Merck Eprova AG v. ProThera, Inc.

670 F. Supp. 2d 201, 2009 U.S. Dist. LEXIS 126632, 2009 WL 4067209
CourtDistrict Court, S.D. New York
DecidedSeptember 17, 2009
Docket08 Civ. 0035(RMB)(JCF)
StatusPublished
Cited by33 cases

This text of 670 F. Supp. 2d 201 (Merck Eprova AG v. ProThera, Inc.) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Merck Eprova AG v. ProThera, Inc., 670 F. Supp. 2d 201, 2009 U.S. Dist. LEXIS 126632, 2009 WL 4067209 (S.D.N.Y. 2009).

Opinion

MEMORANDUM AND ORDER

JAMES C. FRANCIS IV, United States Magistrate Judge.

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- *204 5-methyl(6S)-pteridinyl)methyl]amino-]benzoyl]-L-glutamic acid, calcium salt. (Compl., ¶ 9). This chemical is otherwise identified as L-5-methyltetrahydrofolic acid, calcium salt (“L-5-MTHF”). (Compl., ¶ 9). L-5-MTHF is a pure diastereoisomeric form of the compound 5-me-thyltetrahydrofolie acid. (Compl., ¶ 9). L-5-MTHF is a source of folate, a vitamin of the B complex, and has been used in pregnancy vitamins, nutritional supplements, and special dietary and medical foods. (Compl., ¶¶ 10,11).

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 *205 shall keep the other Party informed with regard to the patent application and maintenance processes ... and shall promptly deliver to the other Party copies of all patent applications, amendments, related correspondence and other relevant materials.” (Katz Deck, Exh. A at 17).

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.

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670 F. Supp. 2d 201, 2009 U.S. Dist. LEXIS 126632, 2009 WL 4067209, Counsel Stack Legal Research, https://law.counselstack.com/opinion/merck-eprova-ag-v-prothera-inc-nysd-2009.