Can Unjust Enrichment Be Used To Justify An Injunction Against Competitors During The Patent Opposition Period?

June 6, 2011

In an important ruling, the Israel Supreme Court has upheld a refusal of the Tel Aviv District Court to grant an injunction to Merck, the applicant for a pharmaceutical patent for Focalin, to prevent generic competitors from exploiting a patent during the post examination opposition period. The grounds for the injunction attempt were Unjust Enrichment. Since the1981 A.Sh.I.R. appeal where the Supreme Court upheld three decisions to grant injunctions for designs that were never registered under the Law of Unjust Enrichment, there has been a cloud of uncertainly as to whether unjust enrichment could be used as the basis for injunctions where there are no patent rights. This decision addresses this issue. 

Background

InIsrael, a patent application only publishes once it has been found patentable by the Examiners. On publication, an opposition may be filed, and if this does not happen, a patent issues three months later. If an opposition is filed, a patent will only issue if and when the opposition is rejected.

Because of the large stakes, pharmaceutical patents are very likely to be opposed. The drug developers accuse generic industry opponents to their patents as opposing everything in bad faith. The generic companies accuse drug developers of ever-greening and of filing patent applications that lack novelty and inventiveness over earlier patents. There is some merit in the positions of both sides.

The Case

Merck have tried to obtain an injunction against generic manufacturers Teva, Unipharm, Trima and Zevulun Tomer (owner of Unipharm) to prevent them manufacturing generic equivalents of Focalin 70 mg during the patent opposition. Focalin is a drug used in the treatment of osteoporosis.

The argument used by the patent applicant to request the injunction was that although the Patent Law provides for retroactive compensation for exploitation by others during the opposition period, should a patent eventually issue, the damage is irreversible and no adequate compensation is possible. Following A.Sh.I.R. ruling by the Israel Supreme Court in 1981, IP laws and Unjust Enrichment can coexist.

The generic manufacturers argued that the Israel Patent Law provides a correct balance between the interests of both sides and that of the public, and there is no logic to the courts altering the balance in the Law that the legislative have decided upon. Additionally, until a patent issues, there is no patent, i.e. no asset, so unjust enrichment by misappropriating the asset cannot happen. They also pointed out that the public interest is in competitive markets and cheap drugs. Monopolies exist only where the legislation grants them, and it was against public policy for the court to extend monopolies where the law does not provide them.

The Court of First Instance rejected Merck’s application for Unjust Enrichment, and Merck appealed to the Supreme Court claiming that the issue had been ruled on narrowly based on legal grounds without sufficient regard to the business context which was characterized by inequitable behaviour.

The Supreme Court requested that a spokesman for the government explain the govt. position. The Supreme Court went on to rule that the Patent Law offers a balance between the various interests that reflects the desires of the legislature and does not require adjustment. Furthermore, the Law of Unjust Enrichment only applies where there is no legislative solution. The Appeal was rejected.

Costs of NIS40,000 (about $ 12,000 US) were awarded against Merck.

Comment

I think the Supreme Court was correct to reject the appeal, and am happy that there is now a legal precedent in this important area.

The publication of the patent inIsraelis, of course, largely irrelevant in terms of teaching the public, since most jurisdictions publish automatically 18 months from priority. That as may be, to misquote Appeal 20/82 (Adres vs. Harlow and Jones) since the A.ShI.R decision the specter of Unjust Enrichment hung, like a vulture, over the IP playing field. I am pleased that this is no longer the case. An interesting question, not addressed in this instance, is whether the courts can and should order the opposer to file a bond to discourage unfounded oppositions and to provide a kitty should the defendant, which may be a limited company, going out of business if and when a patent issues.

The original ruling related to the fact that the generic manufacturers rely on regulatory approval based on evidence provided by the patent developer and that this was also Unjust Enrichment. This aspect was not appealed.


Canada Supreme Court to Hear Challenge to Pfizer’s Viagra Patent by Teva Canada

May 9, 2011

The Supreme Court of Canada has announced that it would hear Teva Canada Ltd.’s challenge to Pfizer Inc.’s patent for Viagra. The high court granted Teva Canada’s leave to appeal without comment Thursday, agreeing to review a September 2010 ruling from Canada’s Federal Court of Appeal that barred Teva Canada from producing a generic version of the drug prior to Teva Canada could not produce a generic version of Viagra until Pfizer’s Canadian patent expiring.


Patent for Hydrated Salt of Risedronate Refused in Israel Opposition

May 4, 2011

Risedronate is used for the treatment of Paget’s disease of bone, a disease in which the formation of bone is abnormal, and for treating sufferers of osteoporosis in which the density and strength of bones are reduced. By slowing down the rate at which bone is dissolved, risedronate increases the amount of bone. The FDA approved risedronate for treatment of Paget’s disease in 1998 and for the prevention and treatment of osteoporosis in 1999. The drug is marketed as Actonel.

Proctor & Gamble filed worldwide patents titled for WO/2001/056983 ”Selective Crystallization of 3-Pyridyl-1-Hydroxyethylidene-1,1-Bisphosphonic Acid Sodium as the Hemipentahydrate or Monohydrate.” This patent has issued in Korea, Europe and the US. After allowance in Israel, it published for Opposition purposes and Unipharm filed an opposition. The claims in Israel were those allowed in the US.

The main claim is:

A process for selectively producing 3-pyridyl-1-hydroxyethlidene-1,1-bisphosphonic acid sodium hemipentahydrate and monohydrate comprising the steps of:

a) providing an aqueous solution of 3-pyridyl-1-hydroxyethlidene-1,1-bisphosphonic acid sodium;

 b) heating the aqueous solution to a temperature from about 45° C. to about 75° C.; c) adding a solvent to the aqueous solution; and

 d) optionally cooling the aqueous solution.

The Opposer claimed that the applicant knew full well that the hydrated salt was a mixture of the hemipentahydrate and the monohydrate and that the method of crystallization was the standard method of dissolution and was totally lacking in inventive step. The Applicant claimed not to have been aware of the monohydrate, although it is apparently always precipitated with the hemipentahydrate.

Deputy Commissioner Noach Shalev Shlomovits who heard the opposition, was apparently impressed by the fact that neither in the application nor during the opposition proceedings, did the applicant produce any crystallographical evidence, but simply deduced the two salts from the weight of the crystals, estimating the water of crystallization. Without any other evidence, it is clear that both crystal forms must have been known, and it appears that the general observation of controlling the rate of cooling and concentrations does not involve an inventive step. Shlomovits ruled that not only was there a lack of inventive step, but that the application was not properly enabled. Furthermore, he states that the claimed invention is not fairly based on the specification. Additionally, for greediness in clearly claiming more than is entitled, the Deputy Commissioner ruled that the application should be rejected. Finally, he stated that the scope of the composition claims include the pure hemipentahydrate which the applicant accepted was previously known since it was claimed in an earlier application.

Comments

The decision is resplendent with words like obvious’ and clearly, yet it should be noted that other, significant examining jurisdictions did allow the patent. Nevertheless, claims 16 to 18 relate to mixtures of from 50%-100% hemipentahydrate which does indeed lack novelty due to previous patents for the salt. Is this an attempt at ever-greening? Perhaps. If the applicant is dissatisfied with the Deputy Commissioner’s analysis, this decision will be appealed to the courts.

It should be noted that Teva tried unsuccessfully to invalidate the main Actonel patent in 2008. Earlier this year Teva was sued by Roche and by Warner Chilcott for patent infringement when trying to obtain FDA approval for a generic version of the drug.


Israel returned to the US Special IP Report Blacklist

May 4, 2011

Back in 2010 we reported on an agreement reached between Israel and the US in Washington, where the Israel delegation, headed by the Israel Ministry of Industry, Trade Director General Sharon Kedmi agreed to amend the Israel Patent Law regarding pharmaceutical patent term extensions, in return for which, the US dropped Israel from the blacklist of countries with inadequate IP protection in the Special 301 report, relegating Israel to the watchlist only. See Israel to be Downgraded to US Special 301 Watch List and Proposed Amendment to Israel Patent Law made Public for more details.

Although a draft amendment was circulated to patent attorneys, IP lawyers and others for their comments, the amendment was never passed.

Consequently, Israel has been returned to the blacklist.

COMMENT

This development is not surprising. I don’t think the position adopted by the US is a more moral position or an objectively better balance between free market competition and patentee’s results, nor do I think the amendment is warranted. I see this as simply an example of US protectionist bullying.

Then again, paraphrasing the late great Groucho Marx, who’s interested in joining a club that would have them as a member?


EU Announces Anti-trust Probe into a Cephalon – Teva Deal Concerning Generic Provigil

April 29, 2011


The European Union’s antitrust watchdog said Thursday it had launched an ex officio probe of U.S. pharmaceutical giant Cephalon Inc.’s alleged attempt to pay Teva Pharmaceutical Industries Ltd. to keep Modafinil, a generic version of narcolepsy drug Provigil off the market.

Provigil is a stay-awake drug that is used to treat the sleeping sickness narcolepsy and also became popular among night-workers such as truckers and has been tested for military use. It enables users to stay awake for days. (I couldn’t find any information as to whether it works during lectures).

The probe concerns a deal struck between the Cephalon and Teva that “may have had the object or effect of hindering the entry of generic Modafinil” into the European Economic Area.

The case arises from a December 2005 deal to settle patent infringement disputes in Britain and the United States, which saw Teva undertake not to sell its generic Modafinil products in the European single market before October 2012. The probe does not indicate “a definitive finding of an infringement. There is no set deadline for an outcome. Various side deals are also under investigation by US antitrust authorities.

Generic drugs are far cheaper, typicaly costing about 40 percent less than the first, patented drug. The EU has been probing the sector repeatedly since a report showed that the number of new drugs reaching the market annually had dropped by over a third since 2000 and that people were being deprived of innovative, affordable and safe medicine.

What is clear from this probe is that whilst supplementary protection certificates (SPC) are available in Europe to prolong patent protection for the first patent for a new drug, the European Union sees generic drug availability as in the public interest. The law tries to strike a balance and cartels that upset this delicate balance are unacceptable.


Cosopt Patent Remains Dead – Teva to Produce a Generic Version of the Glaucoma Treatment

April 11, 2011


A U.K. appeals court has rejected an attempt bid by Merck & Co. Inc. to revive a European patent covering Cosopt, paving the way for Teva UK Ltd. to push forth a generic version of the glaucoma treatment.
Merck & Co., is the second-biggest U.S. drug company. Teva UK is a subsidiary of Israel’s Teva Pharmaceutical Industries, the world’s biggest maker of generic drugs.
Teva sued Merck three years ago claims the patent shouldn’t have been granted after Merck filed the application in 1992. The Appeal upheld a November 2009 ruling that Merck’s patent lacked novelty or inventiveness was correct because experts in the field would have found the development to be obvious.
COSOPT (dorzolamide hydrochloride-timolol maleate ophthalmic solution) is the combination of a topical carbonic anhydrase inhibitor and a topical beta-adrenergic receptor blocking agent.
Glaucoma is a disease of the optic nerve which receives light-generated nerve impulses from the retina and transmits these to the brain, where we recognize those electrical signals as vision.
Glaucoma is characterized by a particular pattern of progressive damage to the optic nerve that generally begins with a subtle loss of side vision (peripheral vision). If glaucoma is not diagnosed and treated, it can progress to loss of central vision and blindness.


Cubist and Teva Resolve Dispute

April 7, 2011

Cubist Pharmaceuticals Inc. and Teva Pharmaceutical Industries Ltd. (TEVA) have resolved their dispute by Cubist agreeing to license its antibiotic Cubicin to Teva . Under the agreement Teva can start selling its generic version in June 2018 if Cubist is granted a six-month extension of marketing protection for pediatric use.

The patent is due to expire in September 2019. Without pediatric clearance, Teva may sell Cubicin starting in December 2017.

The case: Cubist Pharmaceuticals Inc. (CBST), v. Teva Parenteral Medicines Inc., 1:09-cv-00189-GMS, U.S. District Court, District of Delaware (Wilmington).


Counting Sheep for Insomnia – Do sheep count???

March 9, 2011

Neurim’s appeal against the refusal of the UK Patent Office to issue a Supplementary Protection Certificate for Circadin has been referred to the European Court of Justice –the CJEU by the Court of Appeal.

Background

Before a new drug is allowed to be used, regulatory approval is required. This typically takes several years and the drug usually reaches the market towards the end of the 20 years of regular patent protection. It will be appreciated that to bring a drug to market costs hundreds of millions of dollars and very few potential drugs obtain regulatory approval and can be prescribed. There is generally believed to be a market failure in the regular patent regime in that the period over which the patent enables the company that developed a drug to sell at monopolistic prices is considered insufficient to enable the drug developer to recoup their investment and make a reasonable profit.

It is therefore argued that under the standard patent term, there is no incentive to develop and bring new drugs to market. Consequently, various countries that have drug development industries, or which are bullied by countries having drug development industries have adopted patent term extensions, or, as they are called in Europe, Supplementary Protection Certificates (SPCs) which effectively extend the patent for up to an additional 5 years beyond the regular patent protection period of 20 years from filing.

There is, however, a catch. To prevent evergreening – extending patents indefinitely thereby preventing generic competition – such Supplementary Protection Certificates (SPCs) may only be obtained following the first regulatory approval.

The case

Neurim, an Israeli ethical drug company has developed a revolutionary and patented treatment for insomnia based on use of the natural hormone melatonin. The drug, called Circadin, took 15 years to obtain regulatory approval from when their first patent application (European Patent Number EP (UK) No. 0 518 468) was filed on 23 April 1992.

On obtaining regulatory marketing approval in June 2007, Neurim requested an SPC under Art. 3(d) of the SPC Regulation EEC 1768/92 (now EC 469/2009), claiming that this was the “first authorization to place the product on the market as a medicinal product”.

However the British Intellectual Property Office (UK IPO) refused the request on the basis that Circadin was not the first marketing authorization for Melatonin, since another party had obtained approval for “Regulin”, a melatonin medicine for sheep, back in 2001, issued by the UK Veterinary Medicines Directorate under Directive 81/851/EEC. The decision was appealed to and upheld by the court of first instance, and was then appealed to the Court of Appeal who has referred the case to the CJEU.

The Court of Appeal was required to interpret Art 3 of the SPC Regulation and determine whether a valid authorisation had been given for “the product” in question.

The UKIPO argued that melatonin was “the product” and therefore authorisation had been given when it was approved for use in sheep. Neurim argued that sheep were irrelevant – an SPC is just that: protection supplementing the protection of the basic patent. Therefore, as each patent can have its own SPC (but only one), the relevant Marketing Approval for that patent is a marketing approval for a product falling within the scope of that patent.

In the Court of first instance, Justice Arnold was of the opinion that the Regulation was clear, and upheld the IPO’s assessment of the relevancy of the sheep. The Court of Appeal was not so convinced:

Lord Justice Jacob:

“We consider that Neurim’s arguments are not only tenable: in our view they are right. Many kinds of valuable pharmaceutical research will not get the encouragement or reward they deserve if they are not. Pharmaceutical research is not confined to looking for new active compounds. New formulations of old active substances are often sought. Most are unpatentable but from time to time a real invention is made and patented.

Moreover there is much endeavour to find new uses for known active ingredients. The European Patent Convention 2000 has indeed made the patenting of inventions in this area clearer. Its effect is that a patent for a known substance or composition for use in a method of treatment is not to be regarded as old (and hence unpatentable) unless use for that method is known. It would be most unfortunate if second medical use patents could not get the benefit of an SPC.”

For more information, see: the SPC Blog here and here

Court of Appeal: Neurim Pharmaceuticals v The Comptroller-General of Patents [2011] EWCA Civ 228.

COMMENT

Neurim’s Circadin is the only ethical drug other than Teva’s Copaxone that has been developed and brought to market by an Israeli company. The patent in question, and the other patents in Neurim’s portfolio was drafted and prosecuted by my late partner, Dr Stanley Davis.

JMB, Factor & Co. weren’t involved in requesting the SPC in the UK, but have been involved in a corresponding request to the Israel Patent Office. Under current Israel Law (pending an amendment), the extension available in Israel is for the shortest extension granted by a country offering patent term extensions. Consequently, the extension in Israel may be invalid due to the UK case.

Strange things happen when prosecuting pharmaceutical patents. In Korea, a scientific paper relating to Melatonin in cod fish was cited against the corresponding application as rendering treatment by melatonin obvious. One would imagine that fish and humans have very different physiologies. By comparison, sheep and humans are somewhat similar, but Regulin is not a treatment for insomnia in sheep (I believe they count people to induce sleep).

Apparently Regulin improves the reproductive performance of pure bred and crossbred lowland sheep which are to be mated early in the season before the usual peak of reproductive activity. Regulin is recommended for use in Suffolk and Suffolk cross type flocks to cause lambing to start between early December and mid January and in Mule and halfbred flocks to start lambing between late December and mid February.

We await developments with interest.


Warner Chilcott and Roche Sue Teva Over Actonel

January 27, 2011

Following attempts by Teva to obtain regulatory approval of a generic form of Actonel (risedronate), used to treat or prevent osteoporosis and to treat Paget’s bone disease, Warner Chilcott Co. LLC and Hoffmann-La Roche Inc. have launched a suit alleging Teva Pharmaceuticals USA Inc. has infringed one of their patents.


Teva in court over Astra’s Seroquel

January 24, 2011

Israel’s Teva Pharmaceutical Industries has launched a High Court action in London to revoke the European patent for Seroquel, an anti-depressant developed by AstraZeneca.

Currently, no further details are available.


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