Duramed Pharmaceuticals, Inc. v. Watson Laboratories, Inc.

413 F. App'x 289
CourtCourt of Appeals for the Federal Circuit
DecidedMarch 25, 2011
Docket2010-1331
StatusUnpublished
Cited by5 cases

This text of 413 F. App'x 289 (Duramed Pharmaceuticals, Inc. v. Watson Laboratories, Inc.) 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
Duramed Pharmaceuticals, Inc. v. Watson Laboratories, Inc., 413 F. App'x 289 (Fed. Cir. 2011).

Opinion

LOURIE, Circuit Judge.

Watson Laboratories, Inc. (“Watson”) appeals from the decision of the United States District Court for the District of Nevada, holding on summary judgment that the asserted claims of U.S. Patent 7,320,969 (“the '969 patent”) were not invalid for obviousness. Duramed Pharms., Inc. v. Watson Labs., Inc., 701 F.Supp.2d 1163, 1167-71 (D.Nev.2010). Watson also appeals the district court’s exclusion of its expert’s testimony on prior use of the claimed invention. Id. at 1166-67. Because the district court erred in its determination of nonobviousness, but did not abuse its discretion in excluding certain expert testimony, we reverse in part, affirm in part, and remand.

*291 Background

Duramed Pharmaceuticals, Inc. (“Duramed”) owns the '969 patent, which covers an extended-cycle combined oral contraceptive (“COC”) regimen commercialized by Duramed as Seasonique ®. Unlike traditional 28-day COC regimens, in which estrogen- and progestin-containing pills are administered for 21 days and hormone-free pills for 7 days, extended-cycle regimens increase the menstrual cycle’s natural length by administering hormone-containing pills for greater than 21 days. Extended-cycle regimens thus postpone estrogen-withdrawal symptoms experienced by many women during the hormone-free period. The incidence of estrogen-withdrawal symptoms can also be reduced by administering low dosages of estrogen during the traditional hormone-free period. Duramed’s Seasonique® combines an extended-cycle COC regimen with the administration of low-dose, unopposed estrogen during the hormone-free period. Specifically, the regimen consists of 84 daily pills containing 30 jig of the estrogen ethinyl estradiol and 150 jig of the progestin levonorgestrel, followed by 7 daily pills containing 10 jig of ethinyl estradiol only.

On March 6, 2008, Duramed brought suit against Watson under 35 U.S.C. § 271(e)(2) after Watson filed an Abbreviated New Drug Application (“ANDA”) seeking Food and Drug Administration (“FDA”) approval for a generic version of Seasonique®. Duramed alleged infringement of claims 1-9, 15, and 17-19 of the '969 patent. Claim 19 is representative:

19. A method of contraception in a female in need thereof the method comprising administering to the female a dosage comprising a combination of estrogen and progestin for a period of 84 consecutive days, followed by administration of a dosage consisting essentially of estrogen for a period of 7 consecutive days,
wherein the estrogen that is administered in combination with progestin for the period of 84 consecutive days is orally administered monophasicly in a daily amount of about 30 jig of ethinyl estradiol,
the estrogen that is administered for the period of 7 consecutive days is orally administered monophasicly in a daily amount of about 10 jig of ethinyl estradiol, and
the progestin that is administered in combination with estrogen for the period of 84 consecutive days is orally administered monophasicly in a daily amount of about 150 jig of levonorgestrel.
'969 patent claim 19. The '969 patent issued on January 22, 2008, and claims priority back to an application filed on December 5, 2001.

Watson stipulated to infringement but challenged the '969 patent’s validity under 35 U.S.C. § 103. In making its obviousness challenge, Watson relied on, inter alia, (1) a 1994 Kovaes article, which describes an extended-cycle COC regimen of 84 daily pills containing 30 jig ethinyl estradiol and 150 jig levonorgestrel, followed by 7 daily hormone-free pills; (2) U.S. Patent 6,027,749 (“the '749 patent”), which discloses COC regimens of up to 77 daily pills containing 15-20 jig ethinyl estradiol and 50-125 jig levonorgestrel, followed by 7 daily pills containing 10-15 jig ethinyl estradiol to reduce the incidence of premenstrual headaches; and (3) two Sulak articles from 1997 and 2000, which describe the problem of headaches resulting from estrogen withdrawal as well as the use of low-dose, estrogen-only pills during the hormone-free period as a way to alleviate such headaches.

*292 Watson’s expert witness, Dr. Michael A. Thomas, opined on the teachings of these prior art references. He also opined that one of skill in the art would have been motivated to combine the Kovacs COC regimen with the 7 days of unopposed estrogen as claimed in the '969 patent because the Kovacs article recognized that the regimen may result in headaches in some women. J.A. 824-25. In addition, Dr. Thomas testified that he had personally prescribed the contraceptive regimen claimed in the '969 patent prior to the patent’s priority date, December 5, 2001. The district court granted Duramed’s motion to exclude Thomas’s testimony regarding this prior use as uncorroborated. Duramed, 701 F.Supp.2d at 1166-67.

The district court also granted summary judgment of nonobviousness. The court analyzed Watson’s “three most significant” prior art references, the Kovacs article, the Sulak article, 1 and the '749 patent, finding the remaining art “cumulative.” Id. at 1168 n. 3. Regarding the Kovacs article, the court found that it did not provide support for combining 84 daily hormone pills with 7 days of unopposed estrogen to alleviate estrogen-withdrawal symptoms because it describes headaches throughout the menstrual cycle and fails to make any mention of using unopposed estrogen. Id. at 1168-69. Regarding the Sulak articles, the court found that, although they identify headaches as a symptom of hormone withdrawal, they mention the addition of unopposed estrogen only as a theoretical, untested solution. Id. at 1169-70. Regarding the '749 patent, the court found that by disclosing a variety of COC regimens, the patent did not establish consistent knowledge in the community, and that it pz'ovided no basis for adding estrogen-only pills to the end of a COC regimen to alleviate withdrawal headaches. Id. at 1170. Finally, the court found that Watson’s expert, Thomas, was not a person of ordinary skill in the art, but rather an active pai'ticipant in research in the field of endocrinology. Id.

Watson appealed. We have jurisdiction pursuant to 28 U.S.C. § 1295(a)(1).

Discussion

This court reviews a distiict court’s decision on summary judgment de novo, reapplying the same standard applied by the district court. Iovate Health Scis., Inc. v. Bio-Engineered Supplements & Nutrition, Inc., 586 F.3d 1376, 1380 (Fed.Cir. 2009). Summary judgment is appropriate only “if the movant shows that there is no genuine dispute as to any material fact and the movant is entitled to judgment as a matter of law.” Fed.R.Civ.P.

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413 F. App'x 289, Counsel Stack Legal Research, https://law.counselstack.com/opinion/duramed-pharmaceuticals-inc-v-watson-laboratories-inc-cafc-2011.