Ciba-Geigy Corp. v. Alza Corp.

795 F. Supp. 711, 23 U.S.P.Q. 2d (BNA) 1932, 1992 U.S. Dist. LEXIS 8635, 1992 WL 119927
CourtDistrict Court, D. New Jersey
DecidedJune 5, 1992
DocketCiv. A. 91-5286
StatusPublished
Cited by8 cases

This text of 795 F. Supp. 711 (Ciba-Geigy Corp. v. Alza Corp.) is published on Counsel Stack Legal Research, covering District Court, D. New Jersey primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Ciba-Geigy Corp. v. Alza Corp., 795 F. Supp. 711, 23 U.S.P.Q. 2d (BNA) 1932, 1992 U.S. Dist. LEXIS 8635, 1992 WL 119927 (D.N.J. 1992).

Opinion

OPINION

WOLIN, District Judge.

Before the Court is the motion by defendants, Alza Corporation (“Alza”) and Marion Merrell Dow (“Marion”) (collectively “defendants”), to disqualify plaintiffs counsel, pursuant to New Jersey Rules of Professional Conduct (“R.P.C.”) 1.9(a)(1), 1.9(a)(2) or 1.9(b). For the reasons expressed below, this Court will deny defendants’ motion.

I. BACKGROUND

Plaintiff, Ciba-Geigy Corporation (“Ciba-Geigy”), who is represented by Kenyon & Kenyon, commenced an action against defendants for patent infringement (the “NICODERM litigation”). In particular, Ciba-Geigy claims that defendants’ NI-CODERM product infringes Ciba-Geigy’s 5,016,652 patent (the “ '652 patent”). Ciba-Geigy produces HABITROL under its '652 patent.

The '652 patent covers a transdermal delivery system for nicotine. According to the patent, a transdermal patch is adhered to a person’s skin. The device delivers nicotine into the person’s body through the skin. According to Ciba-Geigy, the Habi-tad patch, manufactured in accordance with the ' 652 patent, helps people to cease smoking because it weans them from their physical addiction to nicotine.

Defendants move to disqualify Kenyon & Kenyon because of their prior representation of Alza and Ciba-Geigy in a patent infringement action (the “PACO litigation”), involving the transdermal delivery of estradiol into the body. As opposed to nicotine, which is a porous substance and therefore can be injected directly into the body, estradiol is a non-porous substance. Because of its non-porous nature, in contrast to nicotine, estradiol is delivered through the skin using ethanol as an enhancer.

In the prior litigation Ciba-Geigy and Alza sued PACO for infringing Alza’s 3,948,262 patent (the “ '262 patent”), 4,144,-317 patent, (the “ '317 patent”), and 4,370,-454 patent (the “ '454 patent!’). 1 Alza and Ciba-Geigy marketed ESTRADERM, an es-tradiol transdermal patch, Under these patents.

In connection with the PACO litigation, Kenyon & Kenyon responded to PACO’s document request. As Ciba-Geigy correctly indicates, PACO’s document request extended beyond documents that concerned the '454 patent and the transdermal delivery of estradiol. Kenyon & Kenyon objected to the broad request, and only produced documents limited to estradiol and the '454 patent. Defendants do not dispute Kenyon & Kenyon’s contention. Instead, defendants contend that in order to produce doc: uments solely related to estradiol and the '454 patent, the Kenyon & Kenyon attorneys had to cull through documents that *713 concerned other types of transdermal delivery systems.

Kenyon & Kenyon sent Gail Kempler to collect information responsive to PACO’s document request. Ms. Kempler avers that she only searched through documents culled by Alza employees that related to estradiol or ESTRADERM. Moreover, Ms. Kempler contends that Pat Campbell, an Alza employee who is co-author of the NI-CODERM patent and the ESTRADERM patent, only produced documents that related to estradiol and ESTRADERM. In particular, according to Ms. Kempler, Ms. Campbell produced her notebooks related to the ESTRADERM project. In fact, Ms. Kempler recalls that she only conversed with Ms. Campbell about the ESTRA-DERM product and the transdermal delivery of estradiol. Moreover, Ms. Kempler distinctly remembers that “[she] never spoke to anyone at Alza concerning nicotine technology. [Rather] all of [her] conversations were limited to Estraderm and/or estradiol transdermal products.”

Ms. Campbell agrees that she initially produced documents that only related to the ESTRADERM project. She further contends, however, that she subsequently produced documents that related to any of Alza’s transdermal delivery system. Unfortunately, Ms. Campbell does not specify the other transdermal delivery systems for which she supplied documents to Ms. Kem-pler. 2 At the time of the document request, Ms. Campbell did not participate directly in the NICODERM project. By her own admission she was an indirect participant.

As part of the discovery in the PACO litigation, the attorneys who represented PACO deposed Dr. David Enscore, a named inventor of the patent underlying NICO-DERM. Dr. Enscore tested PACO patches and determined that they were “inoperative and did not provide the release of estradiol through the skin in therapeutic amounts.” PACO’s attorneys limited Dr. Enscore’s deposition to the manner in which he tested the PACO product. PACO’s attorneys requested documents relating to Dr. Ens-core’s testing of the PACO product.

Robert A. Fier, Esq., Steven J. Lee, Esq., and Hugh A. Chapin, Esq. prepared Dr. Enscore for his deposition. As part of the preparation, Dr. Enscore provided these Kenyon & Kenyon attorneys “with Alza’s Analytical Research Test Method for testing release rates of ethanol and estradiol as well as test methods for measuring trans-dermal flux of the system, and the analytical data backing up his analysis.” In accordance with the Notice of Oral Deposition under Fed.R.Civ.P. 30(b)(6), Kenyon & Kenyon’s attorneys turned over the testing methods used by Dr. Enscore to PACO’s lawyers. Mr. Lee was primary counsel at Dr. Enscore’s deposition. Mr. Chapin also was present at the deposition.

Both Mr. Fier and Mr. Lee averred that their discussions with Dr. Enscore only concerned his testing of the PACO estra-diol patches and did not cover any other type of chemical transdermal device. Dr. Enscore contraverts these averred statements and asserts that he discussed trans-dermal delivery systems with the Kenyon & Kenyon lawyers. Dr. Enscore never discloses which other systems he discussed with the Kenyon & Kenyon attorneys. Instead, he only specifies that he disclosed his testing of the PACO estradiol patch.

II. DISCUSSION

Defendants assert three reasons that compel this Court to disqualify Kenyon & Kenyon from its representation of plaintiff in the present action, because of its prior representation of Alza. First, defendants allege that R.P.C. 1.9(a)(1) mandates that this Court disqualify Kenyon & Kenyon because the PACO litigation is substantially related to the Nicoderm action. 3 Specifically, defendants contend that both the ES- *714 TRADERM and NICODERM systems are tested in a similar manner, both systems use similar rate control membranes and the control of the agent (ethanol and nicotine respectively) is similar since both are volatile and both systems utilize non-porous membranes. Enscore Declaration In Support of Motion to Disqualify Plaintiff’s Counsel (“Enscore Declaration”) ¶ 8.

Secondly, defendants argue that Kenyon & Kenyon must be disqualified because in the present litigation Kenyon & Kenyon necessarily will use information obtained in the prior litigation and thus will violate R.P.C. 1.9(a)(2). 4 Alza provided Kenyon & Kenyon with information concerning its testing of the infringing PACO product as compared to the ESTRADERM product.

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795 F. Supp. 711, 23 U.S.P.Q. 2d (BNA) 1932, 1992 U.S. Dist. LEXIS 8635, 1992 WL 119927, Counsel Stack Legal Research, https://law.counselstack.com/opinion/ciba-geigy-corp-v-alza-corp-njd-1992.