Sanofi-Aventis v. BARR LABORATORIES, INC.

598 F. Supp. 2d 632, 2009 U.S. Dist. LEXIS 13109, 2009 WL 427518
CourtDistrict Court, D. New Jersey
DecidedFebruary 20, 2009
DocketCivil Action 07-1605 (WJM)
StatusPublished
Cited by4 cases

This text of 598 F. Supp. 2d 632 (Sanofi-Aventis v. BARR LABORATORIES, INC.) 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
Sanofi-Aventis v. BARR LABORATORIES, INC., 598 F. Supp. 2d 632, 2009 U.S. Dist. LEXIS 13109, 2009 WL 427518 (D.N.J. 2009).

Opinion

OPINION

MARK FALK, United States Magistrate Judge.

This matter comes before the Court by way of Defendants’ request for leave to submit a reply expert report limited to the issue of secondary considerations of non-obviousness raised by Plaintiff in its rebuttal expert report on invalidity. The Court has considered the parties submissions on the matter, namely Defendants’ letter dated December 23, 2008 and Plaintiffs letter dated January 14, 2009. 1 No oral argument was heard. Fed.R.Civ.P. 78. For the reasons that follow, Defendants’ request is denied without prejudice.

BACKGROUND

A. The '531 Patent — Ambien CR®

Sanofi-Aventis, Sanofi-Aventis U.S., LLC (“Sanofi-Aventis” or “Plaintiff’) is the owner of Untied States Patent No. 6,514,531 (“the '531 patent”). The '531 patent discloses a pharmaceutical controlled-release dosage form adapted to release Zolpidem or a salt thereof over a predetermined time period. Ambien CR® is an embodiment of the '531 patent. Ambien CR® was approved by the Food and Drug Administration (“FDA”) on September 2, 2005 for the treatment of insomnia.

B. Defendants Seek FDA Approval for Generic Version of Ambien CR®

Defendants, Barr Laboratories, Inc., Mutual Pharmaceutical Co., and Sandoz, Inc. (“Defendants”) each respectively filed an Abbreviated New Drug Application (“ANDA”) pursuant to the Hatch-Waxman Act 2 seeking FDA approval to sell a generic version of the Zolpidem extended-release tablets prior to the expiration of the '531 patent. Each ANDA contains a paragraph IV certification. By filing a paragraph IV certification, Defendants have each taken the position that its generic drug does not infringe the '531 patent or, in the alternative, that the '531 patent is otherwise invalid. See 21 U.S.C. § 355(j)(2)(A)(vn)(IV).

*634 C. Sanofi-Aventis Sues Defendants for Infringement of the '531 Patent

Sanofi-Aventis responded by filing complaints against each Defendant. 3 This invoked an automatic stay under the HatchWaxman Act which prohibits the FDA from approving the generic until the earlier of: (a) the date on which the '531 patent expires, (b) the date on which the Court enters judgment in the infringement lawsuit, or (c) thirty months from the date on which Plaintiff first received notice of Defendants’ respective ANDA paragraph IV filings. See 21 U.S.C. § 355(j)(5XB)(iii); Allergan, 324 F.3d at 1327. 4

D. Expert Discovery

Expert discovery is scheduled to remain open through August 17, 2009. The Court has directed that all expert reports for the issues on which a party bears the burden of proof are due on April 15, 2009 and that all rebuttal expert reports are due on June 17, 2009. See CM/ECF Docket Entry No. 32. By way of letter to the Court dated December 23, 2008, Defendants request leave to submit a reply expert report on secondary considerations of non-obviousness. The Court now considers Defendants’ request.

LEGAL STANDARD

Federal Rule of Civil Procedure 26(a)(2) (“Disclosure of Expert Testimony”) provides that “a party must disclose to the other parties the identity of any witness it may use at trial.” Fed.R.Civ.P. 26(a)(2)(A). This disclosure, unless otherwise stipulated or ordered by the court, “must be accompanied by a written report ... if the witness is one retained or specially employed to provide expert testimony in the case.” Fed.R.Civ.P. 26(a)(2) (B). The report must contain, in pertinent part, “a complete statement of all opinions the witness will express and the basis and reasons for them.” Fed.R.Civ.P. 26(a)(2)(B)®.

“The reason for requiring expert reports is ‘the elimination of unfair surprise to the opposing party and the conservation of resources.’ ” Reed v. Binder, 165 F.R.D. 424, 429 (D.N.J.1996) (internal quotation omitted). Nevertheless, the Third Circuit has made clear that it is unaware of any bright line rule requiring that every opinion by an expert be preliminarily stated in their expert report. See Hill v. Reederei F. Laeisz G.M.B.H., Rostock, 435 F.3d 404, 423 (3d Cir.2006) (allowing expert’s testimony, despite the fact that it exceeded the scope of his report, and noting that “the permissible scope of expert testimony is quite broad, and District Courts are vested with broad discretion in making admissibility determinations.”). With the framework in mind, the Court turns now to Defendants’ request.

DISCUSSION

Defendants request leave to file a reply expert report addressing the issue of secondary considerations which will presumably be raised by Plaintiff in its rebuttal expert report on the issue of invalidity. Defendants explain that, because Plaintiff bears the burden of coming forward with evidence of any secondary considerations of non-obviousness, they should be given *635 an opportunity to rebut Plaintiffs expert’s opinions on this subject. In the alternative, Defendants request that Plaintiff be required to address secondary considerations in its opening expert report, so as to provide Defendants with an opportunity to adequately respond to same. Defendants maintain that, under the current schedule, if Plaintiff chooses to present evidence of secondary considerations in its rebuttal expert report, Defendants’ experts will have no opportunity to respond. This result would be prejudicial in light of Federal Rule of Civil Procedure 26 because — according to Defendants — they would be forced to either disclose rebuttal opinions in their opening report without the benefit of knowing the opinions they are rebutting or run the risk of preclusion from testifying.

Plaintiff, on the other hand, argues that there is no reason to modify the Court’s current scheduling order. First, Plaintiff claims that it has already provided detailed secondary consideration contentions, and has supplemented those responses as discovery has progressed.

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598 F. Supp. 2d 632, 2009 U.S. Dist. LEXIS 13109, 2009 WL 427518, Counsel Stack Legal Research, https://law.counselstack.com/opinion/sanofi-aventis-v-barr-laboratories-inc-njd-2009.