PTO Biotech/Chem/Pharma Customer Partnership Meeting Announced

The USPTO has announced that it will hold a meeting of the Biotechnology/Chemical/Pharmaceutical Customer Partnership on Tuesday, March 2nd, in the Madison Auditorium of the USPTO in Alexandria, VA (agenda attached). You can attend in person or via a link to join online. In the past, I have been less than enthusiastic about these events. From their start in the 90’s, they devolved from small meetings of representatives of IP law user groups with senior Examiners (I met John Doll at one of these meetings) to try to resolve differences in examination policy (e.g., what does per cent sequence identity mean?) to one-day conferences which were mostly consumed by the PTO telling us how great they were (or planned to be in the near future). But this agenda looks like it has some meat on the bones. Topics include reissue, PTA, accelerated examination and synthetic biology. Time to give it another try.

BCP 030210 Agenda Updated

Accessing the event:

1.    Double click on the link below (or copy it into your internet browser)https://uspto.connectsolutions.com/r45099374/

2.    Select the “Enter as a Guest” option.

3.    External guests – please login using your email address

USPTO Employees – please login using your last name, first name

4.    Click on the “Enter Room” button

5.    You will be admitted to the meeting

Assistance

If you need assistance with login, please contact Darcy Bates at (571) 272-2499 or Carrie Scott at  (571) 272-2992.

 

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ANOTHER “HAIL MARY” CLAIM BITES THE DUST

In my post of April 22, 2009, I spent quite a lot of time discussing why “mechanism of action” claims may issue but, like the “Hail Mary” pass in football, remain vulnerable to invalidation as inherently anticipated by the prior art, taken with discoveries made long after the filing date of the claims. Much of this discussion was in the context of the reexamination of the NF-kB patent claims asserted by Ariad against Lilly. I posited that the PTO had effectively taken the position, with respect to such claims, that:

 (A) Method claims whose only recited steps are altering biological mechanisms of action are invalid as anticipated, under principles of inherency, by a prior use of a biologically active compound that meets two requirements:

1.  More than a year prior to the effective filing date of the claim at issue, an “old compound” was administered, so as to treat a condition or achieve a result encompassed by the condition or result recited by the claim at issue; and

2.  At any time, it is shown that the mechanism of action of the “old compound,” when used to treat the condition or achieve the result, is the mechanism of action recited in the claim.

 In the Ariad reexamination, at one point, the PTO Examiner cited the Old Testament of the Bible against the claims, in combination with a recent publication that demonstrated that reservatrol, a compound present in red wine, inhibited the NF-kB pathway. Thus, Bible stories in which red wine was consumed inherently anticipated claims to a method of inhibiting NF-kB activity in a cell by contacting the cell with an NF-kB inhibitor (some of the claims at issue in the patent asserted by Ariad were even broader than this).

This principle was applied by the Board on February 12, 2010, again in Lilly’s favor, to invalidate claim 24 of Pfizer’s Viagra patent (U.S. Pat. No. 6469012):

Claim 24. A method of treating erectile dysfunction in a male human, comprising orally administering … an effective amount of a selective cGMP PDEv inhibitor, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing either entity. (Ex parte Pfizer, Appeal No. 2009-004106, Bd. App. Feb. 12, 2010).

Pfizer had sued Lilly for infringing claim 24 by selling Cialis, admittedly a PDEv inhibitor. Lilly requested reexamination and urged that claim 24 was invalid as inherently anticipated by a (I assume “ancient”- as it is described in Chinese Herbal Medicine Materia Medica)  treatment for impotence involving inter alia, drinking rice wine and imbibing an herb whose Latin name translates as “horny goat weed,” in combination with later evidence that demonstrated that the herb in fact contained icariin, a selective cGMP PDEv inhibitor, that would be effective to treat ED when administered in regimens disclosed in the Chinese literature. The Board found the evidence convincing, and affirmed the Examiner’s invalidation of the claim.

So the next time a professor-client or tech transfer person wants you to write this sort of claim, based on a newly discovered mechanism of action, remember that, like the Hail Mary pass,  you can put it up there, but it might not stay up for long.

You can read more about it at Law36o.

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PTO “POINT SYSTEM” DISTRIBUTED

I thought it worthwhile to post this “point system,” since I had never seen one before. It is encouraging that the highest tier of points an Examiner can achieve is a first office action allowance, but a little discouraging that “Qualifying” an application in the first action and giving it a first office action final rejection are weighed equally. But notice the goodly number of points the second (or subsequent) Examiner gets for allowing the application. Also, there must be some other sort of credit for participating in an interview, right? Right?

 PAP addendum 2-14-10

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Novelty and Obviousness In An Empirical Research Field – The Decision of the UK Court of Appeal in Dr Reddy’s Laboratories v Eli Lilly

From Paul Cole

The Lilly patent for olanzapine has been litigated in many jurisdictions including the US, Canada, the Czech Republic, Finland,

Romania, Slovakia, Slovenia, Spain, China and Hungary. In US Court of Appeals for the Federal Circuit in Eli Lilly v Zenith Goldline (26 December 2006) Judge Rader held that allegations of lack of novelty and of obviousness did not succeed, whereas in the Canadian decision in Eli Lilly Canada v Novopharm (5 October 2009) O’Reilly J. held that the patent did not meet the requirements for a selection patent and was invalid. Key issues before the UK Court of Appeal were how novelty and obviousness of a secondary patent in the pharmaceutical field should be evaluated, the extent to which decisions of courts within the UK prior to the introduction of a “new law of patents” in 1977 remained relevant, and in particular whether the reasoning in the Canadian decision should be followed. The members of the court included Lord Neuberger in his capacity as Master of the Rolls and Sir Robin Jacob, both very experienced in handling pharmaceutical patent disputes.

Their decision confirms the extent to which, at least in this field, the law in the UK has departed from relatively restrictive pre-1977 standards and has become aligned with more open decisions of the EPO Appeal Boards. It also shows that in future there will be scope for differences between decisions of the UK courts following the “new” post-1977 law and those in e.g. Canada, India, Australia and New Zealand where the link to the older common law remains unbroken.

The Court of Appeal refused to hold that disclosure of a class was disclosure of all members of that class, relying on a quotation from G. K Chesterton’s Father Brown story “The Sign of the Broken Sword: “Where does a wise man hide a leaf? In a forest?” Accordingly the invention as claimed was novel. And even though prior art disclosures included ethyl olanzepine which differed from the claimed compound in only a single carbon atom, the court refused to hold that an objection of lack of inventive step had been established.

The decision includes scathing comments on a prior art reference with a Markush claim allegedly covering some 10-to-the-19th compounds. The court observed that all the skilled reader would get from that reference was a vague promise of neuroleptic, sedative or relaxant effect for all the 10-to-the-19th compounds with an equally vague promise of high therapeutic index coupled with no evidence to support these promises. Given that the whole field was unpredictable, the woolly teaching of the reference (described by Lord Neuberger as “mere speculation”), if not totally useless, was no guide to any particular compound. It could not be said that any compound out of a vast class was obvious if there was no real idea how any individual member of that class might behave.

Yet further confirmation has been given to the realistic approach of UK courts to inventions in empirical research fields, and to the supportive judicial attitude towards the research-based pharmaceutical industry as also demonstrated by Sir Robin’s speech on 29 November 2008 to the EU Directorate-General of Competition at the time of their preliminary report on their Phrma-sector enquiry, see Patents and Pharmaceuticals

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