Find below biotech IP newsletters recently provided by Dr. Stefan Danner.
Find below biotech IP newsletters recently provided by Dr. Stefan Danner.
Course Announcement:
Intensive Patent Law Training Seminar
February 22-24, 2012
New York City
The Chisum Patent Academy is pleased to accept registrations for our next seminar, to be held on February 22-24, 2012 in New York City. Our venue is the American Elm conference room (Suite 503) of the Helmsley Park Lane Hotel, 36 Central Park South, New York, NY.
The three-day seminar will focus on recent and important legislative and case law developments in U.S. patent law, including the American Invents Act of 2011, post-KSR nonobviousness decisions, Therasense and the future of inequitable conduct, and the Federal Circuit’s ongoing schism over patent claim construction. Eighteen hours of CLE credit (including one hour of ethics credit) have been applied for. The registration fee is $2,750 per person.
A maximum of ten registrations will be accepted for this uniquely interactive round-table seminar. All sessions are co-taught by patent law authors and educators Donald Chisum and Janice Mueller. To register, please visit our website at www.chisumpatentacademy.com or email us at info@chisum.com.
By Paul Cole, European Patent Attorney, Lucas & Co – Warlingham, UK
Judgement – Human Genome Sciences Inc (Appellant) v Eli Lilly
and Company (Respondent)
The above proceedings relate to European Patent (UK) 0,939,804 concerning a new human protein called Neutrokine-α. The specification explained (i) the existence and amino acid sequence of Neutrokine-α, (ii) the nucleotide sequence of the gene encoding for Neutrokine-α, (iii) the tissue distribution of Neutrokine-α, (iv) the expression of Neutrokine-α by its mRNA (the encoding gene) in T-cell and B-cell lymphomas, and (v) that Neutrokine-α is a member of the TNF ligand superfamily. The specification described the invention as potentially useful for the diagnosis, prevention, or treatment of a large number of disorders of the immune system, either through Neutrokine-α itself or through its antagonists. However, nowhere in the Patent was there any data or any suggestion of in vitro or in vivo studies, so there was no experimental evidence to support any of those suggestions.
It took me a while to get around to reading Prometheus’s brief to the Supreme Court in Mayo v. Prometheus Labs., No. 10-1150 (S. Ct. Oct. 31, 2011), because I was pretty sure how it would read and, in fact, there are no major surprises. Prometheus argues that their claims must be considered as a whole, and that section 101 does not categorically exclude processes that end by providing useful information – what I called a “thinking step” in an earlier post. Prometheus argues that “Mayo’s categorical rule that all claims must end with an action step would just multiply byzantine claim drafting…This Court has routinely recognized that patents can properly leave ample room for ‘the judgment of the operator.” Res. Brief at 35. Prometheus also reaches into the Bilski opinion for one of the few helpful quotations: “Nothing in Bilski was intended to ‘create uncertainty as to the patentability of …advanced diagnostic medicine techniques.’ [130 S. Ct. at 3227[ let alone all processes provided valuable information.” Res. brief at 36.
Prometheus also takes the reader along the well-worn path of Morse, Benson, Flook and Grams to argue that the monitoring patents do not preempt all practical use of any “relevant principle” but then neatly circles back to Tilghman, 102 U.S. at 709, to argue that the patent in question “wholly preempted the ‘natural phenomenon’ that water applied at high temperature and pressure would have the stated effect on fatty bodies. But it did not preempt the broader natural principle that high temperature and pressure tend to break chemical bonds, and it did not preclude the use of other methods to separate fat acids and glycerine from fatty bodies, such as sulfuric acid distillation or steam distillation.”