Supreme Court Remands In Myriad Appeal

Today, as predicted by many commentators, the Supreme Court set aside the ruling by the Fed. Cir. that claims to isolated DNA sequences that are the BRCA 1 or 2 gene, or fragments thereof, are patentable subject matter. The Supreme Court ordered the Fed. Cir. to reconsider its 2-1 panel decision in view of its recent opinion in Prometheus that assays to optimizing drug efficacy based on measuring metabolite levels were no more than attempts to patent natural phenomena.

It is not entirely clear what guidance the Prometheus opinion provides for the appealed DNA claims in the Myriad decision. After all, the claims closest to the invalidated Prometheus claims were the claims to a method of locating mutations in a subject’s BRCA DNA by comparing it to a benchmark, or wild-type BRCA sequence. In the Supreme Court’s opinion, Justice Breyer contrasted the claims at issue with claims to a new compound:

 “Unlike, say, a typical patent on a new drug or a new way of using an existing drug, the [Promethus claims] do not confine their reach to particular applications of those  [natural laws].”

To invalidate claims to isolated DNA sequences, the Fed. Cir. and the Supreme Court would have to specifically interpret Chakrabarty to require that, to be “new” under section 101, a compound must exhibit a utility not possessed by the compound pre-isolation, even if the compound pre-isolation is structurally different than the compound post-isolation.  If the Fed. Cir. were simply to rely on In re Bergy, as I and others have suggested in previous posts on Myriad, it is difficult to imagine the Fed. Cir. reversing itself on this issue.

Even if gold in a streambed is not different from gold in a Krugerrand, isolated DNA in a “test tube”  is different from a DNA sequence that is one part of chromosomal DNA. However, the Supreme Court just added a “something more” requirement to a claim to optimizing a drug regimen, and the Court may be poised to put a “something more” requirement on a structurally novel chemical compound. I just hope that if the judges or justices go down this path, and hold that isolated DNA is a “natural product,”  they give us some hint of how to meet the “something more” requirement, going forward. They might also consider what “going forward” means.

Posted in Patent Eligible Subject Matter | Tagged , , , , , , , , , , , , | 1 Comment

“Handbook of Quality Procedures Before the EPO”

The ECP, epi and Business Europe have collaborated to produce a downloadable, fifty page guide to practice before the EPO. While not binding on Examiners, it was issued under the authority of the EPO and is a sort of mini-MPEP, intended for use by both applicants and Examiners. A copy is provided at the end of this post. You can read more about it here.

Handbook_of_quality_procedures_before_EPO_en

Posted in EP and UK Practice | Tagged , , , , , , , , | Leave a comment

PTO To Biotech Examiners – We’ll Get Back To You!

On March 21, 2012, Andrew H Hirschfield, Associate Commissioner for Patent Examination Policy, sent a short memo to the Patent Examining Corps to inform them about the decision in Prometheus v. Mayo. The “preliminary guidance” that was provided included a statement that mainly this decision did not affect the PTO’s Bilski guidelines re patenting “abstract ideas” (so keep calm software/business method Groups).

The memo described the unpatentable laws of nature at issue as “the relationships between concentrations of certain metabolites in the blood and the likelihood that a thiopurine drug dosage with prove ineffective or cause harm.” The memo noted that “the claimed processes [the “invention as a whole”] are likewise not patent eligible unless they have additional features that provide practical assurance that the processes are genuine applications of these laws rather than drafting efforts designed to monopolize the correlations. [The Court found that] the additional steps in the claimed processes here are not themselves natural laws, but neither are they sufficient to transform the nature of the claims.”

Continue reading

Posted in Patent Eligible Subject Matter | Tagged , , , , , | Leave a comment

Unnatural Acts – Patenting Diagnostic Tests Post-Prometheus

The US Supreme Court case of Mayo v. Prometheus has generated a lot of interest precisely because it clouds the future of patent claims to diagnostic methodologies in general and to ‘personalized medicine’ in specific. The decision is likely to make it very difficult to obtain claims to predictive diagnostic methods that depend on the presence or absence of a marker (such as a protein expressed by a certain gene that, say, is indicative of a propensity to develop cancer if the marker is present) and on diagnostic methods that compare the level of a biomarker to a benchmark “normal” or “abnormal” level of the marker (like the PSA assay for prostate cancer). The claims in Prometheus were closest to the second type – the marker is the metabolite level in the patient’s blood – even though it arose due to administration of a known drug and not endogenously – like an activated gene product.

This is because the Prometheus decision states that simply discovering and claiming such indicative correlations  (If “a”, then “b”) is an impermissible attempt to claim (and thus to monopolize) a natural phenomenon, or law of nature, unless the claim contains other feature that add something beyond a statement of the correlation. However, the Court gives no guidance in the area of medical diagnostics as to what that extra something should be. The Court simply denigrates and disregards the other steps present in the claim –  administering the reference drug, measuring the levels of its metabolites and drawing a conclusion about appropriate dosing from the levels that are measured.:

“In particular, the steps in the claimed processes [in Prometheus’s patents) (apart from the natural laws themselves) involve well-understood, routine, conventional activity previously engaged in by researchers in the field…upholding the patents would risk disproportionately tying up the use of the underlying natural laws, inhibiting their use in the making of further discoveries.” Slip op at 4.

“[D]o the patent claims add enough to their statements of the correlations to allow the processes they describe to qualify as patent-eligible processes the apply natural laws?”

Of course, the Court said that the answer was “No”. However, the Court provides no guidance as to what that “enough” might be, except to discuss the facts of three older decisions that have nothing to do with modern medicine.

Continue reading

Posted in Patent Eligible Subject Matter | Tagged , , , | 1 Comment