigation (In Re Glumetza Antitrust Litigation) is published on Counsel Stack Legal Research, covering District Court, N.D. California primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Glumetza Antitrust Litigation, (N.D. Cal. 2022).

Opinion

1 2 3 4 5 UNITED STATES DISTRICT COURT 6 NORTHERN DISTRICT OF CALIFORNIA 7

8 In re No. C 19-05822 WHA 9 GLUMETZA ANTITRUST No. C 19-05831 WHA LITIGATION. No. C 19-06138 WHA 10 No. C 19-06156 WHA No. C 19-06839 WHA 11 This Document Relates to: No. C 19-07843 WHA

12 No. C 19-05822 WHA (Consolidated) No. C 19-06138 WHA 13 No. C 19-06839 WHA ORDER RE FINAL APPROVAL OF CLASS SETTLEMENTS AND 14 MOTION FOR ATTORNEY’S FEES

15 16 17 INTRODUCTION 18 In this antitrust action, defendant brand and generic manufacturers of a type 2 diabetes 19 drug engaged in a reverse-payment scheme and agreed not to compete with each other by 20 delaying the introduction of a generic version of the drug for several years. On the precipice of 21 trial, the direct-purchaser class reached settlement agreements with all defendants. To the 22 extent stated, the motion for final approval of the settlements is GRANTED. Class counsel’s 23 motion for attorney’s fees and costs is GRANTED IN PART. 24 STATEMENT 25 The order denying summary judgment described the facts of this action in detail (Dkt. 26 No. 537). Briefly, in 2009, pharmaceutical company Depomed, Inc. sued Lupin 27 Pharmaceuticals, Inc. in its various corporate forms for infringing Depomed’s patents on 1 blood sugar levels for individuals suffering from type 2 diabetes. Lupin had entered 2 Depomed’s crosshairs because it had filed an Abbreviated New Drug Application (ANDA) 3 with the FDA, seeking to manufacture and market a generic version of Glumetza. The parties 4 litigated before the Honorable Phyllis J. Hamilton of our district until a claim construction 5 order prompted the parties to settle in February 2012. 6 But this settlement hid an underlying conspiracy from Judge Hamilton — a quid pro quo 7 where Lupin would delay market entry of its generic for four years (until February 1, 2016) 8 and, in return, Depomed paid Lupin $3 million and promised it would not launch an authorized 9 generic to compete with Lupin for one year (until February 2017, atop an FDA-granted 180- 10 day period of market exclusivity) and would also protect Lupin from other generic 11 competition. First, if any other manufacturer succeeded in marketing a generic Glumetza 12 before February 2016, Lupin could market immediately. Second, Depomed covenanted not to 13 license any other generic Glumetza manufacturers until at least 180 days following Lupin’s 14 market entry. 15 The agreement resulted in a windfall for defendants. Depomed had already sold its 16 marketing rights in Glumetza to defendant Santarus, Inc., but then sold its royalty rights to 17 PDL Biopharma in October 2013 (Dkt. No. 464-1). The juiced Glumetza portfolio aided 18 Santarus’ sale to defendant Salix Pharmaceuticals for $2.6 billion in November 2013, and 19 Salix’s sale to defendant Valeant Pharmaceuticals for $14.5 billion in April 2015. Then, in the 20 summer of 2015, Valeant hiked the price of Glumetza on the order of 800%. The wholesale 21 acquisition cost of a 500 mg pill spiked from $5.72 in May to $51.48 by the end of July. At the 22 same time, the cost of a 1000 mg pill rose from $12.37 to $113.36. When Lupin joined the 23 market in February, the supposed-affordable generic did so at around $45 for each 500 mg 24 tablet. 25 Both direct and indirect purchasers started suing in September 2019. The cases were 26 consolidated before the undersigned, the indirect purchasers eventually exited the case, and a 27 direct-purchaser class was certified in August 2020. An order dated May 6, 2021, denied all 1 late July 2021, under the supervision of Judge Donna M. Ryu, the class reached a settlement 2 agreement with Bausch. In August, an order ruled on the parties’ ten Daubert motions, and the 3 final pre-trial conference then occurred over two days, on September 8 and 9. All of the 4 parties’ motions in limine were decided therein. By that point, the class had also reached an 5 agreement with Assertio. Shortly after the hearing on September 8 concluded, the class filed a 6 motion for preliminary approval of the Bausch settlement. Class counsel filed an amended 7 motion for the Bausch settlement on September 14, and a preliminary approval motion 8 regarding the Assertio agreement followed on September 16. On September 20, the class filed 9 a motion for preliminary settlement approval for Lupin, the last to fall. A September 22 order 10 granted preliminary approval to all three settlements. 11 The final approval hearing took place telephonically due to the ongoing COVID-19 12 pandemic. Class counsel notified all class members of the telephonic hearing via the class- 13 action website and via an email from the claims administrator. The docket and the Court 14 calendar also explained how to attend the hearing remotely. The three national wholesalers 15 that had filed a written objection to class counsel’s motion for attorney’s fees participated in 16 the hearing. No other class members joined the call or appeared in the courtroom, which 17 remained open for class members wishing to take part in the hearing. 18 ANALYSIS 19 “The class action device, while capable of the fair and efficient adjudication of a large 20 number of claims, is also susceptible to abuse and carries with it certain inherent structural 21 risks.” Officers for Just. v. Civ. Serv. Comm’n of City & Cty. of San Francisco, 688 F.2d 615, 22 623 (9th Cir. 1982). A settlement purporting to bind absent class members must be fair, 23 reasonable, and adequate. See FRCP 23(e). Rule 23(e)(2) requires district courts to employ a 24 two-step process: First, the parties must show the district court will likely be able to approve 25 the proposed settlement. Second, the district court must hold a hearing to make a final 26 determination of whether the settlement is fair, reasonable, and adequate. We have arrived at 27 step two. 1 Our court of appeals recently explained that the final fairness assessment must analyze 2 the eight Churchill factors: (1) the strength of the plaintiff’s case; (2) the suit’s risk, expense, 3 complexity, and the likely duration of further litigation; (3) the risk of maintaining class action 4 status throughout the trial; (4) the amount offered in settlement; (5) the extent of discovery and 5 the stage of the proceedings; (6) the experience and views of counsel; (7) the presence of a 6 governmental participant (if any); and (8) the reaction of the class members to the proposed 7 settlement. Kim v. Allison, 8 F.4th 1170, 1178–79 (9th Cir. 2021) (quoting In re 8 Bluetooth Headset Prods. Liab. Litig., 654 F.3d 935, 946 (9th Cir. 2011)); Churchill Vill. v. 9 Gen. Elec., 361 F.3d 566 (9th Cir. 2004). Additionally, Rule 23(e)(2) requires the district court 10 to consider an overlapping set of factors, including the adequacy of the notice procedure, “the 11 terms of any proposed award of attorney’s fees,” to scrutinize the settlement for evidence of 12 collusion or conflicts of interest, and to review other, relevant factors before deeming the 13 settlement fair. Kim, 8 F.4th at 1179; Briseño v. Henderson, 998 F.3d 1014, 1023–26 (9th Cir. 14 2021). Among the other relevant factors that will be considered are those listed by this Court 15 in its notice regarding factors to be evaluated for any proposed class settlement, filed herein 16 November 4, 2019 (Dkt. No. 39).

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