Mass Eye and Ear Inf v. QLT PhototherapeuticMass Eye and Ear Inf v. QLT Phototherapeutic
Donald R. Ware, with whom Barbara A. Fiacco, Jessica M. Silbey, Mark A. Reilly and Foley Hoag LLP, were on brief, for appellee/cross-appellant.
The entire range of claims articulated by plaintiff-appellant was dismissed by the district court on summary judgment. The bulk of the opinion that follows consists of our de novo review of these dismissals. We must also address defendant-appellee‘s cross-appeal of several discovery-related rulings. Following a review of the factual background, considered in the light most favorable to the appellant, we will begin our analysis.
I. Factual Background
A. Age-Related Macular Degeneration
Age-related macular degeneration (AMD) is an ocular disease that is the predominant cause of vision loss in people over age fifty. The illness takes two forms: “wet” and “dry.” The wet form, though only accounting for ten percent of the cases of age-related macular degeneration, leads to the debilitating condition known as choroidal neovascularization (“CNV” or “neovasculature“), responsible for ninety percent of cases of AMD vision loss. Neovasculature refers to conditions characterized by the proliferation of unwanted blood vessels.
The Massachusetts Eye and Ear Infirmary (“MEEI” or “the Infirmary“), a medical institution located next to, but distinct from, MGH, also sought out QLT‘s BPD for photodynamic therapy research. Dr. Joan Miller joined the Infirmary in the fall of 1991 and soon proposed conducting studies using BPD on monkeys. In March 1992, Miller applied to MEEI to investigate the use of BPD to treat neovasculature. Pursuant to Dr. Miller‘s application, MEEI and QLT signed a material transfer agreement (“MTA“) in which MEEI would receive BPD at no cost in exchange for providing QLT the results of Miller‘s pre-clinical studies for use in QLT‘s regulatory filings and patent disclosures.
In September 1992, following their successful monkey trials, which demonstrated the potential use of photodynamic therapy with BPD, Dr. Miller and her MEEI colleague, Dr. Gragoudas, presented their data confidentially to QLT representatives visiting
B. Confidential Disclosure Agreement
QLT had interest in commercial applications of the Infirmary‘s experimental monkey trials and, in May 1993, QLT and Dr. Miller entered into a Confidential Disclosure Agreement (“CDA“). As part of this agreement, QLT promised “not to use the Confidential Information for any purpose other than the evaluation of Products under the terms of this Agreement” and “to maintain Confidential Information in confidence.” The parties agreed that “misuse or improper disclosure of Confidential Information would irreparably harm the business of the disclosing party or that party‘s affiliates.” Pursuant to the CDA, Miller continued to provide MEEI‘s confidential research results to QLT, including results of MEEI research not funded by QLT.
In July 1993, at Dr. Miller‘s request, QLT agreed to fund further experiments by the Infirmary involving the treatment of neovasculature in monkeys with the derivatives. The results of these studies, as well as other studies not funded by QLT, were shared with QLT in November 1994, in a report entitled the Preclinical BPD-MA Pharmacology Study for Macular Degeneration (“Bolus Study“).
C. QLT Partnership with CIBA Vision
In late 1993, QLT contacted the company CIBA Vision1 to commercialize the use of photodynamic therapies with BPD to treat age-related macular degeneration. QLT provided CIBA Vision with MEEI‘s confidential research results without first informing MEEI. In February 1994, CIBA Vision sought full access to Dr. Miller‘s research results to pursue a “high potential opportunity.” QLT agreed to share with CIBA Vision the “plans and results of our ocular programme,” which included Dr. Miller‘s research.
Dr. Miller learned of QLT‘s negotiations with CIBA Vision in the Spring of 1994. In March, she expressed concern about the confidentiality of MEEI‘s research results to Julia Levy and Edwin Levy of QLT, who assured her that QLT had not disclosed and would not disclose in the future any of MEEI‘s trade secret information. Dr. Miller then flew to Switzerland “to get CIBA Vision excited in the technology,” but during that meeting, and subsequent meetings with CIBA Vision representatives in July and October of 1994 she presented only summaries of her research.
On May 31, 1994, CIBA Vision and QLT executed a Letter of Intent to enter into a strategic partnership for commercializing the use of photodynamic therapy to treat neovasculature arising from age-related macular degeneration. The Letter recognized that QLT had “significant non-clinical evidence” -- some of which came
Researchers at [MEEI] in Boston are participating in a joint worldwide project with [QLT] and CIBA . . . to develop photodynamic therapy, a potential treatment for certain eye diseases. Infirmary researchers, since 1992, have performed pre-clinical studies, in collaboration with Wellman Laboratories, using Benzoprophin derivative (BPD), a proprietary light-activated drug developed by [QLT].
Clinical trials testing the treatment on humans began in 1995, and the Infirmary was one of several sites performing the trials under a written agreement with QLT. MEEI was paid more than one million dollars for participation in the trials and for the resulting clinical data.
On February 6, 1995, QLT and CIBA Vision signed a definitive agreement to pursue worldwide joint development and commercialization of photo-dynamic therapy for the treatment of choroidal neovasculature. The partnership aimed to obtain FDA approval for its treatment, tradenamed Visudyne, in April 2000. Sales outside the United States began in 1999, and Visudyne received FDA approval in April 2000. As of February 2002, over two hundred twenty million dollars’ worth of Visudyne had been sold worldwide.
D. Patent Applications
Prior to QLT‘s partnering with CIBA Vision, in March 1994, Dr. Miller approached QLT about pursuing a patent application for the treatment. QLT agreed and suggested that Kate Murashige, its long-standing patent attorney, prepare the application. Relying on information provided by Miller, Murashige prepared a patent application with serial number 08/209,473 (“the ‘473 application“) and filed it on March 14, 1994. The claimed invention applied to methods for treating choroidal neovasculature with photodynamic therapy using BPD; the named inventors included only MEEI‘s Drs. Miller and Gragoudas and another MEEI employee, Lucy Young.
Even though it was not claiming co-inventorship of the ‘473 application, QLT confirmed that it would pay for the preparation of the application. Murashige told MEEI that “QLT does not see itself as a participant in the invention other than as a supplier of the material BPD,” and “the assignment would be entirely to MEEI.”
Within months of the ‘473 filing, however, QLT changed its approach to the patent strategy. On behalf of QLT, Murashige proposed to MEEI that the ‘473 application could be improved upon by modifying the scope of the patent claims. Murashige argued that it would strengthen the application to include methods of treating CNV with photo-dynamic therapy using liposomal formulations of BPD.
at the time the invention was made, there was no contractual agreement in place whereby QLT would be entitled to ownership of the invention. Therefore QLT claims ownership only through Dr. Julia Levy . . . . If Dr. Levy were not an inventor, QLT would have no rights to the patent.
Thus, Murashige convened the three institutions -- QLT, MEEI, and MGH -- and requested that MEEI and MGH retain their own patent counsel.
Implementing the proposal entailed a “continuation-in-part application,” with serial number 08/390,591 (the ‘591 application). At the same time, Murashige removed from the ‘473 applications those claims directed to methods of treating unwanted choroidal neovasculature with photodynamic therapy using the benzoporhin derivatives. Those claims were joined to the ‘591 application.
After receiving assurances that MEEI would receive fair compensation for its contributions, the MEEI inventors consented to the changes, and Murashige filed the ‘591 application on February 17, 1995. MEEI‘s Miller and Gragoudas executed a
On August 25, 1998, the ‘591 application issued as U.S. Patent 5,798,349 (the ‘349 patent). Drs. Miller and Gragoudas assigned their rights as inventors to the Infirmary, and Drs. Hasan and Schmidt-Erfurth assigned their rights to MGH. Dr. Levy assigned her rights to QLT. Among the assignees of the inventorship of the ‘349 patent, QLT is distinguished by its ownership of the patents on the benzoporphin derivatives integral to the invented treatment. This ownership means that QLT alone can independently exploit the rights of the ‘349 patent.
E. Licensing Negotiations
In December 1995, QLT had signed a letter of intent to negotiate exclusive licenses of MEEI‘s and MGH‘s co-ownership rights in any patent that issued from the pending ‘591 application. Such a license would prevent MGH or MEEI from licensing their
MEEI responded in February 1996 that the Letter of Intent “is insufficient in that it does not address the issue of how the Infirmary will participate in the licensing or transferring of MEEI technology by QLT to third parties.” MEEI also accused QLT of entering into an agreement with CIBA Vision “using, in part, technology that was developed . . . at the Infirmary.” MEEI concluded, “If that is untrue, please advise us. If that is true, our position is that the Infirmary should be a party to that agreement as well as any future agreements relative to that technology.” QLT did not respond to this letter.
II. QLT‘s Cross-Appeal
The above narrative anticipates the disposition of the cross-appeal, as the picture we have painted includes information
QLT contends that the district court erroneously ordered the production of certain attorney-client communications with Murashige and other attorneys of her firm. The district court found that QLT met its burden of establishing the prima facie applicability of the attorney-client privilege to the communications in question. See Mass. Eye & Ear Infirmary v. QLT Phototherapeutics, Inc., 167 F. Supp. 2d 108, 115 (D. Mass. 2001) (accepting report and recommendation of discovery master). Such communications are privileged unless an exception -- here, the common-interest exception -- applies. The party challenging the privilege carries the burden of establishing that any communications are discoverable. FDIC v. Ogden Corp., 202 F.3d 454, 460 (1st Cir. 2000). The common-interest exception permits a party access to his joint-client‘s communications with the shared counsel. The district court held that the common-interest exception applied, within a specified time frame and as to certain
We disturb a district court‘s discovery management “only upon a clear showing of manifest injustice, that is, where the lower court‘s discovery order was plainly wrong and resulted in substantial prejudice to the aggrieved party.” Mack v. Great Atl. & Pac. Tea Co., 871 F.2d 179, 186 (1st Cir. 1989). QLT invites us to conduct a plenary review of the relevant orders, arguing that whether an exception to the attorney-client privilege applies is a question of law that deserves de novo review, citing Cavallaro v. United States, 284 F.3d 236, 245 (1st Cir. 2002). The authority QLT cites, however, specifies only that the “formulation of . . . the . . . common-interest doctrine” should be reviewed de novo. Id. (emphasis added). The application of properly formulated doctrine to the facts remains a matter of discretion for the district court. Id.
The discovery master spelled out MEEI‘s burden as follows:
MEEI must first establish that MEEI shared an attorney-client relationship with Morrison & Foerster [Murashige‘s law firm] on the following matters: (1) the preparation and prosecution of the ‘473 application (which issued as the ‘986 patent); (2) the preparation and prosecution of the ‘591 application (which issued as the ‘349 patent); (3) the licensing of the ‘986 patent; and (4) the licensing of the ‘349 patent.
It is peculiar to address this question first as it inevitably requires reaching into the merits we have yet to discuss. But the district court had to do so, as must we. The irony that the ensuing discovery shows just how polarized the two parties’ interests may already have been is not material to the inquiry. “A joint attorney-client relationship remains intact until it is expressly terminated or until circumstances arise that readily imply to all the joint clients that the relationship is over.” Ogden, 202 F.3d at 463. The rules of discovery therefore do not insulate from discovery the communications of a duplicitous party who feigns common interest while scheming otherwise with a shared, trusted advisor.
We agree, for the reasons elaborated in the master‘s recommendation, 167 F. Supp. 2d at 118-23, that QLT and MEEI were
The district court found an endpoint to joint-client status as of October 1, 1998:
There is no evidence in the record that MEEI‘s and QLT‘s joint attorney-client relationship with Morrison & Foerster for the preparation and prosecution of the ‘473 application, or for the preparation and prosecution of the ‘591 application, was expressly terminated.
However, in a letter dated October 1, 1998, MEEI informed QLT that MEEI had filed in the PTO a continuation patent application of the ‘591 application. From the record, it is clear that neither QLT nor Morrison & Foerster was involved in the preparation or prosecution of the continuation patent application. Thus, . . . at least as of October 1, 1998, both MEEI and QLT understood that their respective legal interests in the ‘349 patent were no longer the same, or nearly the same, legal interest.
. . .
It is less clear when MEEI‘s and QLT‘s respective legal interests in the ‘986 patent
were no longer the same, or nearly the same, legal interest . . . . [However], at least as of October 1, 1998, both MEEI and QLT understood that their respective legal interests in the ‘986 patent were no longer the same, or nearly the same, legal interest.
Mass. Eye & Ear Infirmary, 167 F. Supp. 2d at 126.
QLT does not disagree, but instead raises as an alternative argument in its appeal that, if it shared a common interest with MEEI, the common interest would have terminated more than a year earlier, at the latest on July 31, 1997. On that date, MEEI contested, by letter, QLT and MGH‘s role in the ‘591 invention. The letter from MEEI‘s patent attorney, Edmund Pitcher, to Murashige, expressed MEEI‘s view that “the entirety of the subject matter of the allowed claims is the invention of MEEI personnel only, and that neither Dr. Levy [of QLT], nor Drs. Hasan or Schmidt [of MGH] made any inventive contribution.” Pitcher noted that “Dr. Levy‘s presence on the application places MEEI in the uncomfortable position of being dependent on the fairness of QLT, despite its directly adverse economic interest, in the negotiation of a license agreement.” The letter included the demand that QLT:
make a concrete license proposal immediately and/or file a continuation application to permit correction of the named inventors. If the Infirmary and QLT cannot come to an agreement on a reasonable royalty rate and other financial terms, we are instructed to assume responsibility for prosecution of patent applications covering subject matter
invented without the involvement of Dr. Levy so as to try to preserve MEEI‘s rights.
QLT responded to the district court‘s order with a “Motion to Amend Order as to Date of Termination of ‘Common Interest,‘” in which QLT, for further support, drew on letters and memoranda written by Murashige and employees from QLT and CIBA Vision subsequent to MEEI‘s July 31 letter. In QLT‘s motion, QLT argued that MEEI‘s letter implied to QLT that it no longer shared the same interest in the successful prosecution of the ‘591 application, as MEEI was threatening to pursue an alternative and conflicting avenue for realizing federal protection for its invention. Thus, QLT contended that “as a matter of fact, as a result of MEEI‘s July 31, 1997 letter, QLT appreciated that QLT and MEEI no longer shared a common interest in successfully prosecuting the claimed inventions in” the ‘591 application.
The discovery master denied the motion to move the date of termination of interest forward, finding, in essence, that MEEI‘s conflicting interest was only conditional. That is to say, MEEI shared QLT‘s interest in the successful prosecution of the ‘591 application so long as a reasonable royalty rate was in the cards. MEEI argues that it “was merely exploring other possibilities of protecting its rights in the event that QLT did not live up to its promises once the ‘349 patent issued,” when it filed the 1997 application. The discovery master discussed how the letters and memoranda QLT offered supported this interpretation.
the memorandum [to] show[] that QLT understood that MEEI remained interested in the successful prosecution of the ‘591 application. Thus, contrary to QLT‘s assertions, the Kaufmann-Shaw Memorandum does not show that QLT implied, from the Pitcher Letter and the Finn Letter, that MEEI was no longer interested in the successful prosecution of the ‘591 application.
May 29, 2002, slip op. at 3.3
We believe that whether the common-interest exception expires upon the implication that a party has a conditionally adverse interest of the sort at issue here is a question of law over which we should exercise de novo review. The question is
III. MEEI‘s Appeal
The pivotal moment that shapes nearly all of MEEI‘s claims involves the filing of the continuation-in-part ‘591 application, which added Dr. Julia Levy of QLT and Drs. Schmidt-Erforth and Hasan of MGH as inventors on the patent. In the course of that switch in patent strategy, QLT made numerous assurances to MEEI that it would license MEEI‘s patent rights on reasonable terms. This case is before us because no licensing agreement was ever reached. MEEI claims that it was injured by this failure, and further harmed by QLT‘s unlawful disclosure of MEEI‘s trade secrets.
A. Contract Claims
1. Breach of Contract
The parties’ disagreement regarding the existence of an enforceable contract is a legal one, and so this court reviews the question of contract formation de novo. Coady v. Ashcroft & Gerel, 223 F.3d 1, 10 (1st Cir. 2000). The district court determined that the parties failed to reach an agreement whose terms were sufficiently determinate to constitute a binding contract. MEEI counters that the district court erred in failing to recognize that a valid contract could include terms defined by industry standards. While there are surely some contracts in which a crucial term could be sufficiently defined by pegging it to industry standards, we agree with the district court‘s conclusion that there is insufficient evidence in the record to find that the parties had reached a meeting of the minds. See, e.g., Lucey v. Hero Intern. Corp., 281 N.E.2d 266, 269 (Mass. 1972) (finding that “‘[a]n agreement to enter into a contract which leaves the terms of that contract for future negotiation is too indefinite to be enforced‘“) (quoting Cygan v. Megathlin, 96 N.E.2d 702, 703 (Mass. 1951)).
MEEI has also claimed breach of contract with regard to the May 1993 Confidential Disclosure Agreement signed by QLT and Dr. Miller. We agree with the district court that MEEI was not a party to this agreement and that there is no evidence that Miller was acting as an agent of MEEI. Furthermore, MEEI does not fall
2. Breach of Implied Contract
We construe MEEI‘s breach of implied contract claim to be a claim of contract implied-in-fact rather than contract implied-in-law. Although both causes of action exist in Massachusetts,
“A contract implied in fact requires the same elements as an express contract and differs only in the method of expressing mutual assent.” 6 William Meade Fletcher et al., Fletcher Cyclopedia of the Law of Private Corporations § 2580 (perm. ed. rev. vol. 2004). Thus, MEEI‘s implied contract claim fails for the same reason we have rejected its express contract claim -- failure to reach agreement on the basic terms of the contract. In the prototypical implied contract case, the terms are already sufficiently clear, and the court looks to the actions of the parties only to determine whether their actions indicate that they, in fact, agreed on those terms. However, in this case, where the terms proposed by each side remain at odds, searching the actions of the parties for indicia of consent becomes a fruitless exercise. Without agreement on the essential terms of the agreement, MEEI‘s implied contract claim gets no further than does its express contract claim.
3. Breach of Covenant of Good Faith and Fair Dealing
Having concluded that no contract exists, there can be no derivative implied covenant of good faith and fair dealing
B. Conversion and Misrepresentation Claims
1. Conversion
MEEI claims that QLT converted MEEI‘s intellectual property rights in the invention of the photodynamic therapy “by causing MEEI to file a joint patent application with MGH and QLT so that a patent issued would name employees of all these institutions as inventors.” “Conversion requires the exercise of dominion or
2. Misrepresentation
MEEI claims that QLT falsely represented to MEEI that MEEI would be adequately compensated for its role in the inventions included in the ‘349 patent. In order to succeed on its misrepresentation claims, MEEI must show that QLT did not intend to comply with these representations at the time they were made. See Doyle & H.P. Leasing, Inc. v. Hasbro, Inc., 103 F.3d 186, 194 (1st Cir. 1996) (“plaintiffs must allege (1) that the statement was
C. MEEI‘s Motion to Amend
“We review the denial of a motion to amend under
MEEI made its motion to amend more than two years after filing the complaint, after the court had entered summary judgment for QLT on Counts I-IV of MEEI‘s complaint and the parties had fully briefed summary judgment arguments on the remaining four counts. “Where the motion to amend is filed after the opposing party has timely moved for summary judgment, a plaintiff is required to show ‘substantial and convincing evidence’ to justify
D. Unjust Enrichment
The district court believed that MEEI‘s unjust enrichment claim “distill[ed] into a disagreement over the inventorship in the ‘349 patent.” Based on that premise, the district court reasoned that MEEI could not use a Massachusetts unjust enrichment claim to circumvent federal patent law, and accordingly, granted summary judgment to QLT. We find, however, that the district court
While the proper inventorship of either the ‘473 application or the ‘591 application is indeed a non-negotiable question of federal law, the question of which application to prosecute was a choice available to the parties. Under the U.S. patent scheme, inventors have discretion to articulate the scope of their patent claims. Donald S. Chisum, 3-8 Chisum on Patents, § 8.06[4], at 8-247 (2003) (“An applicant may present more than one claim and is afforded reasonable latitude in varying the scope and terminology with which he defines his invention.“). MEEI‘s original ‘473 application‘s primary claim involved three main green porphyrin-based methods: a “method to treat conditions of the eye characterized by unwanted neovasculature” (claim 1); a “method to treat pigmented tumors in the eye” (claim 10); and a “method to observe the condition of blood vessels in the eye” (claim 19). The three methods had much in common: each claim involved administering green porphyrin, which would then localize in the blood vessels in the eye; the diagnostic method simply involved observing the vessels, and the two treatment methods involved irradiating the neovasculature or tumor with light. Furthermore, each method had an associated but separate claim that specified that “said green porphyrin is contained in a liposomal preparation” (claims 7, 16,
In December 1994, Murashige suggested substantially changing the scope and inventorship of the ‘473 application. First, she recommended spinning off the diagnostic method as a separate patent which would be “properly assignable solely to MEEI.” Second, she recommended combining the separately stated methods for treatment of neovasculature (claim 1) and treatment of pigmented tumors (claim 10) into a single method. The goal was to “be able to claim treating conditions of the eye more broadly,” i.e., expand the scope of the patent. In order to do this, however, it was necessary to “introduce the limitation of using the green porphyrin in a liposomal composition.” To this end, Murashige proposed a modified claim 1 that claimed “administering . . . green porphyrin in a liposomal composition.” As Murashige acknowledged, that “is substantially the same as claim 1 in the original case except that the limitation of using a liposomal composition has been included.”
Murashige explained the significance of this proposal. On the one hand, by broadening claim 1 “to claim treating conditions of the eye more broadly,” the patent, if granted, would have “potentially broader coverage than contemplated [earlier].” But the only way to justify these broad claims was to “introduce
However, this change to claim 1 broadened not just coverage of potential eye treatments, but also the list of inventors. Murashige explained that “if we include conditions of the eye generally using liposomal compositions, . . . a larger circle of inventors would be included both because of this greater breadth and by virtue of the necessity to supply the green porphyrin in liposomes. It then appears that the inventorship would properly include . . . Julia Levy . . . .” In other words, the very aspect of the application that was “a liberating device, allowing [the inventors] to claim more broadly” also happened to be the aspect of the revised application that would require adding Dr. Levy as an inventor. (Conversely, had liposomal preparations not been claimed at all, arguably the patent would be less valuable, but Dr. Levy might not be an inventor.) Adding Dr. Levy, of course, would give QLT full co-ownership rights to exploit the patent. Thus, QLT presented MEEI with a second viable formulation of its patent application: it asked MEEI to change the scope of its patent application to QLT‘s benefit in exchange for fair compensation.5
MEEI already possessed a valid, and seemingly defensible, patent application, when QLT sought MEEI‘s assent to replace the ‘473 application with the ‘591 application.6 QLT acknowledged that the patent as MEEI envisioned it (without Levy and her claims) would be difficult to challenge on grounds of either obviousness or noninventorship. Nevertheless, QLT argued that the patent could be made stronger -- in some ways both broader and more defensible -- by changing the scope of the patent and adding the additional inventors who participated in the new claims. The addition of QLT inventor Dr. Levy, however, would drastically reduce MEEI‘s potential profits from the patent. If MEEI agreed to the ‘591 application with the additional inventors, QLT would no longer need a license in order to commercialize the photo-dynamic therapy that became known as Visudyne. Since QLT already owned the other
Not surprisingly, MEEI did not initially agree with this new approach proposed by QLT. Attorney Murashige nevertheless prepared the ‘591 continuation-in-part application, and MEEI eventually assented after being promised fair compensation for its contribution. Of course, MEEI and QLT never came to an agreement on the critical compensation figures, and it is for that reason that we have affirmed summary judgment for QLT on MEEI‘s contract claims. This inadequate meeting of the minds does not, however, call for summary judgment in the context of unjust enrichment. A claim of unjust enrichment is appropriate “where an agreement is too indefinite to be enforced . . . [or] where no contract is made because each of the parties had a materially different understanding of the terms.” 1-1 Corbin on Contracts, § 1.20(b) (2004). Unjust enrichment provides an equitable stopgap for occasional inadequacies in contractual remedies at law by mandating that “[a] person who has been unjustly enriched at the expense of another is required to make restitution to the other.” Fox v. F & J Gattozzi Corp., 672 N.E.2d 547, 552 (Mass. App. Ct. 1996)
Furthermore, this analysis of MEEI‘s unjust enrichment claim illustrates why it was not preempted by federal patent law. MEEI‘s claim is not that Dr. Levy was not a proper inventor of the ‘349 patent, but rather that QLT induced MEEI to agree to the change in scope of the claims, and then unjustly profited from that change by denying fair compensation. In these circumstances, conflict preemption, not the broader field preemption, is appropriate. See Hunter Douglas, Inc. v. Harmonic Design, 153 F.3d 1318, 1334-35 (Fed. Cir. 1998). Under the conflict preemption standard, if the tort action is based on conduct that is not “protected or governed by federal patent law,” then “the remedy is not preempted.” Id. at 1335; compare Univ. of Colo. Found., Inc. v. Am. Cyanamid Co., 196 F.3d 1366, 1372 (Fed. Cir. 1999) (independent state law inventorship standards frustrate basic objectives of patent law and thus entire field of inventorship is preempted) with id. at 1373-74 (unjust enrichment claim preempted only because it “hinge[d]” on a determination of inventorship).
QLT argues that MEEI‘s claims are preempted by
We recognize that the preemption issue here is close. It is true that allowing MEEI‘s claim to proceed would, to some
We also note that, while there is no direct precedent concerning preemption under
Here, the allegation is that the defendant manipulated the plaintiff into agreeing to change the scope of the patent so as to include contributions made by the defendant. MEEI has not provided evidence that QLT‘s alleged conduct was actually fraudulent. However, arguably, the case for preemption here is weaker than in the cited cases. In the cited cases, the plaintiff struck at the heart of inventorship by arguing (essentially) that the patent was applied for fraudulently and never should have issued. Here, the plaintiff argues that the defendant induced plaintiff to agree to a certain scope of invention in exchange for compensation, and then provided none.
We also draw an analogy from the doctrine of inequitable conduct before the Patent and Trademarks Office (PTO).12 Courts have distinguished state claims alleging bad faith misconduct by the applicant against the PTO -- which are preempted -- from state claims alleging bad faith misconduct occurring subsequently in the marketplace -- which are not. See, e.g., Methode Elecs. Inc. v. Hewlett-Packard Co., 55 U.S.P.Q.2d 1602, 1604-05 (N.D. Cal. 2000)
In other words, state claims alleging misconduct before the PTO are preempted because federal law contains a specific remedy for just such misconduct. Even then, not all state claims that implicate the issue of inequitable conduct before the PTO are preempted. See Dow Chem. Co. v. Exxon Corp., 139 F.3d 1470, 1471 (Fed. Cir. 1998)
Again, this precedent is not directly on point. The distinction cited above is between state claims alleging misconduct by an applicant against the PTO (which are usually, if not always, preempted), and claims alleging misconduct between parties after the patent has issued. Here, the claim is misconduct by an applicant against a co-applicant before the application is completed. But misconduct between parties before the patent issues is more analogous to misconduct between parties after the patent issues than it is to misconduct by a party against the PTO.
For all these reasons, MEEI‘s unjust enrichment claim is not preempted.
We also find that MEEI‘s unjust enrichment claim should survive summary judgment based on the allegations of QLT‘s misuse of confidential information. Under Massachusetts law, “[a] constructive trust is . . . imposed to avoid the unjust enrichment of one party at the expense of the other where ‘information confidentially given or acquired was used to the advantage of the recipient at the expense of the one who disclosed the information.‘” Mass Cash Register, Inc. v. Comtrex Sys. Corp., 901 F. Supp. 404, 423 (D. Mass. 1995) (quoting John Alden Transp. Co. v. Arnold Bloom, 415 N.E.2d 250, 250 (Mass. App. Ct. 1981)). The facts underlying this theory will be laid out in the course of our subsequent trade secret claim analysis.13
E. Trade Secret and Unfair Trade Practices Claims
The right to control how research is used and who is privy to trade secrets is crucial to protecting the economic interests of non-profit research institutions like MEEI, just as it is essential to for-profit businesses. Without the ability to guard their own data, there would be fewer incentives for
1. Misappropriation of Trade Secrets
MEEI claims that QLT misappropriated its trade secrets without MEEI‘s knowledge, in particular, by disclosing certain research results to QLT‘s eventual partner, CIBA Vision. MEEI argues that the district court erred in concluding that MEEI‘s trade secret claim was time barred by the three-year statute of limitations for tort actions because, under Massachusetts law, the statute should have been tolled.
Massachusetts law establishes two avenues by which the three-year statute of limitations that would ordinarily apply to MEEI‘s trade secret claims can be tolled. The Massachusetts common law “discovery rule” provides that the statute of limitations is tolled “until a plaintiff knows, or reasonably should have known, that it has been harmed or may have been harmed by the defendant‘s conduct.” Taygeta Corp. v. Varian Assocs., Inc., 763 N.E.2d 1053, 1063 (Mass. 2002). “The appropriate standard to be applied when assessing knowledge or notice is that of a ‘reasonable person in
Massachusetts statutory law also grants a reprieve from the statute of limitations when a potential defendant fraudulently conceals the basis for a cause of action:
If a person liable to a personal action fraudulently conceals the cause of such action from the knowledge of the person entitled to bring it, the period prior to the discovery of his cause of action by the person so entitled shall be excluded in determining the time limited for the commencement of the action.
The district court made short work of MEEI‘s trade secrets claims by finding that MEEI had actual knowledge of its claims more than three years before bringing this suit on April 24,
a. Review of District Court Summary Judgment Decision
Summary judgment is appropriate when “the pleadings, depositions, answers to interrogatories, and admissions on file, together with the affidavits, if any, show that there is no genuine issue as to any material fact and that the moving party is entitled to judgment as a matter of law.”
“Our review of the district court‘s grant of summary judgment is plenary, and we read the record in the light most amicable to the party contesting summary judgment.” Cambridge Plating Co. v. Napco, Inc., 991 F.2d 21, 24 (1st Cir. 1993) (reversing the district court grant of summary judgment because material facts remained at issue where plaintiff knew it had been
The district court seems to have given little weight to MEEI‘s claims that QLT repeatedly reassured Miller that it was not disclosing any confidential information. Rather, the district court found that in a 1996 letter to QLT, MEEI indicated that it
b. Applying Massachusetts Tolling Law
We have held that “the Massachusetts court does not equate suspicion with knowledge, but is explicit in requiring actual knowledge, or, as an equivalent, full means of detecting the fraud.” Id. (internal quotation omitted). The district court rejected MEEI‘s reliance on Tracerlab, because it found that the 1992 letter, among other evidence, showed that MEEI actually believed it had a cause of action for trade secret misappropriation. The district court believed that plaintiffs
However, we find Tracerlab instructive. As in this case, the plaintiffs in Tracerlab knew that the defendants possessed the trade secrets in question. Id. at 99 (“There is no question but that [the plaintiff] was aware from the beginning that [the defendants] knew plaintiff‘s trade secrets” because they were former employees of the plaintiff.) Furthermore, in Tracerlab, the court found that the plaintiff was “well aware from the very outset that [the defendants] had gone into the [same] field and were producing a competitive product.” Id. at 100. Still, in that case, we found that “all of this is a far different thing from having knowledge that the defendant had misappropriated and was using the self-same . . . trade secrets . . . underl[ying] the present cause of action.” Id. Moreover, unlike most trade secret cases, during much of the time in question in this case, use of MEEI‘s trade secrets by data recipients like CIBA Vision would still have remained behind closed doors, as product development was not yet complete. Therefore, MEEI was even less likely to become aware of any unauthorized disclosures.
“Although the Massachusetts legislature has set statutory limitations periods for various causes of action[,] . . .
Although it is true that “[t]he plaintiff need not know the full extent of the injury before the statute starts to run,” Bowen, 557 N.E.2d at 741 (emphasis added), the district court incorrectly expanded this principle to find that MEEI need not know “the full extent of its claim.” Mass. Eye & Ear Infirmary v. QLT Phototherapeutics, Inc., No. 00-10783, at 12 (D. Mass. Apr. 23, 2002) (sealed memorandum in support of summary judgment). This is not a case in which MEEI claims only that it did not know how much it had been harmed; rather, MEEI claims that it did not know that it had been harmed at all.
c. MEEI‘s Awareness of Some of QLT‘s Misappropriations
In order for the statute of limitations to start to run, “an event or events [must] have occurred that are reasonably likely to have put the plaintiff on notice that he has been harmed.” Stark, 736 N.E.2d at 442 (citing Bowen, 557 N.E.2d at 741). We do not believe that in a complex case of this nature -- where trade secrets of varying importance are alleged to have been divulged
MEEI has not denied knowledge of some of QLT‘s alleged trade secrets misappropriations. The record does not, however, indicate that MEEI knew of all, or substantially all, such misappropriations. Furthermore, MEEI‘s claims are strengthened by the existence of the Confidentiality Agreement and QLT‘s repeated assurances that its trade secrets were not being disclosed. To assume that MEEI knew the full extent of disclosure to CIBA Vision would be to assume that MEEI was already aware that it was on the verge of being cut out of any future profits from the newly developed photodynamic therapy. Though this may be the case, we do
QLT points out that MEEI does not claim that it gained any additional knowledge in the years prior to filing suit in 2000, and thus MEEI could just as easily have filed suit more than three years prior. However, this fact alone is not sufficient to show that MEEI should have filed suit earlier. Because of the nature of the claim, it is possible that some of MEEI‘s trade secret claims were only shots in the dark at the time MEEI filed its complaint, and that MEEI only learned of the facts substantiating some of its claim after receiving discovery. Although the fact that a plaintiff files suit is usually strong evidence that he knows the facts underlying each of his own claims, filing suit does not prove, in itself, that he has sufficient knowledge to prevent tolling of the statute of limitations.
d. Fraudulent Concealment or Breach of Fiduciary Duty
Since the district court found that MEEI had actual knowledge of QLT‘s alleged misappropriations, it did not need to reach the question of whether QLT actively concealed its disclosures of MEEI‘s trade secrets. Having found that the issue of MEEI‘s knowledge of its trade secret claims was not properly decided on summary judgment, we believe that MEEI‘s claims based on fraudulent concealment should also survive summary judgment.
In addition, MEEI‘s claim that QLT owed fiduciary duties to MEEI has some persuasive force. Fiduciary duties exist “when a party to a contract expressly repose[s] a trust or confidence in the other party” or “where the contract or transaction was intrinsically fiduciary and, therefore, required perfect good faith.” 26 Richard A. Lord, Williston on Contracts, § 69:23 (4th ed. 2004). By entering into their joint research relationship, MEEI and QLT each put their valuable trade secrets in the others’ hands, arguably requiring full disclosure of any misappropriation of those secrets. Furthermore, in Massachusetts, if a defendant fails to learn of a trade secret violation due to a fiduciary‘s
e. MEEI‘s Late Addition of Trade Secret Claims
MEEI provided no credible explanation for its delayed attempt to amend its complaint, and thus, we cannot say that the district court abused its discretion in refusing to allow MEEI to assert additional claims based on QLT‘s alleged disclosure of the results of the Preclinical Bolus Study and its visual acuity data. See, Torres-Ríos v. LPS Labs., Inc., 152 F.3d 11, 16 (1st Cir. 1998); Hayes v. New Eng. Millwork Distribs., 602 F.2d 15, 19 (1st Cir. 1979).
2. Unfair Trade Practices
The district court held that its “previous rulings on Contract and Trade Secret Claims,” as well as MEEI‘s other claims, “indicate there is no basis, on these facts, for a 93A claim.”
Massachusetts General Law ch. 93A, § 2 provides that “[u]nfair methods of competition and unfair or deceptive acts or practices in the conduct of any trade or commerce” are unlawful.
IV. Conclusion
For the foregoing reasons, the judgment of the district court is affirmed in part and reversed and remanded in part.
Affirmed in part and reversed and remanded in part. No costs.
Notes
279 U.S. at 391.[The inventor]‘s right was independent of and prior to any arising out of the patent law, and it seems a strange suggestion that the assertion of that right can be removed from the cognizance of the tribunals established to protect it by its opponent going into the patent office for a later title. It is said that to establish [the inventor]‘s claim is to invalidate Becher‘s patent. But, even if mistakenly, the attempt was not to invalidate that patent but to get an assignment of it, and an assignment was decreed. Suits against one who has received a patent of land to make him a trustee for the plaintiff on the ground of some paramount equity are well known.
210 A.2d at 98 (internal citations omitted).[The complaint] depends on principles of common law and equity governing fraud and disparagement, and plaintiff‘s rights are dependent upon such principles. Plaintiff has not sought a declaratory judgment to void the patent on the federal grounds of non-invention. Nor has he based
his claim for disparagement on the invalidity of the patent. Instead, plaintiff claims ownership of an interest in the patent, and demands an assignment of that interest and damages resulting from slander of his ownership.