Microbix Biosystems, Inc. v. BioWhittaker, Inc.

184 F. Supp. 2d 434, 2000 U.S. Dist. LEXIS 20928, 2000 WL 33678918
District Court, D. Maryland·Decided August 22, 2000·No. CIV.A.MJG-97-2525·Published·Cited by 8 cases

Opinion

MEMORANDUM AND ORDER

GARBIS, District Judge.

The Court has before it Plaintiffs Motion for Reconsideration of Summary Judgment and the materials submitted relating thereto. The Court finds a hearing unnecessary.

On December 21, 1999, Defendants Abbott Laboratories (“Abbott”), BioWhittaker, Inc. and BioWhittaker Holdings, Inc. (collectively “BioWhittaker”) moved for summary judgment on the antitrust claims brought by Plaintiff Mierobix Biosystems, Inc. (“Mierobix”). By Order dated March 28, 2000, this Court granted summary judgment on the antitrust claims, and further dismissed the substantively identical common law claim of tortious interference with economic relationships on the ground that the antitrust claims were not viable. Plaintiff now moves the Court to reconsider its March 28 Order. In addition, Plaintiff requests that certain changes be made to the separate March 28, 2000 Memorandum and Order Re Counterclaims in which the Court granted summary judgment to Mierobix on the theft of trade secrets claim.

I. MOTION FOR RECONSIDERATION

A. Legal Standard

A motion for reconsideration is granted only in limited circumstances. As stated by Judge Ramsey in Weyerhaeuser Corp. v. Koppers Co., Inc.:

A motion for reconsideration (or, to alter or amend judgment) made pursuant to Fed.R.Civ.P. 59(e) may be made for one of three reasons: (1) an intervening change in the controlling law has occurred, (2) evidence not previously available has become available, or (3) it is necessary to correct a clear error of law or prevent manifest injustice.

771 F.Supp. 1406, 1419 (D.Md.1991) (citation omitted). Such a motion “cannot be used to raise arguments which could, and should, have been made before [the determination to be reconsidered] issued.” Federal Deposit Ins. Corp. v. Meyer, 781 F.2d 1260, 1268 (7th Cir.1986) (citation omitted).

B. The Antitrust Claim

The Court previously granted Defendants summary judgment on the antitrust claims on the ground that Mierobix, as Plaintiff and the party opposing summary judgment, failed to present evidence suffi *437 cient to create a genuine dispute of material facts for trial. 1

In the Motion for Reconsideration, Plaintiff argues that there was evidence creating a genuine dispute of material facts for trial and that the Court imper-missibly preferred the Defendants’ version of the facts over that of Plaintiff. To support this argument, Plaintiff (1) merely reargues the facts and theories already ruled upon by the Court and (2) seeks to present new evidence 2 to generate a dispute of material fact for trial. Because the Motion for Reconsideration essentially reargues the issues already addressed sufficiently by the Court’s March 28 Order, the Court need not discuss these issues. Nevertheless, the Court shall clarify some of Plaintiffs apparent misunderstandings concerning the Court’s March 28 Order and the relevant legal standards, especially as they relate to the element of causation.

As a preliminary matter, the Court notes that in the antitrust context, Plaintiff must establish, inter alia, the fact of damages with a “fair degree of certainty.” See March 28 Order at 37. Moreover, Plaintiff has the burden of proving that the alleged illegal conduct was “a substantial or materially contributing factor” in its injury. Id. at 44. While the conduct that caused the Plaintiffs injury can be proven either by direct evidence or on the basis of circumstantial evidence and inference, evidence that is merely speculative 3 will not satisfy this burden. Id. at 44.

Viewing the “evidence” presented by Plaintiff in light of these relevant standards, the Court previously concluded:

Plaintiff has not presented evidence, other than conclusory allegations, that the lack of a long-term supply of HNK cells was a material cause of Gensia’s termination decision. At best, the evidence presented by Plaintiff shows that the exclusive agreement was one of the many factors—but not a substantial factor—contributing to Gensia’s. termination decision. Indeed, the evidence does not permit a finding that Gensia would have remained in the partnership even though confronted by (1) the FDA [Food and Drug Administration] ban, 4 *438 (2) Gensia’s unwillingness to make the financial commitments that Microbix requested, (3) the closure of the Cali, Colombia cell source, and (4) Microbix’s failure to enter into a partnership with a manufacturing facility.

March 29 Order at 39-40 (footnote in original). Plaintiff contends that this conclusion was factually unsupported because “Microbix produced ample evidence that Gensia terminated its partnership with Mi-crobix due to the exclusive supply agreement.” Pi’s Mot. for Recon. at 11-12. Specifically, Plaintiff argues that because Gensia did not have knowledge of the intervening events (e.g., the FDA ban), the events could not have caused Gensia to terminate the partnership. This argument is based upon an apparent misconception that Gensia’s knowledge of the independent intervening events was critical.

In the Court’s view, it is irrelevant what Gensia knew or did not know at the time it terminated the partnership with Microbix. Thus, the relevant inquiry before the Court was whether Gensia would have remained in the partnership with Microbix if Gensia eventually were confronted with the other intervening events that independently shut off the supply of HNK cells. Plaintiff, the party with the burden of proof, must introduce evidence that Gensia would have remained in the partnership in spite of the independent intervening causes. Because the evidence presented by Plaintiff concerning this issue was speculative at best, permitting the case to go to the jury would contravene Rule 56’s gate-keeping policy.

Similarly, Microbix apparently misinterprets the example provided by the Court to illustrate the speculative nature of Plaintiffs evidence in footnote 63 of the March 28 Order, which stated:

For example, it is undisputed that the FDA banned the import of HNK cells on September 18, 1998, and that Gensia terminated its partnership with Microbix after the ban, in November of 1998. In the absence of contrary evidence, a reasonable inference could be made that the FDA ban was a substantial factor contributing to the lack of long-term supply of HNK cells, which materially caused Gensia to end the partnership.

March 29, 2000 Order at 39-40 n. 63.

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Microbix Biosystems, Inc. v. BioWhittaker, Inc., 184 F. Supp. 2d 434, 2000 U.S. Dist. LEXIS 20928, 2000 WL 33678918 (D. Md. 2000).

184 F. Supp. 2d 434 (Microbix Biosystems, Inc. v. BioWhittaker, Inc.) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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