MEMORANDUM AND ORDER
Plaintiffs Merck KGaA and its Swiss affiliate, Merck Eprova (collectively, “Merck”), allege that defendant ProThera, Inc. (“ProThera”) has mislabeled a nutritional supplement that it distributes. According to Merck, ProThera’s conduct constitutes direct and contributory false advertising in violation of Section 43(a)(1)(B) of the Lanham Act, 15 U.S.C. § 1125(a)(1)(B); contributory trademark infringement in violation of Section 32(1) of the Lanham Act, 15 U.S.C. § 1114(1); trademark dilution in violation of Section 43(c) of the Trademark Dilution Revision Act of 2006 and the Federal Trademark Dilution Act of 1995, 15 U.S.C. § 1125(c); unfair competition in violation of Section 43(a)(1)(A) of the Lanham Act, 15 U.S.C. § 1125(a)(1)(A); unfair competition in violation of New York common law; trademark dilution in violation of Section 360-1 of the New York General Business Law; deceptive trade practice in violation of Section 349(h) of the New York General Business Law; and false advertising in violation of Sections 350 and 350-e(3) of the New York General Business Law. (Complaint (“Compl.”), ¶ 1).
Merck now moves to disqualify one of ProThera’s counsel, the firm of Frommer Lawrence & Haug LLP (“FLH”), on the ground that this firm has been representing Merck in a related patent prosecution at the same time that it has been litigating against Merck here. Merck further contends that FLH must be disqualified because Dr. Howard Rosenberg, an in-house scientific advisor for FLH, previously worked for Merck and provided advice in connection with the same chemical compound that is at issue here. ProThera opposes the motion, arguing that Merck is not a client of FLH in the patent matter, that the patent prosecution is not substantially related to this case, that disqualification would prejudice ProThera, and that Dr. Rosenberg’s relationship with Merck does not warrant disqualification. Furthermore, ProThera contends that because FLH is no longer representing any party in the patent matter, any basis for disqualification has evaporated.
For the reasons that follow, Merck’s motion is granted.
Background
A. The Current Litigation
Merck markets a dietary supplement using trademarks that incorporate the term “Metafolin.” (Compl., ¶¶ 8-11). The Metafolin marks are used by Merck in connection with the dietary ingredient N-[4- [¶] (2-amino-5,6,7,8-tetrahydro-4-hydroxy-
The chemical 5-MTHF is a mixture of two diastereoisomers, the “L-form” and the “D-form.” (Compl., ¶ 20). The L-form is a naturally occurring form of folate found in food and in the human body and is biologically active, while the D-form is not present in nature and cannot be metabolized in the body. (Compl., ¶ 21). According to Merck, the presence of the D-form could reduce the effectiveness of a folate supplement by competing with the uptake and activity of the beneficial L-form. (Compl., ¶ 23).
Beginning in 2005, Merck supplied L-5MTHF to ProThera and allowed ProThera to use the Metafolin trademarks pursuant to a license agreement. (Compl., ¶ 36). However, Merck terminated the license in August 2006, allowing ProThera to deplete its inventory over the following month. (Compl., ¶¶ 37-39). Nevertheless, Merck determined that ProThera and some of its distributors were still using the Metafolin marks in 2007. (Compl., ¶ 40). Furthermore, Merck tested products manufactured or distributed by ProThera and discovered that although they were labeled or advertised as containing L-5-MTHF, in fact they contained the diastereoisomeric mixture 5-MTHF (i.e., they contained both the L-form and the D-form). (Compl., ¶ 40).
Merck commenced the instant litigation in January 2008. From the inception of the case, ProThera has been represented by Joshua King of Graybeal Jackson LLP and by local counsel, James N. Blair of Snow Becker Krauss P.C. In November 2008, Gregory Wilson of Wilson & Quint LLP joined as co-counsel. Then, on February 6, 2009, Charles Raubicheck of FLH filed his appearance as additional co-counsel.
B. The Patent Proceedings
On August 1, 2005, Merck Eprova entered into an exclusive license agreement (the “Agreement”) with Schering AG, which later became Bayer Schering Pharma AG (“Bayer”). (Declaration of Vera A. Katz dated June 5, 2009 (“Katz Deck”), ¶ 3 & Exh. A). The purpose of the Agreement was to facilitate joint development of new pharmaceutical products that include L-5-MTHF. (Katz Deck, ¶4). In that connection, the Agreement made provision for prosecution of a joint patent:
[Bayer] shall direct and control the preparation, filing and prosecution of the patent applications with respect to the Joint Patent (including any interferences and foreign oppositions) in the name of [Merck Eprova] and [Bayer].... [Merck Eprova] shall provide to [Bayer] appropriate powers of attorney to enable [Bayer] to act on behalf of [Merck Eprova] before the patent authorities with respect to the Joint Patent.... In the event that [Bayer] declines or fails to file any patent application with respect to the Joint Patent in the Territory, or intends to abandon all patent applications without filing a continuation of such patent applications, [Bayer] shall provide [Merck Eprova] a reasonable opportunity to file and/or to prosecute such patent application on [Merck Eprova’s] behalf.
(Katz Deck, Exh. A at 17). The Agreement further provides that “[e]ach Party
Pursuant to the Agreement, Merck Eprova and Bayer filed two joint patent applications, U.S. Patent Application Nos. 11/435,198 and 11/938,688. (Declaration of Rudolf Moser dated June 5, 2009 (“Moser Deck”), ¶ 4 & Exh. A). The claimed inventions relate to pharmaceuticals that combine estrogens or progestogens with L-5MTHF for use as an oral contraceptive. For purposes of prosecuting these pending patent applications, Bayer engaged Thomas J. Kowalski of FLH, which had long represented it in patent matters, including patents over which the current applications claim priority. (Declaration of Thomas J. Kowalski dated June 18, 2009 (“Kowalski Deck”), ¶¶ 4-5, 8-9).
According to FLH, it represented Bayer exclusively in connection with the pending applications. FLH received compensation only from Bayer and not from Merck. (Kowalski Deck, ¶¶ 3, 30-31). It took direction only from Bayer and not from Merck. (Kowalski Deck, ¶ 40). And, it communicated only with Bayer and not with Merck. (Kowalski Deck, ¶¶ 3, 29, 31, 46).
Merck Eprova, on the other hand, always understood that FLH represented it as well as Bayer in connection with the pending applications. (Katz Deck, ¶ 10). Because of their joint interest, Merck communicates with Bayer regarding any patent applications arising from the Agreement, “discussing, for instance, communications they have received from patent attorneys in different countries where the applications have been filed.” (Katz Deck, ¶ 12). One of the inventors identified in the pending applications, Dr. Rudolf Moser, is a Merck employee from whom FLH obtained a power of attorney in connection with the applications. (Mos-er Deck, ¶¶ 1, 3, 8-9 & Exh. B). Dr. Moser also executed an assignment of his rights in the invention to Merck and Bayer jointly. (Moser Deck, ¶ 10 & Exh. C).
Bayer, too, believed that FLH represented Merck. When Bayer became aware of the current dispute, it sent a letter to FLH that states in part:
As you know, Merck Eprova was coassignee when we filed the ... patent applications and still is today____ We were surprised to hear that you do not consider Merck Eprova as your client. We are no experts in U.S. patent law, but in the European system, in such a case, the representative of one patent owner would automatically be the representative of all patent owners. When we communicated with you about these applications, it was on behalf of both us and Merck Eprova.
(Letter from Uwe Hartmann and Andreas Brosamle to Thomas Kowalski dated June 26, 2009 (“Hartmann Letter”), attached as Exh. A to Declaration of Andreas Furger dated June 26, 2009 (“Furger Deck”), at 1).
Bayer expressed concern about the relationship between the patent applications and the instant litigation. It told FLH that “Merck Eprova informed us that the subject matter of their litigation against Prothera [sic] is not a pure trademark matter but the question of which substance can be labelled [sic] as L-5-MTHF. Metafolin (L-5-MTHF) is an essential part of the inventions claimed in our patent applications.” (Hartmann Letter at 1). This anxiety led Bayer to terminate FLH as counsel on the patent applications:
We are concerned that subject matter discussed in the Prothera [sic] case is related to the ... patent applications and may be adverse to them. We arenot a party to this litigation and have no interest in being involved in it. Our sole interest here is to safeguard our IP rights. Therefore, we decided to transfer the ... patent applications to another law firm. Merck Eprova agreed to that transfer. Please stop working on these applications and wait for our transfer instruction which we will send to you soon.
(Hartmann Letter at 2).
C. The Role of Dr. Rosenberg
Dr. Rosenberg holds a Ph.D. degree in pharmacology. (Declaration of Howard E. Rosenberg dated June 11, 2009 (“Rosenberg Deck”), ¶ 2). From 1986 through 2008, he was employed by Generics (UK) Ltd., a member of the Merck Generics Group, which in turn was a subsidiary of Merck KGaA. (Rosenberg Deck, ¶ 3). According to Dr. Rosenberg, his “work focused on research and development of generic pharmaceuticals, and the intellectual property landscape surrounding generic products.” (Rosenberg Deck, ¶ 3). In that capacity, he “was involved in aspects of chemical synthesis, development, and patentability of active ingredients used in generic pharmaceutical products.” (Rosenberg Deck, ¶ 3). Dr. Rosenberg characterizes his involvement with L-5MTHF as limited:
While at Merck Generics, I had a few occasional discussions with Dr. Martin Ulmann, an employee of Merck Eprova AG (another subsidiary of Merck KGaA) concerning the folate compound L-5MTHF. Dr. Ulmann was directing a project seeking to develop this compound for commercial purposes.... At his request, I commented to Dr. Ulmann about the possibility of obtaining patents for L-5-MTHF. I did not draft any claims in an patent application for this compound. I was not an inventor named in any patent applications. I had no decision-making responsibility nor any role in filing patent applications for this compound.
(Rosenberg Deck, ¶¶ 4-5).
Merck views Dr. Rosenberg’s role in connection with L-5-MTHF as more extensive:
During his tenure at Merck, Dr. Rosenberg assisted in the development of Merck’s intellectual property strategies, including Merck Eprova’s strategies for L-5-MTHF. In fact, as part of this strategic planning, Dr. Rosenberg visited Merck Eprova’s L-5-MTHF plant in Switzerland and, on more than one occasion, consulted with Merck Eprova regarding the [intellectual property] protection strategy for L-5-MTHF in the United States and elsewhere. This involvement included Dr. Rosenberg’s assisting in the drafting of claims for patent applications related to L-5-MTHF. Dr. Rosenberg also engaged in many conversations with Merck Eprova’s managing director, Martin Ulmann, relating to possible protection strategies for Merck’s L-5-MTHF product.
(Katz Deck, ¶ 17). In support of its characterization, Merck points to an e-mail that Dr. Rosenberg sent in response to a notice of a meeting that he attended concerning amendments to patent claims for L-5MTHF. (Furger Deck, ¶¶ 7-9). In that e-mail. Dr. Rosenberg indicated that he had reviewed the patent application and had questions concerning the forms of the compound and about whether Merck wished to claim each form separately. He stated that he would prefer to “talk it through” in the face-to-face meeting and discuss Merck’s objective and what it intended to protect. (Furger Deck, Exh. B).
In January 2009, Dr. Rosenberg was hired as a scientific advisor for FLH. (Rosenberg Deck, ¶ 1). Since that time, he has had no substantive involvement with any matter concerning L-5-MTHF, in-
Discussion
A. Principles of Disqualification
Motions to disqualify counsel are viewed with disfavor and subjected to a high standard of proof, in large part because they can be used as a litigation tactic.
See Evans v. Artek Systems Corp.,
The authority to disqualify an attorney is a function of the court’s inherent supervisory power.
See id.; Medical Diagnostic Imaging,
Disqualification is warranted where an attorney’s conduct tends to taint the underlying proceedings.
See Hempstead Video,
a lawyer shall not represent a client if a reasonable lawyer would conclude that either:
(1) the representation will involve the lawyer in representing differing interests; or
(2) there is a significant risk that the lawyer’s professional judgment on behalf of a client will be adversely affected by the lawyer’s own financial, business, property or other personal interests.
Rule 1.7(a). 2 The second relevant ethical requirement is that an attorney maintain client confidences. This obligation is contained in Rule 1.6, which states in part that “A lawyer shall not knowingly reveal confidential information ... or use such information to the disadvantage of a client or for the advantage of the lawyer or a third person[.]” Rule 1.6(a). 3
Where a conflict is alleged, “[t]he standard for disqualification varies depending on whether the representation is concurrent or successive.”
Hempstead Video,
In a case of successive representation, an attorney may be disqualified where:
(1) the moving party is a former client of the adverse party’s counsel;
(2) there is a substantial relationship between the subject matter of the counsel’s prior representation of the moving party and the issues in the present lawsuit; and
(3) the attorney whose disqualification is sought had access to, or was likely to have had access to, relevant privileged information in the course of his prior representation of the client.
Id.
(quoting
Evans,
As noted above, FLH’s responsibility for the patent applications was terminated when Bayer transferred that assignment to other counsel on June 26, 2009. (Furger Decl., Exh. A). According to ProThera, this “makes it crystal clear that the basis for Merck’s motion has vanished. Assuming solely for argument’s sake that Merck had an attorney-client relationship with FLH, it has now gone with the transfer.” (ProThera’s Sur-Reply Memorandum Opposing Merck’s Motion to Disqualify Frommer Lawrence & Haug LLP as its Counsel (“ProThera Sur-Reply”) at 6). However, if there had been an attorney-client relationship between Merck and FLH, the termination of that relationship would not end the disqualification inquiry altogether. At the very least, the potential conflict would have to be analyzed under the standards for successive representation.
And, indeed, where counsel have simultaneously represented clients with differing interests, the standard for concurrent representation applies even if the representation ceases prior to the filing of a disqualification motion.
Unified Sewerage Agency of Washington County, Oregon v. Jelco Inc.,
ProThera seems to suggest that such reasoning does not apply here because, rather than seeking to withdraw from representing Merck, FLH was terminated. (ProThera Sur-Reply at 6 n. 4). But the rule requiring a conflict to be judged by the concurrent representation standard even after representation has ended should not turn on whether representation is terminated by conflicted counsel or by the client. Otherwise, counsel could simply persist in dual representation until one client or the other capitulates. Counsel should not be rewarded for delaying resolution of a conflict issue by being accorded a less demanding disqualification standard. Accordingly, the higher standard for concurrent representation applies in this case.
The appropriate standard of analysis depends not only on whether the representation is concurrent or successive, but also on the quality of the attorney-client relationship. A strict standard “is properly imposed when a lawyer undertakes to represent two adverse parties, both of which are his clients in the traditional sense.”
Glueck v. Jonathan Logan, Inc.,
“The formation of an attorney-client relationship hinges upon the client’s [reasonable] belief that he is consulting a lawyer in that capacity and his manifested intention to seek professional legal advice.”
Diversified Group, Inc. v. Daugerdas,
1) whether a fee arrangement was entered into or a fee paid; 2) whether a written contract or retainer agreement exists indicating that the attorney accepted representation; 3) whether there was an informal relationship whereby the attorney performed legal services gratuitously; 4) whether the attorney actually represented the individual in one aspect of the matter (e.g., at a deposition); 5) whether the attorney excluded the individual from some aspect of [the] litigation in order to protect another (or a) client’s interest; 6) whether the purported client believes that the attorney was representing him and whether this belief is reasonable.
Medical Diagnostic Imaging,
But ProThera’s argument fails to take into account how this test must be construed in the context of joint representation.
See In re Regents of University of California,
Likewise, where two parties are jointly prosecuting a patent application, they are commonly considered to be joint clients.
See Beasley v. Avery Dennison Corp.,
No. SA-04-CA-0866,
Courts have long recognized the existence of the attorney-client relationship among clients and attorneys allied in a common legal cause. Typically, parties jointly developing a patent with an attorney commonly have a “common legal interest” in obtaining the greatest protection and in exploiting the patents. The parties thereby develop a “community of interest,” which establishes a joint attorney-client relationship among them and the attorney. In this respect, when a community of interest exists, courts have viewed those represented as “joint clients” for the purpose of privilege.
Hillerich & Bradsby,
Here, there is no dispute that Bayer and Merck intended to file joint patent applications and that Bayer engaged FLH to prosecute those applications. It was therefore reasonable for
The cases cited by ProThera do not undermine the conclusion that there was joint representation. In both
Sun Studs,
Bayer and Merck, then, were both clients of FLH “in the traditional sense.”
Chemical Bank,
3. Potential Taint
The gravamen of Merck’s complaint in this case is that ProThera mislabels its product as L-5-MTHF when, in fact, it is the diastereoisomeric mixture, 5-MTHF, and therefore unfairly competes with Merck’s Metafolin product, which is “pure” L-5-MTHF. Accordingly, even though this is an unfair competition case, the therapeutic characteristics of these compounds are central to the claims. The uniqueness of L-5-MTHF is an important element of Merck’s argument that its product and ProThera’s are distinct in material ways and that ProThera’s labeling is therefore misleading. So too, the unique properties of L-5-MTHF are critical to the patent applications. Its characteristics are plainly relevant to the patent claims asserted and the ultimate patentability of the drugs for which Merck and Bayer seek patent protection.
This highlights the conflicted position in which FLH finds itself. On one hand, in the patent prosecution, it is in the interest of Merck (as represented by FLH) to establish that only L-5-MTHF can serve certain therapeutic purposes. On the other hand, in this litigation, ProThera (also
The close relationship between the patent prosecution and this case has two significant legal consequences. First, ProThera cannot establish the necessary predicate for escaping disqualification under the per se rule. Second, even if the per se rule did not apply because FLH’s representation of Merck is considered merely indirect or attenuated, disqualification would still be appropriate because of the substantial nexus between the matters in which FLH represents adverse interests.
See British Airways,
4. Remaining Considerations
In the absence of a direct conflict of interest, courts may exercise discretion in determining whether to disqualify counsel on the basis of a violation of ethical principles.
See Purgess v. Sharrock,
a. Tactical Advantage
ProThera argues that Merck’s motion should be denied because it was interposed for tactical reasons, as demonstrated by the timing of the motion and the absence of any taint arising from the dual representation. (Def. Memo, at 18-20). Merck’s motion was indeed somewhat delayed. Based on the imputed knowledge of its counsel, Merck learned on February 6, 2009 that FLH was representing ProThera in this case. And, of course, Merck knew at that time that FLH was also representing it in the patent applications. Yet, it did not advise FLH of its intention to file the instant motion until May 8, 2009.
There is, however, an entirely reasonable explanation for this delay. While Merck’s counsel immediately became aware of FLH’s representation of ProThera, that counsel had no reason to know that FLH was simultaneously representing Merck in the patent proceedings. (Furger Deck, ¶ 13). On the other hand, business executives at Merck knew that FLH was prosecuting the patents but did not realize that FLH had undertaken representation of ProThera. (Furger Deck, ¶ 13). Only when an attorney for Merck in this proceeding discovered that FLH had listed Merck as a client on its website, did counsel engage in the research necessary to identify the conflict. (Declaration of Robert E. Hanlon dated June 5, 2009, ¶¶ 7-8). The delay, then, is not indicative of sharp tactics.
Likewise, tactical motivations cannot be inferred from an absence of taint in the proceedings thus far. As discussed above, the significant relationship between the patent applications and this litigation make it likely that dual representation would indeed taint these proceedings.
b. Prejudice
ProThera will, of course, suffer some additional cost and delay if FLH is disqualified. Certain factors, however, mitigate that prejudice. First, FLH only recently appeared in this case; this is not a situation where counsel who have been the exclusive attorneys throughout a litigation are disqualified on the eve of trial. Second, while ProThera expresses concern
Thus, even if these considerations are properly addressed in a case of a direct conflict, they do not overcome the factors favoring disqualification in this instance.
C. Status of Dr. Rosenberg
In view of the fact that disqualification is warranted on the basis of dual representation by FLH, there is no need to address Dr. Rosenberg’s status as a scientific ad-visor for FLH.
Conclusion
For the reasons set forth above, Merck’s motion is granted, and FLH is relieved as counsel for ProThera.
SO ORDERED.
Notes
. Previously, lawyers in New York were subject to the New York Code of Professional Responsibility and its Disciplinary Rules (the "Old Rules”), which were based in turn on the American Bar Association Model Code of Professional Responsibility (the “Model Code”). In 1983, the ABA replaced its Model Code with the Model Rules, but New York did not immediately adopt the Model Rules. Instead, New York retained the Old Rules until April 1, 2009, when it replaced them with the New York Rules of Professional Conduct (the "New Rules”). N.Y. Comp.Codes R. & Regs, tit. 22, § 1200
et seq.
(2009);
see Leslie Dick,
. This rule is substantively similar to Canon 5, Disciplinary Rule ("DR”) 5-105(A)-(B), and DR 5-101 of the Old Rules.
. This is analogous to Canon 4 and DR 4-101 of the Old Rules.
. Unfortunately, joint representation is frequently confused with the "common interest" doctrine, also known as the "joint defense” doctrine.
See Jordan (Bermuda) Investment Co.,
. Provision of the power of attorney did not, by itself, create any attorney-client relationship between Merck and FLH.
See Sun Studs, Inc. v. Applied Theory Associates, Inc.,
