In Re Gabapentin Patent Litigation

407 F. Supp. 2d 607, 2005 WL 3597691
District Court, D. New Jersey·Decided December 27, 2005·No. MDL No. 1384, 00-2931(JCL), 00-2931, 00-3522, 00-4168, 00-4589, 00-6073, 01-0193, 01-0611, 01-1537, 01-2194, 03-1545, 03-1824, 03-4017, 04-2859, 04-4789·Published·Cited by 1 cases

Opinion

MEMORANDUM AND ORDER

LIFLAND, Senior District Judge.

Before the Court is FirsL-Wave Defendants’ 1 Motion to Bar Kaye Scholer LLP From Appearing as Attorneys for Plaintiffs. For the reasons set forth below, First-Wave Defendants’ motion is granted.

BACKGROUND

This motion to bar the law firm of Kaye Scholer from appearing on behalf of plaintiffs in this multidistrict patent infringement action (the “Gabapentin action”) stems from the side-switching activities of two current Kaye Scholer attorneys, Scott G. Lindvall and Patricia J. Clarke, formerly of Darby & Darby (“Darby”). At the *609 time of their association with Darby, Mr. Lindvall and Ms. Clarke were primarily responsible for the representation of Defendant Ivax Corporation (“Ivax”) in the Gabapentin action.

In February 2001, the Judicial Panel on Multidistrict Litigation issued an Order consolidating the patent infringement liti-gations against the First-Wave Defendants before this Court. Shortly thereafter, the First-Wave Defendants entered into a written Joint Defense and Confidentiality Agreement (“JDA”) which recognized, inter alia, that the sharing of confidential information, including attorney work-product, would be in the best interests of all defendants to efficiently manage the defense of this litigation. Mr. Lind-vall, then a partner at Darby & Darby, executed the JDA on behalf of Ivax.

Mr. Lindvall and Ms. Clarke, Senior Counsel to Darby, were involved in the defense of the Gabapentin action. According to Ivax and the other First-Wave Defendants, Mr. Lindvall and Ms. Clarke were privy to confidential attorney work-product and privileged information relating not only to Ivax, but to all FirsL-Wave Defendants: Mr. Lindvall and Ms. Clarke established and executed defense strategy; collected both testimonial and documentary evidence from Ivax’s employees and files; and analyzed legal issues in preparation for summary judgment motions. They also participated regularly in joint defense meetings and conference calls where counsel for all First-Wave Defendants freely discussed their strategies for conducting the litigation, including formulating invalidity and noninfringement defenses and discovery strategies, evaluating expert reports, and drafting First-Wave Defendants’ joint statement of facts and motions regarding the production of documents from Warner-Lambert’s privilege log. (Declaration of Steven D. Rubin, Esq., ¶ 4; Declaration of Steven M. Amundson, Esq., ¶ 11; Declaration of Paul J. Molino, Esq., ¶ 8; Declaration of Stanley H. Lieberstein, Esq., ¶ 10) Neither Pfizer, Kaye Scholer, nor Mr. Lindvall and Ms. Clarke dispute that Mr. Lindvall and Ms. Clarke were fully engaged in and primarily responsible for the pretrial representation of Ivax, and in the course thereof, were privy to confidential attorney work-product and privileged information relating to all FirsLWave Defendants.

Darby’s representation of Ivax ceased in June 2003. In March 2005, Mr. Lindvall sought to join Kaye Scholer as a partner. Mr. Lindvall recommended to Kaye Scho-ler that the firm also hire Ms. Clarke. Kaye Scholer, at the time, did not represent Pfizer in the Gabapentin action, but did represent Pfizer in In re Neurontin Antitrust Litigation, 217 F.Supp.2d 1380, pending in this Court. Kaye Scholer was aware of the possibility that Pfizer might ask the firm to represent it in the Gaba-pentin action. (Sherman Decl. ¶ 2)

During the course of Kaye Scholer’s evaluation of Mr. Lindvall’s and Ms. Clarke’s candidacies, it became known that they had previously represented Ivax in the Gabapentin action on behalf of Darby. Accordingly, Mr. Lindvall was advised that any partnership offer was contingent upon Kaye Scholer obtaining appropriate waivers by Ivax of any conflict arising out of Kaye Scholer’s representation of Pfizer in both the Neurontin matter and the Gaba-pentin action. Ms. Clarke was similarly informed that a job offer depended on Ivax executing a waiver. (Sherman Deck ¶ 4)

In seeking to obtain these waivers, Milton Sherman, Esq., partner and co-chair of the Patent Group at Kaye Scholer, contacted William Mentlik, Esq., Ivax’s outside counsel. Mr. Sherman explained that Kaye Scholer wanted to add Mr. Lindvall as a partner, subject to an appropriate *610 ethical screen. Mr. Sherman asked if Ivax would be willing to waive any right to assert a conflict of interest against Kaye Scholer based on Mr. Lindvall joining the firm, with appropriate screening. Mr. Mentlik agreed to discuss the matter with Ivax’s general counsel, Steven D. Rubin, Esq., and indicated that he would recommend that Ivax agree to the request for a waiver. (Sherman Decl. ¶ 5) A similar discussion regarding Ms. Clarke took place several weeks later.

By letter dated April 14, 2005, Mr. Sherman proposed the following arrangement:

Mr. Lindvall, after joining Kaye Scho-ler, will not work on either the Neuron-tin or the Gabapentin Matter, any of the individual actions included within those matters, or any FDA issue relating to Neurontin or gabapentin. In addition, Kaye Scholer will create an ethical screen between Mr. Lindvall and the Kaye Scholer attorneys and personnel representing Pfizer in both the Neuron-tin and Gabapentin Matters and any FDA issues relating to Neurontin and Gabapentin.
IVAX agrees that it waives any right to assert, in any context, that adding Mr. Lindvall as a partner of Kaye Scho-ler creates an ethical conflict, including, but not limited to, any right to seek to disqualify Kaye Scholer from serving as counsel of record for Pfizer in the Neu-rontin or Gabapentin Matter or in any of the individual actions included within those matters, or from serving as counsel to Pfizer in connection with any FDA issues relating to Neurontin or gabapen-tin.

(Sherman Decl. Ex. 1) Mr. Rubin accepted the terms of the proposed arrangement and agreed to the waiver. (Id.; Rubin Decl. Ex. A) Mr. Sherman subsequently sent a letter proposing the same waiver for Ms. Clarke, to which Mr. Rubin likewise agreed. (Sherman Decl. Ex.2; Rubin Decl. Ex. B) Neither Mr. Mentlik nor Mr. Rubin consulted or sought approval from the other Firsh-Wave Defendants. (Amundson Decl. ¶ 15; Molino Decl. ¶ 10; Lieberstein Decl. ¶ 12) Furthermore, there is no evidence in the record that Kaye Scholer advised any of the other Firsb-Wave Defendants of its request for a waiver from Ivax or sought any corresponding waiver from them.

Kaye Scholer admits that, at the time of these negotiations, it was aware of the possibility that Pfizer might ask the firm to represent it in the Gabapentin action. (Sherman Decl. ¶ 2) So was Ivax, though Mr. Rubin now contends that when the waivers were executed, he was not informed, nor was it contemplated (presumably he means by Mr. Rubin himself) that Kaye Scholer would later seek to be substituted as lead counsel in this matter for the Fitzpatrick Celia firm. (Rubin Decl. ¶ 7) The terms of the proposed waiver agreement clearly and unambiguously indicate that Kaye Scholer’s participation in the Gabapentin action is contemplated. By agreeing to the waiver, which specifically covers waiving the right to seek to disqualify Kaye Scholer from serving as lead counsel to Pfizer in the Gabapentin matter, Ivax and Mr.

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In Re Gabapentin Patent Litigation, 407 F. Supp. 2d 607, 2005 WL 3597691 (D.N.J. 2005).

407 F. Supp. 2d 607 (In Re Gabapentin Patent Litigation) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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