Alzheimer's Institute of America, Inc. v. Avid Radiopharmaceuticals

952 F. Supp. 2d 740, 85 Fed. R. Serv. 3d 1299, 2013 WL 3305743, 2013 U.S. Dist. LEXIS 91795
CourtDistrict Court, E.D. Pennsylvania
DecidedJuly 1, 2013
DocketCivil Action No. 10-6908
StatusPublished
Cited by1 cases

This text of 952 F. Supp. 2d 740 (Alzheimer's Institute of America, Inc. v. Avid Radiopharmaceuticals) is published on Counsel Stack Legal Research, covering District Court, E.D. Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Alzheimer's Institute of America, Inc. v. Avid Radiopharmaceuticals, 952 F. Supp. 2d 740, 85 Fed. R. Serv. 3d 1299, 2013 WL 3305743, 2013 U.S. Dist. LEXIS 91795 (E.D. Pa. 2013).

Opinion

MEMORANDUM OPINION

SAVAGE, District Judge.

In its posLtrial motion seeking judgment as a matter of law or a new trial, plaintiff Alzheimer’s Institute of America (“AIA”) challenges the jury verdict finding that Michael Mullan was not the sole inventor and that John Hardy, at least, was a co-inventor of the Swedish mutation inventions that are the patents-in-suit, and that the University of South Florida (“USF”) did not waive its rights to the inventions.1 With the exception of its sufficiency of the evidence argument, AIA’s grounds for judgment as a matter of law are the sáme as those it made at the [744]*744summary judgment stage.2 Nothing occurred at trial or since our ruling on the summary judgment motions that has any effect on our interpretation of the law and its application to this case. For the same reasons given in our summary judgment opinion,3 we reject AIA’s renewed arguments that the Florida regulation4 is preempted by federal law, USF’s failure to comply with certain of the regulation’s requirements voided any ownership rights it may have had in the Swedish mutation invention, and the only manner in which USF could obtain legal title to the patents is via a written assignment pursuant to 35 U.S.C. § 261.

As to the sufficiency of the evidence, any reasonable jury could have concluded from the evidence that Hardy was a co-inventor of the patented invention. Likewise, there is ample evidence to support the jury’s finding that USF had not waived its ownership rights in the inventions. Therefore, we shall deny AIA’s motion for judgment as a matter of law.

The motion for new trial attacks jury instructions on inventorship and waiver, and evidentiary rulings excluding certain documents. The complaints about the jury instructions are derivative of those made in the motion for judgment as a matter of law, that is, AIA complains that the instructions were consistent with our rulings which AIA contend were legally incorrect. Because the jury instructions correctly stated the law and the precluded evidence was properly excluded, the motion for new trial will also be denied.

Co-Inventorship

AIA contends that there was a lack of “substantial evidence” upon which the jury could find that Hardy had made a “significant contribution to the conception” of the invention, qualifying him as a co-inventor.5 Relying on Amgen, Inc. v. Chugai Pharmaceutical Co., 927 F.2d 1200 (Fed.Cir. 1991), AIA argues that there was no evidence that Hardy contributed to the “discovery of the location, structure, or physical properties of the Swedish mutation, as required for conception of a DNA invention under Amgen.”6 As a corollary argument, AIA challenges the jury instruction on conception, claiming it failed to inform the jury that Hardy could only have been a co-inventor “if he contributed significantly to identification of the location and structure of the mutation.”7 (emphasis in original).

We start with the analysis of what constitutes a significant contribution to the conception of the Swedish mutation. Must it be as specific as AIA contends? Stated differently, to qualify as an inventor, did Hardy have to discover the precise “location, structure, or physical properties” of the Swedish mutation?8

AIA confuses contribution and conception. Its argument overlooks the fundamental difference between the two concepts. Two or more persons may work [745]*745together, not necessarily in time and place, to reach the point of conception, but not all may be actively involved at the precise moment of conception. Each one of them is an inventor so long as he or she made a significant contribution to the conception. Hence, a qualifying significant contribution may precede conception.

AIA’s reading and interpretation of Amgen ignores the warning in Fina Oil and Chemical Co. v. Ewen, 123 F.3d 1466, 1474 (Fed.Cir.1997), that the doctrine of simultaneous conception and reduction to practice “cannot be used .... to show that because the first person did not conceive or reduce to practice the entire claim of the invention, he or she did not at least contribute in some significant way to the ultimate conception.” Instead, AIA seeks to impose a stricter standard for joint inventorship than the law requires. Applying AIA’s proffered standard would eliminate joint inventors and denigrate their significant contributions to an invention.

Joint inventorship is governed by the patent statute itself. 35 U.S.C. § 116. Two or more persons may be deemed joint inventors even though they did not physically work together on the invention or at the same time or make the same type or amount of contribution to every claim of the patent. Id. “This provision sets no explicit lower limit on the quantum or quality of inventive contribution required for a person to qualify as a joint inventor. Rather, a joint invention is simply the product of a collaboration between two or more persons working together to solve the problem addressed.” Fina Oil, 123 F.3d at 1473 (citing Burroughs Wellcome Co. v. Barr Labs., Inc., 40 F.3d 1223, 1227 (Fed.Cir.1994)). Nevertheless, not all participation in the developmental or experimental process constitutes contributionship for purposes of joint inventorship status. To qualify as a joint inventor, one must make a significant contribution to the conception of the invention. See Fina Oil, 123 F.3d at 1473. In other words, a joint inventor must make a significant contribution on the road to and not necessarily at reaching conception.

Viewing the evidence in the light most favorable to the defendants as the verdict winners,9 we conclude that there was sufficient evidence to support the jury’s determination that Hardy was a co-inventor. To get there, the jury had to find that Hardy had made a significant contribution to the invention. Indeed, a reasonable jury could have concluded that both Mullan and Hardy had collaborated to discover the Swedish mutation. That Hardy was not present at the time and place when the identity and location of the mutation was confirmed does not mean he was not a co-inventor. There was abundant evidence that he and Mullan had been working together on the project to identify the Swedish mutation before and at the time of conception.

Evidence supporting the jury’s finding that Hardy was a co-inventor was provided by not only Hardy, but by others involved in the process. Hardy’s testimony was also corroborated by contemporaneous documents.

[746]*746Hardy, after obtaining the DNA and pedigrees for families 139 and 144 from Dr. Lannfelt,10 decided to conduct molecular genetic studies on those families.11

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Bluebook (online)
952 F. Supp. 2d 740, 85 Fed. R. Serv. 3d 1299, 2013 WL 3305743, 2013 U.S. Dist. LEXIS 91795, Counsel Stack Legal Research, https://law.counselstack.com/opinion/alzheimers-institute-of-america-inc-v-avid-radiopharmaceuticals-paed-2013.