Genentech, Inc. v. United States International Trade Commission

122 F.3d 1409
CourtCourt of Appeals for the Federal Circuit
DecidedAugust 14, 1997
DocketNo. 95-1244
StatusPublished
Cited by5 cases

This text of 122 F.3d 1409 (Genentech, Inc. v. United States International Trade Commission) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Genentech, Inc. v. United States International Trade Commission, 122 F.3d 1409 (Fed. Cir. 1997).

Opinion

ARCHER, Chief Judge.

Genentech, Inc. (Genentech) appeals the final determination of the United States International Trade Commission (ITC or Commission), Genentech, Inc. v. United States Int’l Trade Comm’n, No. 337-TA-358 (Nov. 29, 1994) (Initial Determination), (Jan. 17, 1995) (Final Determination and Commission Opinion), dismissing Genentech’s amended complaint alleging a violation of § 337 of the Tariff Act of 1930, 19 U.S.C. § 1337 (1994). The Commission dismissed the complaint as a sanction for discovery misconduct which it found had occurred when Genentech failed to disclose and produce certain documents to supplement discovery in the ITC proceeding until ordered to do so. We reverse and remand.

BACKGROUND

On March 16,1993, Genentech filed a complaint with the ITC seeking an investigation [1412]*1412under § 337 based on the alleged infringement of four of its patents1 relating to recombinant production of human growth hormone (hGH), by Bio-Technology General Corp. and Bio-Technology (Israel) Ltd. (collectively BTG) and Novo Nordisk A/S, Novo Nordisk of North America, Inc., Novo Nor-disk Pharmaceuticals, Inc., and Zymogenetics (collectively Novo). On September 21, 1993, the ITC instituted Investigation No. 337-TA-358 to determine whether BTG and Novo were importing into or selling in the United States recombinantly produced hGH made abroad by processes covered by the claims of the four Genentech patents in violation of § 337.

The administrative law judge (ALJ) assigned to the case issued ground rules for the investigation. These rules included, inter alia, Ground Rules 4(ix) and 5(i), which provided in pertinent part:

4. Discovery
* * i|: *
(ix) A duty to timely supplement all discovery responses upon obtaining information rendering a response substantially incomplete or incorrect is hereby imposed by the ALJ pursuant to Commission interim rule 210.30(d)(3).
* * * *
5. Privileged Matter
(i) During the course of discovery, the following procedure, similar to what is set forth in Duplan v. Peering Millikin [sic] Inc., 397 F.Supp. 1146 (D.S.C.1975), should be followed with respect to those documents for which counsel claims attorney-client and/or work product privilege.
(a) When there is no objection to production of a document other than that the document is subject to a claim of privilege, each such withheld document should be separately identified in a privileged document list, by the party claiming the privilege, which privileged document list shall be provided to the requesting party within ten (10) calendar days following the due date of the response to the discovery request requesting production of the document so withheld.
‡ ‡ ‡ *

Commission Interim Rule (CIR) 210.30(d) also provides:

(2) A party is under a duty to seasonably amend a prior response if he obtains information upon the basis of which—
* * * *
(ii) He knows that the response, though correct when made, is no longer true, and the circumstances are such that a failure to amend the response is in substance a knowing concealment.
CIR 210.30(d)(2).

Discovery proceeded and, upon its completion on March 18, 1994, the ALJ conducted an evidentiary hearing April 11-24, 1994, with closing arguments and post-hearing briefs scheduled for June 9 and 10, 1994. Under Commission rules, the ALJ’s initial determination was originally due by July 29, 1994.2

Meanwhile, during this same period, Genentech was involved in a consolidated “multidistrict” patent infringement suit in the U.S. District Court for the Southern District of Indiana with two parties not involved in the ITC investigation, Eli Lilly & Co. and the Regents of the University of California. In [1413]*1413that litigation, Genenteeh sued on fourteen patents, including the four patents at issue here. During the course of discovery in that action, Genenteeh inadvertently produced approximately 21,000 pages of documents bearing “GLP” Bates stamp numbers (the GLP documents), 12,000 pages of which Genenteeh considered privileged under either the attorney-client privilege or attorney work product privilege.3 Genenteeh did not consider the remaining 9,000 pages to be privileged. Within two weeks of the production, Genentech realized its error and filed an emergency motion for the return of the 12,000 pages of documents. On March 22, 1994, the district court denied the motion because the disclosure resulted from inadequate screening procedures. The court ruled that Genentech had, therefore, waived any privilege as to those documents, although no waiver of the subject matter had occurred. In re Recombinant DNA Tech. Patent and Contract Litig., 850 F.Supp. 769 (S.D.Ind.1994).

Genenteeh did not inform the parties to the ITC investigation or the ALJ about the district court’s ruling on the GLP documents. Instead, BTG learned of the court’s ruling around July 8, 1994, after it was published. BTG, joined by Novo, promptly requested production of the GLP documents by Genentech. BTG and Novo claimed entitlement to the GLP documents due to Genentech’s waiver of privilege in the district court litigation.

Genenteeh resisted disclosure in the ITC proceeding of 12,000 pages of the GLP documents it thought should be privileged. It argued that the interlocutory ruling of the district court only affected that proceeding and also that the protective order in that proceeding controlled access to these GLP documents. Because BTG and Novo were not parties to that action, Genenteeh contended that they were not entitled under the protective order to any of the documents. For these reasons, Genenteeh declined to produce voluntarily any of the 12,000 pages of GLP documents that it claimed were privileged.

As to the remaining 9,000 pages of GLP documents, Genenteeh confirmed that of the some 2900 pages that were relevant to the ITC investigation all except 60 had previously been produced. Genenteeh also believed these 60 pages had been produced but had not established that belief. In order to avoid delay, Genenteeh voluntarily produced these remaining pages.

On July 15, 1994, the ALJ ordered Genentech to produce the 12,000 pages of GLP documents, finding that “the documents in issue were found not to be privileged by the [district court] and therefore any privilege has been waived.” Genenteeh promptly complied with the ALJ’s order by producing the 12,000 pages to BTG and Novo on July 19, 1994.

On July 21,1994, BTG and Novo moved to reopen the record to admit additional evidence relating to the GLP documents, to extend the date for the issuance of the initial decision, and for sanctions against Genenteeh. The ALJ denied the motion to reopen the record and the motion for sanctions, explaining that neither BTG nor Novo had identified the materiality of any of the GLP documents or any specific discovery request with which Genenteeh failed to comply.

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Bluebook (online)
122 F.3d 1409, Counsel Stack Legal Research, https://law.counselstack.com/opinion/genentech-inc-v-united-states-international-trade-commission-cafc-1997.