US Judge Voids Gene Patent

April 1, 2010

Judge Robert W. Sweet  of the U.S. District Court has invalidated patents related to the BRCA1 and BRCA2 genes that are held by Myriad Genetics. In addressing the issue of whether isolated human genes and the comparison of their sequences are patentable,  The 88-year-old Judge Sweet has ruled that the patents lacked novelty since genes are part of nature.

The Plaintiffs included the American Civil Liberties Union on behalf of women’s health groups, geneticists and scientific associations representing approximately 150,000 researchers, pathologists, laboratory professionals and individuals diagnosed with breast cancer, challenged patents held by Myriad Genetics and the University of Utah Research Foundation on grounds that genes are “products of nature and cannot be patented.” They were represented by the ACLU  and by the Public Patent Foundation of the Cardozo School of Law, Yeshiva University.  The plaintiffs managed to invalidate seven patents related to the human BRCA1 and BRCA2 genes, which indicate susceptibility to Breast Cancer.

The United States Patent Office has a long-established practice of granting patents on DNA sequences in the form of “isolated DNA,” with some 17,000 gene patents issued and over 30,000 applied for. Unlike business method patents and methods of therapeutic treatment which are both patentable in the US only, other countries also see genes as legitimate patentable material. 

The District Court ruled in favor of the Plaintiffs, granting summary judgment and reasoning that the patent claims covered “products of nature, laws of nature and/or natural phenomena, and abstract ideas or basic human knowledge or thought.”
 
Judge Sweet reasoned that DNA is a physical embodiment of biological information, and is distinct from any other chemical found in nature.  Isolating DNA neither alters its fundamental quality, nor does it alter the information that DNA encodes.  Since the patents are directed to sequences found in nature, they are unpatentable subject matter.  
 
This ruling is not binding on other federal courts, and does not apply to other types of patents. However, we exect the case to be appealed to the Court of Appeals for the Federal Circuit, and it may ultimately go to the Supreme Court.

The argument centers round whether isolating a gene sequence is discovery or classification, or is it inventing. Philosophically, I would tend to go with the honorable judge and consider there to be a lack of novelty, or, at least a lack of inventive step in patents for gene sequences. Nevertheless, as with pharmaceutical patents, being able to monetize gene research requires being able to obtain ownership over them, which requires them to be considered patentable inventions. Without patent protection being available, there may not be the resources available for doing genetic research.

The first Patent Act of the U.S. Congress, entitled “An Act to promote the progress of useful Arts”, was passed on April 10, 1790. It legislated for the grant of a patent to an inventor fulfilling the appropriate formalities “if they shall deem the invention or discovery sufficiently useful and important”. Thus from the very earliest days in the US, patents discoveries were considered patentable if useful. 

In re Bergy, the Court of Customs and Patent Appeals (the predecessor of the modern Federal Circuit) upheld a patent directed toward a purified version of an antibiotic producing strain of streptomycin, a substance that appears in nature in an unpurified state.  In Chakrabarty, the Supreme Court held that genetically modified micro-organisms not found in nature can be patented.  The Supreme Court also held in J.E.M that newly-developed plant breeds are patentable.  The Supreme Court has not, however, specifically considered the patentability of human genes.
 
Nevertheless, the patents covering the BRCA1 and BRCA2 genes are not unusual or unique. The United States Patent Office has been granting patents for chemical compositions based upon human extractions for over 100 years. The first patent for such a chemical was granted in 1907 for adrenaline. Insulin was patented in 1923.

Neither chemical and certainly no gene string occurs naturally in isolation. Those favoring patentability argue that the extraction and characterization is essentially inventing. In terms of genetics, inventors must:
(1) identify novel genetic sequences
(2) specify the sequence’s product
(3) specify how the product functions in nature –ie, its use
(4) enable one skilled in the field to use the sequence for its stated purpose

By linking the utility requirement to use, the argument that the invention is not novel and is naturally occurring substance is emphasized.
In the US, the Patent Office currently interprets Chakrabarty as allowing the patenting of living things, regardless of whether they are genetically modified (Chakrabarty) or isolated and purified by man (Bergy).  Further, the Patent Office takes the position that genes are treated as chemical compounds and qualify for potential patenting as compositions of matter. 

It should be noted that the claims challenged in the Breast Cancer Susceptibility Gene patents include two types: (1) composition claims, and (2) method/process claims.  The first set of claims was invalid as a “product of nature,” and the second set of claims was invalid as representing an abstract idea. There were also claims to a kit for diagnosis and to a probe. Such claims were not challenged.

The case: Association for Molecular Pathology et al. v. United States Patent and Trademark Office et al., No. 09-Civ-4515 (S.D.N.Y.)

Researchers at Duke University  analyzed U.S. Patent No. 5,747,282 and compared a 15-mer oligonucleotide in the BRCA1 gene described by one of the patent’s claims against gene sequences in GenBank, the NIH genetic sequence database. They found that 80% of cDNA and mRNA in the database contain at least one oligonucleotide covered by the claim.

The researchers conclude that any ‘isolated’ DNA molecules that include such 15bp nucleotide sequences would fall under the claim as granted by the U.S. Patent and Trademark Office (USPTO). Thus, some 300,000 oligonucleotides in chromosome 1, which does not contain the BRCA1 gene, are, nevertheless, covered by the claim, and anyone making, using, selling, or importing such a molecule for any purpose within the United States would thus be infringing the claim.

As with the infamous Pfizer patent for Viagra which covers very many molecules not known to be active, it seems that gene patents, like pharmaceutical patents, tend to be too broad. Such patents are filed for early on during research, prior to a deep understanding of what aspects are commercially valuable.

Time will tell how this controversial ruling by a man in his late eighties will stand up to Appeal. In the meantime, there is a lot of research money and patent activity that will go on hold.   

Gene Patents in Israel

Back in October 2008, in Circular M.N. 64, the Israel Commissioner of Patents announced that gene sequences can now be patented in Israel. See Gene Sequences are now patentable in Israel. However, that ruling ignored the fundamental issue of whether such things are fairly described as being inventions and is also probably ultra-vires. So if challenged in Court, a judge could over-rule the Commissioner.

Gene Patents elsewhere

The same issue is being considered in Australia, see Gene Patents Under Attack and the European Court of Justice has also been asked to clarify through interpretation of Directive 98/44 whether a DNA sequence is entitled to patent protection as a compound as such, or only under circumstances where the DNA performs its function.

For an interesting rave by Gene Quinn, see Hakuna Matada, the ACLU Gene Patent Victory Will Be Short Lived.


Teva comes to agreement with Barr and Schering Regarding Temodar

March 21, 2010

Temodar® is an anti-cancer chemotherapy drug used for treatment of anaplastic astrocytoma and glioblastoma multiforme (GBM) brain tumors. The drug was patented by Schering and is known generically as temozolomide.

Teva have announced that the parties to the patent litigation regarding Barr’s U.S. generic version of Schering’s Temodar(R) have entered into an agreement pending resolution of Schering’s appeal to the Federal Circuit of the U.S. District Court’s decision holding the ’291 Patent unenforceable. Under the terms of the agreement, subject to limited exceptions, Teva will only market a generic product should the Federal Circuit uphold the District Court’s decision. Furthermore, the agreement grants Teva the right to commence selling its generic product as of August 2013, during the period of Schering’s pediatric exclusivity.


The International Patents and Trademarks Database ands similar scams!

March 21, 2010

As the agent of record, I have just received three invitations, on behalf of separate clients, to register their details in the International Patents and Trademark Database. It is my considered professional opinion that the benefit derived from so doing is totally outweighed by the charge of $US 2717.

Were I to report this invitation to my clients, I would advise them not to take advantage of the offer. Do any readers consider that I have any fiduciary, assumed contractual or other obligation to report the invitation to them? Can I simply bin it on my own initiative?

For an official WIPO list of similar scams – see http://www.wipo.int/pct/en/warning/pct_warning.htm


Wyeth Accuses Teva of Widening Grounds of Opposition, but Israel Patent Office Adjudicator, Refuses to Dismiss Claims in Interim Ruling

March 2, 2010

Teva are opposing Wyeth’s Patent Application Number 151450, which is a divisional application of 120382  “Extended Release Formulation Of Venlafaxine Hydrochloride”.

When Teva submitted 60 odd publications, Wyeth accused them of widening the basis of their opposition, claiming that the information should have been submitted in the Statement of Case. Additionally, they claim an interesting idea of Parent Application Estoppel, claiming that by not opposing the parent application, the opposer is estoppeled from opposing the divisional application, and requested the relevant clauses to be struck from the record.

Teva claim that the sixty publications submitted were indicative of the state of the art and were not substantive new grounds for opposition. Furthermore, Teva point out that Dexel have submitted these publications in parallel opposition proceedings. As to the Estoppel argument, Teva suggested that this should be discussed on its merits in the opposition proceedings.

Shoshani Caspi has refrained to comment on the issues raised and is allowing the new publications to be cited. She has, however,  required Teva to state what each publication contributes to establishing the State of the Art.

I think Shoshani Caspi’s position is reasonable. I am, however, at a loss as to what Wyeth, represented by Richard Luthi, have to gain by having prior art excluded from an opposition proceedings on procedural grounds. If  a patent were to issue due to prior art that negates novelty or inventive step not being considered on a technicality, presumably the patent would be unenforceable as it would not hold up in court.


Israel Court Rejects Request to Dismiss Charges for Copyright Infringement Concerning Screening UEFA Cup in Pizza Parlour

February 23, 2010

The UEFA Cup is a sports competition whose organizers licence screening rights to various bodies. One of the licensees, Charlton LTD, sued Pizza Pazza (2000) LTD. and the proprietor thereof, for illicit screening of match games in 2008.

The defendants attempted to have the case dismissed, based on the fact that the plaintiff did not cite UEFA as a co-plaintiff and did not provide all the documentation to show that they had screening rights.

The judge, Ms Abigail Cohen, dismissed the request to dismiss the case, pointing out that this was an extreme measure. Instead, she gave the plaintiffs an opportunity to correct their statement of case, and announced that she would rule on costs at the end of the trial. 

The decision seems to be a correct one. The decision is a significant one since 18 months ago, Judge Michal Agmon Gonen had requested government clarification when faced with a case concerning webcasting football matches, where she was unclear as to whether the 2007 Copyright Act changed the substantive Law from the Israel Supreme Court Decision in TeleEvent, see http://blog.ipfactor.co.il/2008/07/17/moving-copyright-goalposts/

We are thus pleased that the judge in this case considers public screening of matches as copyright infringement and is not prepared to dismiss the case on a technicality. 

We wonder however, why the defendants or the judge didn’t point out that IP Law is not within the jurisdiction of the Magistrate’s Court???

T.A. 14692-09-09 Charlton LTD vs. Pizza Pazza (2000) LTD. and others


Israel Commissioner Limits Possibility of Filing Divisional Applications to Lifetime of the Parent Application

February 18, 2010

 Section 24a of the Israel Patent Law 1967 allows for filing a divisional application at any time up to a patent application issuing.

In the interests of clarifying the scope of protection, in Circular 81, the Commissioner of patents has ‘clarified the ambiguity of’ this Section of the Law by interpreting it to mean that divisional applications can only be filed prior to the parent application issuing.

Comment

With the proposed amendment allowing for 18 month publication, this measure is clearly required. Nevertheless, I am not convinced that this is interpretation of the law, but rather amendment thereof.

Arguably this measure requires a formal amendment to the Law by the Knesset and goes beyond the authority of the Commissioner. It should be included in the proposed amendment for 18 month publication (second reading) and it would be fun if someone challenges this Circular on procedural grounds.


Israel Patent Office Appoints Ombudsman to Deal with Customer Complaints

January 25, 2010

 

In a welcome development,  the Israel Patent Office has announced establishing an ombudsman to deal with customer complaints. Dissatisfied parties can now email Patent.Customer-Serv@justice.gov.il.

I believe this development to be part of an ongoing initiative by the Israel Patent Office to obtain ISO certification, and view both developments positively. 

 


Israel Ministry of Justice Proposes Amendment to Patent Law

January 12, 2010

 Background

An anomaly of the Israel Patent Law is that applications do not publish automatically 18 months from the priority date. Instead, only the basic biographical information publishes shortly after filing, and the specification and claims publish for opposition purposes only, once allowed. Thus Israel has a submarine patent system as existed in the US prior to 1996, but as no longer exists with other important patenting jurisdictions.

Noting that frequently there is a corresponding PCT application or national application that publishes after 18 months, the Justice Ministry has published a document that hypothesizes that the current state of affairs enables competitors to learn an applicant’s technology and to implement it in Israel whilst still pending, thereby not providing grounds for the applicant to sue, and proposes an amendment to the Law.

The Proposed Amendment 

The proposed amendment provides for automatic publishing after 18 months and also provides for the applicant to obtain reasonable damages from infringing acts performed after publication and prior to allowance. It is not clear, but seems to be implied that to collect such a royalty, the allowed patents should be substantially as claimed in the patent application as published. The proposed amendment includes a further few provisions.

  1. The application should include an abstract that defines the scope of the invention.
  2. Under the (infamous) A.Sh.I.R. Decision, the District Court, upheld by the Supreme Court, has allowed compensation for ‘non-patented inventions’ under the Law of Unjust Enrichment. This is problematic as it is not clear whether inventors of such non-registered patents are entitled to protection if the invention is directed to subject matter not patentable under Israel law; for expired patents; for patentable subject matter not filed as a patent, or for inventions where due to prior publication by the inventor, there is no novelty. The amendment proposes scrapping unjust enrichment as grounds for legal action where a patent exists or where a patent was not filed.
  3. The publication fee will be canceled, possibly with an amendment to the filing fee.
  4. The file wrapper will available for inspection from this 18 month publication.

 Comments

  1. I see this as a welcome development. If and when passed, this amendment will conform the Israel patent practice to that of the rest of the world.
  2. In my opinion, simply conforming to the practice of the US, UK, EPO, Japan, PCT etc. is sufficient justification for the proposed amendment. The proposal suggests another reason – that the current system does not strike a current balance between the rights of the applicant and of third parties. It is a good point.
  3. Since November 2008, the Israel Patent Database of searched patents has been available for examination on-line. See Israel Patent Database Goes On-line. Technologically, therefore, it seems that the Israel Patent Office will be able to implement this reform if passed into Law.
  4. In February 2008, the Ministry of Justice turned to patent attorneys and other interested parties with a first draft and request for comments. See Israel Justice Ministry Drafting Amendment to Automatically Publish Applications 18 months After Filing
  5. There are, however, a couple of issues not appearing in the draft proposal.
    1.  Should automatic publication occur for all applications? or, as in the US for example, if an application is not filed abroad, will the applicant be able to request withholding of publication until the patent is allowed?
    2. Should third parties be allowed to submit prior art during examination? – This could provide a solution for one of the problems with allowing patents for software, i.e. the problem of searching for prior art.
  6. I am pleased that A.Sh.I.R. apparently to be conscribed to the scrap-heap of lousy Court decisions, but the wording is not clear. For example, only last week Judge Shapira granted a temporary injunction in a case involved challah cloths that were similar to those of another manufacturer. See Jerusalem Court Issues Temporary Injunction Against Copycat Challah Cover Manufacturers. I criticized granting temporary injunctions and referring to property rights where the plaintiff had not filed a design application. In Israel, design protection are covered by the original patent ordinance that was superseded - as far as patents are concerned – by the 1967 Patent Law. However, unlike the United States which grants design patents, in Israel, registered designs are not clearly a type of patent. The proposed amendment vis-a-vis A.Sh.I.R. might include designs or not. It is not clear, and the issue should be clearly related to.
  7. The arguments against A.Sh.I.R. are equally valid for designs as for patents. The precedent leaves too much to the discretion of the courts.
  8. There was a first reading of the a proposal for this amendment in 2005 or 2006, and implementation of Madrid has been stuck for quite a while, so we are not holding our breath as to when this proposed amendment will enter the Law. Unfortunately, the political and security situation in Israel is such that IP reform does not get the priority that I would like it to.

State of Israel Sues Omrix for NIS 500 million, Claiming Core Technology is Based on Service Inventions. Have They Killed the Golden Goose?

January 10, 2010

The State of Israel, represented by Dr. Shlomo Cohen & Co., Law Offices, has filed a NIS 500 million ($132 million) lawsuit in the Tel Aviv District Court against Omrix Biopharmaceuticals Ltd. and entrepreneur Robert Taub. Omrix, purchased by Johnson & Johnson in 2008 for $438 million, has commercialized a number of related inventions concerning medical adhesives for use in treating hemophiliacs and other applications. In the lawsuit the State claims that the company has stolen its Intellectual Property.

The State is basing its claims on testimony and documents submitted by state witness Prof. Uriel Martinowitz who they claim is the real inventor of Omrix’s patent portfolio.

This case, which is unprecedented in Israeli judicial history, is based on the following allegations:

  • Martinowitz is the true inventor.
  • In accordance with those sections of the Law regarding service inventions of security personnel and state employees, the inventions can fairly be considered belonging to the State, since when Prof. Martinowitz developed the inventions he worked in the IDF and subsequently in Sheba Hospital which is state-owned.
  •  Martinowitz could and should have reported the inventions to his employer, the IDF or the hospital management or perhaps the Ministry of Health, who could then have reached a fair arrangement with Dr. Martinowitz and Omrix.
  •  The legal opinions on which Omrix based its position that the inventions were not Service Inventions, were tailored to order, and therefore worthless.
  •  Fraud was committed when Omrix removed Martinowitz’ name from one of the earliest of the US patents, and when he was not listed as an inventor in subsequent patent applications.

Comments

A press release issued by the Justice Ministry on December 22, 2009 states, “the charges were filed in accordance with Government policy of protection and restoration to the State of Intellectual Property and Patents, and of dealing with the phenomenon of causing damage to State Property and the rule of Law.”

Not everyone agrees that this declared government policy is supported by the facts. In her book, The Capitalism of Knowledge, (Israel Ministry of Defense, 2008) Prof. Hagit Messer Yaron writes that the State has done little to create mechanisms for technology transfer. In fact, it is likely that had Prof. Martinowitz tried to work within the framework of Government bureaucracy, he might have hit a brick wall. And he would not have been alone.

In a lecture at a seminar co-hosted by JMB, Factor & Co., the Ono Academic College and WIPO in September 2009, Professor Messer Yaron reiterated this position and Dr. Yaron Zelikha, who, as Accountant General, had tried to set up a committee to further the issue, concurred with her.

AIDS Research

In 1996, Dr. Zeev Treinin, the director of the Veterinary Institute of the Ministry of Agriculture discovered / invented a promising treatment for AIDS. Acting properly, he did not file a patent application independently. He approached his employer who was not interested. Although no patent application was filed, the invention was published in an academic journal. This placed the technology in the public domain. Not surprisingly, no commercial drug developer was willing to invest the vast sums of money required to commercialize this AIDS treatment, as they would be defenseless against generic versions thereof.

Until filing the current case, the State has generally turned a blind eye to unauthorized patenting and commercialization of civil service inventions and has not set up mechanisms for patenting and technology transfer as exists in Israeli universities. Had Prof. Martinowitz acted properly and turned to his employers, it is questionable whether he would have been more successful than Dr. Treinin.

By way of example, while the Law sets out a mechanism for dealing with public sector inventors, the committee for determining appropriate royalties for service inventions never convenes. Similar treatment caused Sir Frank Whittle, the inventor of the jet engine, to emigrate from the UK to the USA, where he was appreciated.

The Statement of Case alleges that Prof. Martinowitz was involved in academic research. This may have been a costly error. In September 2009, in the case of the University of Western Australia v Gray, the Australian Full Federal Court upheld a decision that a medical doctor affiliated with both the university and a teaching hospital, behaved reasonably when he filed patent applications in his own name. The ruling established that academic researchers were not employed to invent, per se. In a similar decision, Leland Stanford Junior University vs. Roche, the US Court of Appeal Federal Circuit ruled that the faculty inventor Mark Holidniy owned rights in his invention for an HIV testing kit despite contractual obligations with the university and the Bay Dohl Act. It may be further argued that since 1980, the Basic Laws provide an additional basis for defense. Regardless of whether a doctor is a civil servant employed by a State hospital, one of the health funds (HMOs) or a trust-owned hospital, the job description is the same and similar rules should apply. Even if Prof. Martinowitz is established as the true inventor, the Courts may follow US and Australian precedents and decide that his inventions are his own.

Attorney Dr. Shlomit Yanisky Ravid was awarded a Ph.D. from the Hebrew University for her thesis on employee rights. She believes that Israel Patent Law regarding Service Inventions provides the courts with a great deal of leeway in interpretation. Although there may be evidence that Prof. Martinowitz did not behave correctly, the State has made a deal with him, so his culpability is moot. Instead, it is suing Omrix and its Managing Director Robert Taub.

A further problem in the case is that Prof. Martinowitz, is a state witness who has behaved improperly and has his own complaints against the defendants who owe him $750,000 promised but never paid. These facts undermine his credibility.

According to the Statement of Case, the defendants approached their IP Counsel, licensed both in Israel the US, for a legal opinion relating to the question of whether the inventions are Service Inventions. Counsel opined that Martinowitz’ early inventions were not Service Inventions since they were invented after his discharge from the IDF and while on leave. Furthermore, as counsel to Omrix, the same attorney determined that Prof. Martinowitz was not the inventor of the claimed invention that previously carried his name.

As Omrix actively involved legal counsel, the company may claim to have performed due diligence, presented the facts to a leading IP Lawyer, and thus did no wrong. An important question in this case may thus turn out to be whether the IP lawyer made sufficient effort to identify the inventors.

Even if only some of the allegations in the Statement of Case are correct, Omrix’ IP counsel may have some explaining to do. Particularly, as according to the Statement of Case, one of the early applications listed Prof. Martinowitz as an inventor when it was filed, but his name was subsequently removed. The Statement of Case asserts that claims allegedly directed to Prof. Martinowitz’ contribution were canceled in the US, justifying removing his name from the application. However, these claims were apparently restored on allowance without reinstating his name. While the patent attorney may be able to show that he was acting in good faith, it certainly raises the question as to the extent to which a patent attorney should be able to accept information at face value from a client, or whether there are some cases in which this is insufficient. Either way, the State, the defendants, and Johnson & Johnson may seek explanations as to exactly what happened.
Furthermore, since the Israel patent application has been abandoned, the defendants may argue that the Israel Court has no jurisdiction, and that the case should have been filed in the US.

Surprisingly, the State used the boutique IP Law firm that handles Johnson and Johnson’s large Israel trademark portfolio.

Although, precedents on various issues such as the obligations on researchers in the public sector may now be resolved, one wonders if this was the correct test case for the Government to bring.

Due to the strategy adopted by the State’s Counsel in the Statement of Case as filed, the charge of inventor fraud hangs like a cloud over Omrix’ patents and probably makes them unenforceable until the identity of the inventor(s) is resolved. However, in alleging fraud, State Counsel has established a basis for the USPTO to revoke the patents as being based on inventor fraud. If revoked, there will be no royalties and no market exclusivity. To reclaim its allegedly stolen property intact the State should have argued that a mistake was made in identifying the inventor. Mistakes can be corrected.

By adopting a questionable approach and by filing what seems to be a poorly constructed Statement of Claim, the State may have simply killed the golden goose, whereas by doing nothing, the State could have collected income from taxes, both income and corporate.

While this case will no doubt give State Employees pause for thought when it comes to the rule of law, establishing mechanisms for rewarding inventors in the public sector is equally imperative.


The Strange Affair of Israel Patent Application Nos. XXX and YYY to ZZZ

January 8, 2010

Under the Israel Patent Law there is a provision whereby sensitive patent applications affecting national security and the like must be first filed by Israeli inventors in Israel, and the patent office refers such applications to the Minister of Defense who have six months to decide whether to ‘classify’ the application and issue a gag order, preventing the application from being filed abroad or otherwise published.  If the Ministry of Defense does not issue such an order, the application may be filed abroad.

 

Whilst many applications of possible military significance are forwarded to the Ministry of Defense, it is fairly rare for applications to actually be classified, and generally, after six months, the applicant can proceed with his invention.

 

Z had three such applications, all filed in 1981. The first was abandoned, however the other two were eventually were examined and allowed. The State of Israel never did not do anything with the inventions, and only some 12 years later, lifted the restrictions. Z himself did work to bring a product to market, even after the restrictions were lifted.

 

There is a committee that very occasionally convenes to rule on appropriate compensation. The committee, in its current constellation, rather different from that that first deliberated on this issue, has now issued a ruling and this article reports on the deliberations and ruling of the compensation committee regarding this claim.

 

Since there was no utilization by them, there is no patent royalty payable by the State. Z claimed 22 million dollars compensation for damage caused by the restriction order; the sum being an estimate of anticipated profits had the invention been commercialized.

 

According to the decision, after their allowance, the State of Israel requested re-examination of the patents. However, the patent office refused, pointing out that the Ministry of Defense could have conducted secret opposition proceedings, and presented a basis for their claim of invalidity.

 

The patents are therefore valid, but Z apparently did not produce adequate justification for the compensation claimed.

The committee offered to pay for an expert acceptable to Z to do a valuation, but Z didn’t take up this offer. However, when given another opportunity to base his claim for compensation, he provided details of direct expenses laid out, based mostly on 1700 hours work at his consultancy rate of $250 and requested compensation, regardless of culpability of the State. 

 

Z could only produced one receipt showing that in 2005 he could bill at $250 an hour for consulting. The State claimed that the expenses were inflated and not substantiated.  Z claimed that the very fact that a restriction order issued, was grounds for statutory compensation.

 

The case hinged on whether real damage had been done. Could the plaintiff prove his case? Should the fact that the State effectively prevented him from attempting to monetize his invention be taken into consideration when any damage was purely speculative, since there were no sales?

 

The committee appeared to be very uncomfortable with the case before them, but noted that Z was represented by a prominent and very experienced IP litigator and that the Israel system is adversarial and not inquisitional, so they could only rule on the basis of the claims made evidence submitted by the parties.

 

The committee ruled that the law could not be understood as indicative that any application that becomes ‘classified’ automatically deserves compensation as that would be an incentive for filing spurious military inventions. After rejecting that compensation was forthcoming under property rights, unjust enrichment and the like, the committee nevertheless decided that some sort of compensation was in order, and ruled that the wording of the law gave them the rights to rule on compensation based simply on the rule. They assumed that the 200 hours taken to develop the 3rd invention, after the second was conceived, was a reasonable assumption to decide that of the 1700 hours, 1300 were spent on the first, non-compensationable invention, and 200 on developing each of the 2nd and 3rd inventions – bearing in mind the time between the first and subsequent filings, this is not unreasonable.

 

Noting that consultancy fees of $250 or NIS 1000 an hour, obtainable 20 years later after much experience was not a fair basis for calculating how much Z’s time was worth at the time of filing, the committee dismissed this hourly rate as being fanciful.

 

For lack of any better tool, the committee used the most generous Central Govt. Statistics hourly rate of an employed researcher with a Ph.D. in a comparable field in 1981 - the time of the invention. The figure decided upon, and stressed as being the most generous figure they could find in any comparable job description was 6.7 NIS. The committee index-linked this sum, added interest and came up with the almost arbitrary figure of NIS 67,000 which is close to $20,000, or about 1000th of that claimed. 

In the circumstances, they ruled that awarding costs was inappropriate. 

 

Comment

 

Public security should certainly override personal enrichment, and the restriction order, which has its parallels in other patent systems, is therefore reasonable. However, presumably there was some value to the technology or the restriction order would not have issued.

 

The main problem with critiquing the decision is that there are too many unknowns. Was the invention valuable or worthless? Did the Ministry of Defense simply lose the file, or had they tried to implement the invention and only on failing to do so, decided it was worthless. There are, of course, a large numbers of patent applications that are filed that have dubious scientific basis. Many more are not commercially practicable.

 

That said, I am not convinced by the court’s assertion that pending patents cannot be considered property and that they only become property on issuance, and therefore preventing a patent for issuing does not mean that there is no tort under property laws. There are well established speculative markets for options, futures, bonds and the like. I do not think that a patent issuing creates property. Rather it assigns property created by invention to the inventor/applicant for a period of up to 20 years.

 

Whereas many patent applications do not result in commercial goods, there are inventions that have real commercial value and where the inventor is prevented from commercialization by the State, it is difficult for a committee to determine the worth of the invention.

 

Counsel for Z is an eminent IP litigator but is not a scientist. Neither are the committee members. Valuable inventions often appear to be light years away from commercialization at the time of conception, but some are eventually commercialized.

The invention may have required significant development and perhaps was not enabled. The application may, therefore, have been invalid on the grounds of lack of enablement. It’s difficult to tell without running experiments or examining the case. I don’t think the examiner or the committee could tell either.  In cases like this I am not sure whether the attorneys argue the law theoretically, or whether they have full access to the application as filed. I am not sure that it would necessary make a difference.

 

Did the Ministry of Defense attempt to develop the invention and subsequently determine that the concept was fundamentally flawed? Was the application overlooked for 10 years due to applicant negligence, compounded by his attorney, as may be inferred from the decision, or was there nowhere for the applicant to turn? Maybe, he worked on other inventions and this was side-tracked, but was, nevertheless, potentially valuable, and were the military to have encouraged him, could have had real value? The Ministry of Defense argues that even with the patent application restricted, the inventor could have manufactured and requested an export license. I think this may be true, but is irrelevant since without a patent portfolio, manufacturing would have rendered development and marketing pointless. 

 

A famous and significant case regarding restricted inventions was an invention by the actress Hedy Lamarr, the actress who starred in Ecstasy and went on to play Delilah in the Cecil B. de Mille epic.

 

Whilst married to Mandl, a prominent German arms dealer and Nazi sympathizer, and the first of six husbands, she overheard discussions on the problems of torpedo navigation and together with magician George Antheil who provided enablement based on the drum of a mechanical piano, filed a patent application for frequency hopping in 1941, that issued a year later as US 2,292,387, but was restricted for decades. It is now widely used in mobile telephony.

 

Incidentally, instead of using her inventive talent, the US Government decided that her contribution to the War Effort would be selling kisses for War Bonds.


Follow

Get every new post delivered to your Inbox.

Join 103 other followers