Martin a. Voet

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proceedings. No translations would be required. Following ratification by at least 13 member states including France, Germany and the UK, the unitary patent system was expected to come into force in 2017. To date it has been ratified by eight countries including France, with Germany and the UK indicating their ratifications will soon follow, though that might now be in doubt in view of the UK’s probable exit from the EU.

      Currently one has to sue infringers in each EU country under each national patent with the potential for different results in different countries under differing national laws, not to mention the time, expense and uncertainty of multiple litigations. When implemented, this new system should greatly simplify obtaining, enforcing and defending patent rights in Europe.

      A patent consists of a multi-page printed document which gives the basic information about itself on the cover page followed by the specification and ending with the claims. The cover page also provides a summary of the invention, but it is written when the patent is filed and it is rarely changed. Since it is a summary of the application when filed rather than a summary of the patent when granted, it is rarely an accurate summary of the granted patent.

      The specification or body of the patent describes the invention and how it is to be used. It typically starts with a description of the field of the invention and describes what was known in the field before the invention was made, the so-called “prior art”. It then describes the invention generally and then again in detail and offers examples of how it works. If it is a patent on a new chemical entity (NCE), it will describe exactly how to make it and what the chemical and physical characteristics of the new compounds are. If it is about a new medical use, it will describe dosage forms, suitable formulations and concentrations of drug to be used and the disease or condition to be treated.

      At the end of the patent document are numbered paragraphs known as “claims”. Claims are the heart and soul of a patent and define the rights granted to the patent holder as a deed to a piece of real property defines the property lines of the property. Litigation concerning a patent always focuses on the claims and each and every word in them. Skilled patent litigators often refer to infringers as trespassers on the property of the patent owner. So to understand a patent, you must first understand the claims.

      The claims of a patent define the scope of the invention. Much time and attention is given to claims and that is what 95% of patent prosecution is about. When you submit the patent application, an Examiner reads it and must make a decision on whether to allow the claims you have presented to become part of a granted patent. Claims tend to be long-winded because the regulations require each claim to consist of a single sentence.

      The broadest patents have the shortest claims. That is because the more you say about something, the more specific you become, which narrows the claim. The broadest claim is one that requires the least said about it. With claims, as with certain other matters in the field of human endeavour, the less said the better.

      For example the shortest and therefore broadest claim I am aware of is in U.S. Patent No. 3,156,523 for an element, Americium, discovered by Glenn T. Seaborg and colleagues at the University of California at Berkeley (a little plug here for my alma mater). Claim 1 reads “Element 95”. You might think an element could not be patented, but recall the transuranium elements are not naturally occurring, so element 95 is man-made and thus patentable. Now that is a broad claim. Seaborg also discovered elements 94–102 and 106 including plutonium (94) and was awarded the Nobel Prize for Chemistry in 1951. His name will live on forever as he also got possibly the longest lasting award one can think of: element 106 was officially named Seaborgium in 1994.

      The goal of a typical patent attorney is to cover the invention with as broad a claim as possible, usually claim 1. After claim 1, a number of more detailed claims typically follow, i.e., narrower claims until the last claim that is generally the narrowest. There is no law requiring this order, so occasionally a broader claim may come later in the series.

      For pharmaceutical patents covering commercial drug products, it is a good idea to have some narrow claims in your patent which cover the commercial drug formulation more or less exactly. While such narrow claims would be relatively easy to design around, it can be the best way to protect a commercial drug against a generic copier who simply copies the commercial formula.

      5. First page of U.S. Patent No. 3,156,523

      6. Last page with claims of U.S. Patent No. 3,156,523

      There are generally two types of claims. One is called independent and the other is called dependent. The independent claim stands on its own, while the dependent one refers to another claim. The dependent claim is a shorthand way of claiming a new feature of the invention without reciting all the old features again. For example claim 1 below is an independent claim followed by claim 2, a dependent claim:

      1 A method for treating spasticity comprising administering to a spastic patient an effective amount of a botulinum toxin.

      2 The method of claim 1 wherein the botulinum toxin is botulinum toxin type A.

      There are other forms of claims with names and much more could be said about them, but the take home on claims is that claims define the scope of the invention and that is what a patent covers, no more and no less. When someone asks what does the patent cover, you must read the claims to find out.

      Abstract ideas, physical phenomena and laws of nature are not patentable, as well as mathematical expressions and purely mental steps such as algorithms and computer programs, except when patented in combination with hardware. Recently, the courts have allowed so-called “business method” patents, such as the one-click ordering of merchandise on the internet, which previously were denied as being purely mental steps. Cloning methods are patentable, but not cloned human beings, though genetically engineered bacteria and mice, among other living things, have been patented.

      The famous Harvard “onco-mouse”, altered to develop cancer, was the first patented transgenic mammal, patented in the U.S. in 1988 under U.S. Patent No. 4,736,866, but it still bothers some people that “life” can be patented. In 2004, the European Patent Office finally upheld the corresponding European patent, which initially had been approved in 1992, against objections by church, environmental and animal protection groups, including Greenpeace, who had argued for cancellation on the grounds that it violated the dignity of living beings.

      The U.S. Supreme Court weighed in on the issue of what is patentable in 2010 in the case of Bilski v. Kappos by ruling a method of hedging risk in the energy market was not patentable as an attempt to patent an abstract idea.

      In 2012, the Supreme Court also unanimously decided the important Mayo v. Prometheus pharmaceutical case. The Prometheus invention related to a method of optimizing therapeutic efficacy for treatment of a medical disorder by identifying relationships between concentrations of certain metabolites in the blood and the likelihood that a dosage of a certain drug (thiopurine) would prove either ineffective or cause harm. Claim 1 for example stated that if blood levels of a certain metabolite exceeded a certain level after a specified dose of that drug, then such dose would produce toxic side effects.

      The Court found that the claimed relationship was a consequence of the way in which thiopurine compounds are metabolized by the body, which is an entirely natural process. And so a patent that simply describes that relation sets forth a natural law and is therefore not patentable. The conclusion here is that a newly discovered law of nature is not patentable and the application of that newly discovered law is also not patentable if the application merely relies upon known elements.

      What about newly discovered naturally