Chiron Corp. v. Genentech, Inc.

179 F. Supp. 2d 1182, 2001 U.S. Dist. LEXIS 22408, 2001 WL 1700414
CourtDistrict Court, E.D. California
DecidedDecember 10, 2001
DocketCIV S-00-1252WBSGGH
StatusPublished
Cited by14 cases

This text of 179 F. Supp. 2d 1182 (Chiron Corp. v. Genentech, Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. California primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Chiron Corp. v. Genentech, Inc., 179 F. Supp. 2d 1182, 2001 U.S. Dist. LEXIS 22408, 2001 WL 1700414 (E.D. Cal. 2001).

Opinion

ORDER

HOLLOWS, United States Magistrate Judge.

On December 6, 2001, the parties, by and through their counsel, were heard in connection with Chiron’s motion to compel further production of documents related to the advice of counsel defense asserted by Genentech. Counsels’ appearances were identified on the record.

Introduction and Summary

One of the defenses raised in the instant litigation (hereafter the ’561 patent) 1 is advice of counsel. This defense pertains to Chiron’s claim that Genentech willfully infringed the ’561 patent. Genentech agrees that it has waived attorney-client privilege and work product immunity because of its affirmative defense; the issue disputed is the scope or extent of the waiver. Subsidiary disputes involve the completeness of Genentech’s privilege log; however, these disputes will be resolved (to a large extent) by the court’s specific rulings on the extent of Genentech’s waiver.

After thorough consideration of the parties’ positions, and in light of the analysis below, the court finds that Genentech shall produce (to the extent that it has not already done so):

1. All documents reflecting communications, including those otherwise encompassed by the attorney-client privilege, to and from Knobbe regarding the infringement/validity analysis of the ’561 patent (September 2000 letter), up through and including the present time;

2. All documents reflecting communications to and from Knobbe regarding the infringement/validity analysis of the ’894 patent (December 1998 letter) up through and including the present time;

3. All documents reflecting communications to and from the Lyon law firm on the subject of the advice given in the Lyon letter referenced in the ’894 patent letter discussion up through and including the present time;

4. All documents which Genentech presented, forwarded, or caused to be given to its advice attorneys Knobbe and Lyon for the purpose of acquiring an opinion whether Genentech infringed the ’561 patent, the ’894 patent, and the patent(s) pertinent to the Lyon letter, or whether the ’561 patent, et. ah, was valid;

5. (To the extent not already produced in accordance with paragraph 4 above) all documents relied upon by Knobbe and Lyon and disclosed to Genentech in performing the three referenced infringe-meni/validity analyses (the communicated work product);

6. (To the extent not already produced in accordance with paragraph 4) all documents which Knobbe and Lyon otherwise *1184 reviewed in performing the three referenced infringement/validity analysis which Knobbe and Lyon did not disclose to Gen-entech (the uncommunicated work product);

7. All Genentech privileged documents in the actual or constructive possession of Genentech which expressly refer to the three infringement/validity analyses referenced above, to the extent not produced in accordance with the above paragraphs, up through the present time, regardless of whether those documents would otherwise be encompassed by the attorney-client privilege or work product immunity; Gen-entech shall also produce those attorney-client communication or work product documents within Genentech files, which expressly indicate 2 an opinion or conclusion pertinent to the infringemeni/validity of the ’561 or ’894 patents; the documents to be produced include those based in whole or in part on the Drebin, Greene work referenced in the September 2000 advice letter, or based in whole or in part on the Carter publication and Hudziak patent (’171); the documents to be produced include any University of Pennsylvania licensing documents 3 which expressly indicate an opinion or conclusion pertinent to the infringemeni/validity of the ’561 or ’894 patents.

Genentech need not produce as part of its advice of counsel disclosure:

,1. Documents related to other of Gen-entech’s, Chiron’s, or third party patents, but only to the extent not encompassed by production paragraphs 1-7 above;

2. Any communications or work product created by Genentech’s present litigation counsel of record in this action, despite their being encompassed by the production paragraphs above, as Chiron expressly disclaimed at hearing any request for documents from counsel of record.

Genentech need not further publish a privilege log pertinent to the advice of counsel defense. Moreover, the court declines at this time to perform a document by document review of presently withheld materials (see exhibits attached to joint statement). The court’s directions have been specific enough to obviate such a discussion. If particular documents remain at issue despite these directives, the number of such disputes should be few and manageable for a later motion.

Facts

On September 28, 2000, the law firm of Knobbe, Martens, Olson & Bear sent an opinion letter (authored by Ned A. Israel-sen) to Genentech advising that, in its opinion, Chiron’s ’561 patent was invalid. Knobbe also opined that “Genentech’s Herceptin antibody, as disclosed to us, does not infringe any of claims 1-31 of the 561 patent.” Exhibit 5 at p. 2. Fifty-two pages of complex analysis followed setting forth support for the general opinion rendered in the first two pages of the letter. The present motion does not require a detailed discussion of the analysis. However, the analysis referenced in part a prior, and similarly lengthy, opinion letter *1185 issued by Knobbe concerning Genentech’s potential for infringement of the ’894 patent. That opinion letter related that Chi-ron’s ’894 patent was invalid for various reasons, and that “Genentech’s humanized pl85 HER2 antibody does not infringe any of the claims of the ’894 patent.” Exhibit 5 (December 14, 1998 letter) at p. 5. The December 14, 1998 opinion letter also reviewed and relied upon a prior opinion letter issued by the law firm of Lyon & Lyon. Id. at p. 1.

Genentech advanced an advice of counsel defense in the ’561 case. Chiron claims that Genentech thereby waived privilege and work product immunity not only with respect to the letters themselves, but also including a multitude of related documents. Categorically, Chiron seeks all documents “that are directly related to the Knobbe opinions,” “that relate to other legal advice it received on the subject matter addressed in the Knobbe opinions,” including those documents related to Gen-entech’s prosecution of the Drebin/Greene Application and “its prosecution of a series of Genentech patents relating to Hercep-tin.”

Genentech takes a much narrower view of the scope of waiver occasioned by assertion of the advice of counsel defense. Aside from copies of the opinions themselves, it asserts that “all materials actually communicated to it from [Knobbe] that pertain to the relevant subject matter, and all internal [Genentech] documents referring to the 2000 Opinion or analyzing the ’561 patent,” are the total of documents required to be produced to Chiron as a result of the purposeful waiver. Discussion

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Cite This Page — Counsel Stack

Bluebook (online)
179 F. Supp. 2d 1182, 2001 U.S. Dist. LEXIS 22408, 2001 WL 1700414, Counsel Stack Legal Research, https://law.counselstack.com/opinion/chiron-corp-v-genentech-inc-caed-2001.