United States of America

Bowman v. Monsanto Co. Et Al. (Supreme Court of the United States, 13 May 2013)

The United States Supreme Court decided that the use by a purchaser of self-replicating soybeans for planting purposes amounts to a reproduction of new soybeans and is therefore not covered by patent exhaustion.

Madey v. Duke University, 307 F.3d 1351 (Fed. Cir. 2002)

The Court of Appeals for the Federal Circuit interpreted the US experimental use exception in a very restrictive way. Regardless of whether a particular institution or entity is engaged in an endeavour for commercial gain, so long as the act is in furtherance of the alleged infringer's legitimate business and is not solely for amusement, to satisfy idle curiosity, or for strictly philosophical inquiry, the act does not qualify for the experimental use defense.

Case Summary

Eli Lilly & Co. v. Medtronic, Inc. - 496 U.S. 661 (1990) (United States Supreme Court)

The Supreme Court held that the scope of the regulatory review exemption covers the use of patented inventions reasonably related to the development and submission of information needed to obtain marketing approval of medical devices under the Federal Food, Drug, and Cosmetic Act.

CoreValve Inc v Edwards Lifesciences AG & Anor. EWHC 6 (Pat) (2009) (In the High Court of Justice, Patent Court, London)

It was held that the mere fact that the purpose of a use is commercial is no rebuttal of the statutory defence of experimental use. A more complete consideration of the defence requires consideration whether the immediate purpose of the transaction in question is to generate revenue. There is a need to consider the defendant's preponderant purposes.

Case Summary

Amgen Inc. v. Chugai Pharmaceutical Co. (US District Court, District of Massachusetts - 706 F. Supp. 94 1989)

The Court ruled that the export/import of samples of a biological product protected by patent for the conduct of stability studies "solely for uses reasonably related to the development and submission of information under" reporting requirements of federal drug laws, is permitted under the regulatory review exemption.

Roche Products Inc. v. Bolar Pharmaceutical Co., 733 F.2d 858 (Fed. Cir. 04/23/1984)

The Court of Appeals for the Federal Circuit (CAFC) ruled that the experimental use exception in US patent law is truly narrow. Where the subject matter of a patent is made or used as an experiment, whether for the gratification of scientific tastes, or for curiosity, or for amusement, the interests of the patentee are not antagonized, the sole effect being of an intellectual character in the promotion of the employer's knowledge or the relaxation afforded to his mind.

Case Summary

Spectra-Physics, Inc. v. Coherent, Inc., 827 F. 2d 1524 (Fed. Circ. 1987) US Court of Appeals for the Federal Circuit

This case addresses the distinction between the requirements to disclose an invention to the public in general terms (enablement) and the separate requirement to disclose the best mode of carrying out the invention. The district court found the patents at issue invalid due to lack of enablement. The United States Court of Appeals affirmed the judgment of the district court, but on different legal grounds, i.e. due to the failure to disclose the best mode of practicing the invention.

Dewey & Almy Chemical Co. v. Mimex Co., Inc., 124 F 2d 986 (1942) (U.S. Court of Appeals for the Second Circuit)

The United States Court of Appeals for the Second Circuit held that a prior art to be an anticipation must bear within its four corners adequate directions for the practice of the patent. If the earlier disclosure offers no more than a starting point for further experiments, if its teaching will sometimes succeed and sometimes fail, if it does not inform the art without more how to practice the new invention, it has not correspondingly enriched the store of common knowledge, and it is not an anticipation.

Amgen Inc., v. Chugai Pharmaceutical Co., Ltd., and Genetics Institute, Inc. (U.S. Court of Appeals - 927 F.2d 1200, Fed. Cir. 1991)

The the Court of Appeals for the Federal Circuit held that for the patenting of microorganisms the best mode disclosure requirement does not necessarily entail an obligation by the patent applicant to deposit a sample of the claimed microorganism.