A niche blog dedicated to the issues that arise when supplementary protection certificates (SPCs) extend patents beyond their normal life -- and to the respective positions of patent owners, investors, competitors and consumers. The blog also addresses wider issues that may be of interest or use to those involved in the extension of patent rights. You can email The SPC Blog here

Monday, 19 May 2014

More references, more gaps?

... unless it has been
caused by the CJEU
"Two gaps instead of one: the CJEU's effect on Supplementary Protection Certificate jurisprudence" is the title of the June 2014 Guest Editorial in the Journal of Intellectual Property Law & Practice (JIPLP), written by editorial board member and patent attorney Darren Smyth (EIP, London). In keeping with normal JIPLP practice, the full text of this editorial is posted on the journal's informal jiplp weblog, here.

Darren concludes:
"You have all the guidance from the CJEU you are going to get. Every referral you make will result in more “gaps”, not fewer, in the legislative framework. Decide some cases; aim for consistency; but if there happen to be some anomalies, well, it is better than spending the time, effort, and money on a referral that will simply make the issues more complex than they were to begin with".

Friday, 16 May 2014

New home for SPCs on UK government portal

The UK Government's GOV.UK portal now has an SPC page, "Apply or extend a supplementary protection certificate", which you can check out here.  This page houses the 32-page guide for applicants which was last revised in November 2013.

The UK Intellectual Property Office still has its own website, but this too will soon be drawn into GOV.UK.

Thursday, 8 May 2014

Swiss paediatric extensions: a swift answer from the "crowd"

Following this morning's blogpost calling for a crowd-sourced response to a plea for information as to where Switzerland currently stands with regard to paediatric extensions, we have received the following response from a two-man crowd consisting of Simon Holzer & Kilian Schärli (meyerlustenberger | lachenal Rechtsanwälte) who write:
Crowds of Swiss Rechtsanwälte gather round to answer
readers' questions -- but Simon and Kilian were first!
On 7 May 2014, the Swiss National Council adopted the revision of the Swiss Therapeutic Products Act (see excerpt of the Official Bulletin of the National Council of 7 May 2014 [in German and French only]). The legislative proposal now goes to the Council of States. The Federal Office of Public Health, which is leading the revision of the Therapeutic Products Act, expects that the revised version will come into force on 1 January 2016. 
With regard to transitional provisions the new Art. 140o of the Swiss Patent Act stipulates that the application for the paediatric extension can be filed no earlier as with the application for the grant of an SPC and no later then two years before the expiry of the SPC, but no later than six months after the first authorization to place the product on the market as a medicinal product in the European Economic Area with the exception of the Principality of Liechtenstein, and only if the associated medicinal product information reflects the results of all studies that have been carried out in compliance with the paediatric investigation plan considered during the marketing authorization. Further, the new Art. 140s para. 2 sets forth that for the procedure (as well as for the register and for the publications) the rules of the European Union shall be taken into account. 
More information can be found on the following websites:
  • Federal Office of Public Health, here
  • Swiss Agency for Therapeutic Products, here
  • Swiss Federal Institute of Intellectual Property, here
Thanks so much, Simon and Kilian -- this is really helpful!

Swiss paedriatric extensions: where are we now?

One of our readers has asked if he might use the good services of this weblog in order to crowd-source the following question:
What is the legislative status of the Swiss law that is intended to introduce paediatric extensions, similar to the existing EU law?
He tells us that the most recent information he has been able to find on the internet about it is from July 2013. So, he wonders, when is the law going to be introduced, and are any transitional provisions intended?

If you have any current information and don't mind sharing it, we'd be delighted to know -- and so would our reader.

Wednesday, 7 May 2014

The trio of Article 3 CJEU decisions from December 2013: a new article

News comes from our good friend and occasional contributor Mike Snodin (Avidity IP) that an article of his has recently been published in the Journal of Intellectual Property Law & Practice (JIPLP).  The article reviews, analyses and comments upon the decisions in Cases C-443/12 (Actavis v Sanofi), C-484/12 (Georgetown University) and C-493/12 (Eli Lilly v HGS). While noting areas that have been clarified and speculating upon strategies that may now represent "best practice" in the light of the decisions, the article also points out the many areas of uncertainty that still remain -- or that have been generated by the decisions.

This useful six-pager can be accessed by clicking this link.

JIPLP has proved to be a rich source of articles and current intelligence notes on SPCs since it was launched at the end of 2005. Could it be anything to do with the fact that this blogger is its editor?  At any rate, you can get an idea of the range items addressing SPCs by clicking here.  Mike has previously published in JIPLP, as have many other readers of or contributors to this weblog.

Friday, 25 April 2014

Fordham Report 2014: SPCs

"They have confused more than they have clarified", declared moderator Gonzalo Ulloa (Gómez-Acebo & Pombo, Madrid), amid general rumblings of assent from the audience, when referring to the recent decisions of the Court of Justice of the European Union (CJEU) on Supplementary Protection Certificates. The occasion was a dedicated session at this year's Fordham IP Conference (programme here).

Brian Cordery (Bristows, London) spoke first: SPCs continue to be a hot topic in Europe, he explained. 2013 witnessed several further referrals to the CJEU and several more rulings have emerged. While it is possible to pick out a line of logic in the decisions, his theme was that much uncertainty remains and that the recent rulings have arguably confused as much as they have clarified. Brian offered a rapid, condensed review of the recent case-law, focusing closely on Eli Lilly v HGS (Tabalumab), a case that is coming back to Mr Justice Warren next week.

Rian Kalden (Court of Appeal of The Hague, The Hague) spoke next, addressing Actavis v Sanofi and whether you can obtain more than one SPC per patent. Georgetown indicated that it was possible to get two SPCs where the basic patent protected both combination products as well as the underlying product, making three in all.  Jürgen Dressel (Novartis Pharma AG, Basel) then offered an update on second medical use. He explained that legislators and courts in all developed countries have recognized both the value and the patentability of innovation stemming from clinical research. Jürgen's conclusion was that only now -- and very slowly -- have patent offices and courts began to learn how to deal with clinical inventions in a way that is fair to all stakeholders. Further stimulation of such important innovation business certainty and therefore a globally harmonized approach to patentability requirements and enforcement are thus of utmost importance.

In his presentation Jürgen led the audience through the process of research, development, through to market authorisation and commercialisation, observing that different types of claim, recognised in different jurisdictions, led to the protection of different concepts -- including second medical use.  He acknowledged that this was a matter of interest both to drug originators and to manufacturers of generic products and mentioned that this was a topic for the forthcoming AIPPI conference in Toronto. He also strongly recommended that conference participants read the well-reasoned judgment of Birss J in Hospira v Genentech (blogged for the IPKat by Darren Smyth here).

The panellists at this session were Laëtitia Bénard (Allen & Overy LLP, Paris), Joachim Feldges (Allen & Overy LLP, Munich) and Christine Kanz (Reimann Osterrieth Köhler Haft, Düsseldorf). Joachim raised the question of whether the function of the CJEU was to interpret EU law or to clarify it. He also added to the speculation regarding the treatment of patents with Markush formulae. Are some features of a claim "second class" because they only deal with the form and not the substance of a structure, he asked, and should any distinction be made once a patent has been granted? Sadly, we have to refer questions to the CJEU, he concluded, and the questions are a good deal clearer than the answers.

Christine observed that the CJEU was composed of legal generalists who struggled to appreciate what the SPC Regulation was about. The court appeared to be adopting an "inventive advance" approach without actually saying so, thereby importing patent law concepts into SPC law.

Inevitably, discussion took place on the meaning and significance of the term "necessarily and specifically" in the ruling of the CJEU in Eli Lilly v HGS that
Article 3(a) ... does not, in principle, preclude the grant of a supplementary protection certificate for that active ingredient, on condition that it is possible to reach the conclusion on the basis of those claims, interpreted inter alia in the light of the description of the invention, as required by Article 69 of the Convention on the Grant of European Patents and the Protocol on the interpretation of that provision, that the claims relate, implicitly but necessarily and specifically, to the active ingredient in question, which is a matter to be determined by the referring court".
This blogger was comforted by the fact that others seem to find it as difficult to appreciate the subtlety of this phraseology as he does.  He was however heartened by an intervention from the floor by respected academic Martin Adelman (George Washington Law School, Washington DC) to the effect that there was no threat of "evergreening" of a patented product since there is no jurisdiction in the world that provides for the possibility of evergreening a patent. "Anyone who uses the term 'evergreening'", remarked the professor, "is engaging in propaganda".

Mr Justice Arnold, speaking from the floor, observed that the CJEU has tended to formulate its rulings on SPCs in relation to the facts relating to the patent concerned in the reference before it, and not to the underlying legal issues [or to the terms of the marketing authorisation ...]. Further confusion has been caused by the CJEU's tendency to discuss policy issues without relating them explicitly to earlier case law which references from national courts invite them to reverse.

The full text of this session, once corrected, will be published in its entirety by Fordham University. It was simply not possible to provide an accurate summary of the speakers' presentations in real time, so The SPC Blog will let you know when the full, revised text has been made available.

Sunday, 20 April 2014

Portugal adjusts term to match CJEU order

From our friend João Jorge (RCF - Intellectual Property, Lisbon) comes the following information for which we gratefully thank him:
As a consequence of CJEU Decision C-555/13 (that's Merck Canada, noted on The SPC Blog here), the Portuguese PTMO has released on 17 April a Directive from the Board (2/2014), dated 10 April, informing that a verification is to be conducted to ensure that the term for all SPCs complies with the referred decision ensuring that "the 15 years exclusivity defined in that CJEU decision is not exceeded".

In practice this decision will affect about 30 SPCs currently in force, all corresponding to products in the market as SPCs normally do.

This Directive was not unexpected.

However, as PT patent attorneys we are used to seeing in this type of change, the PTMO has already corrected the term in the online database and has sent notifications informing the respective patent attorneys. The effect of the recalculation is that some of the SPCs will have a sudden death, some of them with a new end of validity date that is before the date of entry into force. The others will see a reduction in the duration but still remaining in force.

The Directive has a final note stating that a one month term shall be given to the owners of these affected SPCs that wish to file paediatric extensions but that, due to this recalculation, they would no longer be able to do it. We have to bear in mind that the duration of some of these SPCs was cut by more than two years.

Finally, publication in the Official Journal will be carried out for those SPCs that, with these changes, have already reached the end of their validity. For all the other affected SPCs, no publication is expected to occur.

Just a final note: this publication of end of validity will only happen in 21 April. So, until then what a wonderful grey area for lawyers!"
The SPC Blog also thanks its friends at the Lisbon practice of Baptista, Monteverde & Associados for sending us the link to the same information on the BMA Newsflash, here.

With all this news coming from Portugal, it almost feels as though that lovely country lies right at the heart of Europe and not at its distant Atlantic edge.

Wednesday, 2 April 2014

SPCs and medical devices: disappointment for Cerus

Via this post by Darren Smyth (EIP) on the IPKat weblog comes news of two SPC applications in the name of Cerus Corporation: SPC/GB/07/043 and SPC/GB/07/044.  The outcome of both applications was that authorisation to place a product on the market as a medical device under Directive 93/42 cannot be considered equivalent to authorisation under the medicinal products Directive, Directive 2001/83.  Accordingly, the two applications were held not to comply with Article 3(b) of the SPC Regulation, which requires "a valid authorisation to place the product on the market as a medicinal product has been granted in accordance with Directive 2001/83/EC or Directive 2001/82/EC, as appropriate".  Darren observes that this appears to be the majority view around Europe, though there are some conflicting cases in the Netherlands and Germany where the assessment processes were held to be equivalent and SPCs were allowed.  

The Cerus Corporation decision, dated 31 March, is summarised on the UK IPO website as follows:

EC Design Examination Certificate No. G7 02 05 16178 063 was filed in support of SPC application SPC/GB/07/043 for “Platelet preparation obtainable by addition, and subsequent photoactivation, of amotosalen or its salt, to a suspension of platelets in plasma”. EC Design Examination Certificate No. G7 06 09 60562 004 was filed in support of SPC application SPC/GB/07/044 for “Platelet preparation obtainable by addition to plasma, and photoactivation, of amotosalen or its salt”. These EC Design Examination Certificates relate to medical devices that meet the criteria of Article 1(4) of Directive 93/42/EEC because they relate to a device that incorporates, as an integral part, a substance which, if used separately, may be considered to be a medicinal product and which acts upon the body with action ancillary to that of the device. As a consequence, they fall within class III medical devices and the safety, quality and usefulness of the substance must be verified, taking account of the intended purpose of the device, by analogy with the appropriate methods specified in the medicinal products legislation (Directive 2001/83/EC). Class III devices have the highest risk potential in terms of the vulnerability of the human body (taking account of the potential risks associated with the technical design and manufacture of the device). Explicit prior authorization with regard to conformity is required for such devices to be placed on the market. As a consequence of the need to assess the substance as part of the assessment of the device overall, the applicant argued that these EC Design Examination Certificates can, as a consequence, be considered to meet the requirements of Art 3(b) of the SPC regulation, i.e. they represent a valid authorization to place, on the market as a medicinal product, the product for which an SPC has been applied for.
The hearing officer reviewed the SPC regulation and the relevant parts of the medical devices and medicinal products directives. He took account of the purpose of both codes, the means by which medicinal products and medical devices deliver their principle mode of action, and the actual performance that is being assessed under both codes. He concluded that the assessment carried out in relation to the substance, i.e. the safety, quality and usefulness of the substance, when considered in light of the means by which the medical device delivers its action and considering the process by which a device is approved, including the roles of notified bodies and competent bodies, means that the conformity assessment procedure for a class III medical device is not the same as or equivalent to the process carried out to authorise a medicinal product for human use.
As a consequence, the SPC applications were found not to meet the requirements of Article 3(b) and were rejected under Article 10(2) of the SPC Regulation. 
As ever, readers' comments are invited and appreciated.

Three SPC seminars coming up -- with discounts for SPC Blog readers

From our old friend Rechtsassessor Jean-Claude Alexandre Ho (IP conference manager at FORUM Institut für Management GmbH) comes news of three SPC-related seminars which he is organising. They are as follows:
1. 'Eli Lilly, Actavis, Georgetown II: Quo vadis, SPC?', the update seminar in which Dr Christopher Brückner, the author of the SPC commentary noted here (participants will receive the new second edition on top of course documentation), will speak on the CJEU's "Super Thursday" and on how to understand the decisions and which practical consequences we may expect for the future. Date: 17 June 2014; venue: Amsterdam. More information is available here. SPC Blog readers are entitled to a 10% discount against the registration fee (€ 880 down from € 980). 2. 'Supplementary Protection Certificates', the fifth edition of FORUM's advanced SPC seminar in English. This is a one and a half day course conducted by Dr Brückner (participants will also receive the new second edition of the SPC commentary on top of course documentation). Date: 25 and 26 September 2014; venue: Amsterdam. More information is available here. SPC Blog readers are entitled to a 10% discount against the registration fee (€ 1,200 instead of € 1,340). 
3. 'SPC for Beginners', the third edition of FORUM'S basic SPC seminar in English, once again with Dr Christopher Brückner and his updated SPC commentary as an add-on. Date: 24 September 2014; Venue: Amsterdam. More information is available here. SPC Blog readers are entitled to a 10% discount against the registration fee (€ 880 down from € 980).
To register and gain the benefit of your reduced fee, just forward this blogpost to Jean-Claude himself at jc.alexandreho@forum-institut.de, or call him, quoting "The SPC Blog" (+49 6211 500-675) and specifying which event(s) you would like to attend.

Tuesday, 25 March 2014

U-turn on the U-turn: more comments on the Italian latanoprost antitrust decision

Recently the new decision issued by the Italian antitrust authorities in the matter of the latanoprost case was discussed on this weblog (see earlier posts here and here).

Micaela Modiano (Modiano & Partners) and Anna Maria Stein (Franzosi Dal Negro Setti) now add more information about this important decision, so as to shed some light on why, after the the Italian antitrust authority (Autorità Garante della Concorrenza e del Mercato) had first found that Pfizer had abused its dominant position, and after a first U-turn of the Italian administrative court (Tribunale Amministrativo Regionale) denying that there had been any abuse by Pfizer, the administrative appeal court (Consiglio di Stato) has now taken a further U-turn and instead held that Pfizer has abused its position.

As those of you who have followed this case already know, Pfizer owned a patent with compound claims to, inter alia, latanoprost on which it had filed SPCs and paediatric extensions in various EU countries, but not in Italy. Pfizer had obtained a divisional on the basis of that patent, had validated the patent in Italy, Portugal and Spain and then obtained an SPC and a paediatric extension in Italy on the basis of the divisional patent. At the end of opposition proceedings, the divisional patent had been maintained with claims to the use of latanoprost for a certain therapeutic indication.

The Italian antitrust authority had held that Pfizer had abused its dominant position. Important factors which had led to such decision were the fact that Pfizer had not clearly informed the Italian Patent and Trade Mark Office that the Italian SPC application was based on the divisional while in other EU countries it was based on the parent patent. This was a clear attempt to draw principles from the AstraZeneca case, where AstraZeneca had been found to have intentionally supplied false information to various Patent Offices in an attempt to obtain IP rights and/or or IP right expiry dates to which it was not entitled. It is worth noting that nothing in the SPC Regulation precludes a company from filing an SPC for a product in one country on the basis of one patent and in another country on the basis of another patent, be it a divisional or a wholly different patent. It is also worth noting that Pfizer never made representations to the Italian Patent and Trade Mark Office about the “nature” of its patent, so that the accuracy of the parallel with AstraZeneca appears to be very limited.

The Italian administrative court had in fact denied that there had been any abuse by Pfizer, noting inter alia that Pfizer's behaviour did not include the “quid pluris” (such as an intentional misrepresentation to the Italian Patent and Trade Mark Office) which is necessary for a finding of abuse.

Contrary to this, the Italian administrative appeal court (Consiglio di Stato) has now held that Pfizer did abuse its dominant position. A few of the points made by the Consiglio di Stato to support this position are quite interesting and will probably spur some debate among the lovers (or haters?) of divisionals.

As a first point, even though during the proceedings relating to this antitrust challenge Pfizer had clearly shown that – as is also inevitably based on the provisions of the SPC Regulation - basing the Italian SPC and paediatric extension on the divisional did not lead to an SPC expiry date different from the one achieved by the other SPCs and paediatric extensions which were based on the parent patent, the Consiglio di Stato does not seem to have appreciated this point, since in the decision the court has emphasized that the divisional patent expired in 2009 whereas thanks to the Italian SPC and paediatric extension the expiry date was postponed to 2012 (evidently not realizing that the comparison had to be made among the various SPCs, or the various paediatric extensions, and not between the patent and the SPC/paediatric extension).

Even more notably, on the point of the actual abuse the Consiglio di Stato held that (our English translation):
“Here, we do not discuss a conduct prohibited by patent law, but the anti competitive implications of a number of acts which, in and of themselves, are legitimate [i.e. obtaining a divisional patent and an SPC]. After all, the abuse of a dominant position, attributed to Pfizer, is nothing but the specification of the broader category of abuse of right, whose precondition is in fact the existence of a right, which then is used in an instrumental manner that is not coherent with the goal for which the law acknowledges it – in this specific case, the exclusion of the competitors from the market.”
At this stage, the question that first springs to mind is what other, legitimate, purpose obtaining a patent and an SPC can serve, for the party that obtains such IP rights, if not that of excluding competitors from the market (after all, patents and SPCs, like all IP rights, are exclusive rights). This answer, at least in the view of the Consiglio di Stato, can probably be found in the following passage of the decision (our English translation):
“In the present case, the behaviour adopted by Pfizer by way of the exploitation of the rights connected with the ownership of the main patent and with the position on the market allowed to defer [the entry into the market] of generics of Xalatan, without entailing any concrete use of the same active pharmaceutical ingredient different from the one already protected. The assessment of the [Italian antitrust] authority, who saw in such behaviour a goal going beyond, and differing from, the one that is specific to the patent protection … is therefore fully justified.”
It will not come as a surprise, after reading this passage, that in at least three other passages of the decision the Consiglio di Stato insists on the fact that the grant of the divisional patent was not followed by the marketing of any new product (Pfizer's Xalatan, comprising latanoprost as the active pharmaceutical ingredient, was already on the market when the divisional patent was granted).

Thus what transpires from the decision is that the Consiglio di Stato considered that, for the divisional patent to be legitimate, it had to be accompanied by the marketing of a new product (falling within the scope of the patent). This is in contrast with the fact that, as said above and by definition, patents are exclusive rights and not a permission, let alone an obligation, for the patent owner to implement the invention in actuality. In addition, this is in contrast with the fact that one and the same product can be validly covered by several patents (Markush formula for the active ingredient, salts, polymorphs, process for making the active ingredient, formulation, process for making the formulation, use for a certain therapeutic indication, etc.), none of which require the marketing of a new product for such patents to be valid and non-abusive.

As far as we know, this decision is one of the few decisions on the interaction between divisional patents and antitrust laws in Europe. In addition, the action was started before the Italian authorities as Pfizer's allegedly abusive behaviour was limited to Italy (given that in most other European countries the SPCs and paediatric extensions were based on the parent patent), but throughout the proceedings the parties relied on the case law of the CJEU in the matter of abuse of dominant position and ruled on the basis of Art. 102 TFEU rather than on the exclusive basis of Italian law. It is thus hoped that, if this decision is cited in the future by other authorities ruling on the same issues, this will be done with a view to clarifying whether the exclusive nature of a patent is, in and of itself, a legitimate reason to own a patent or whether each (divisional) patent must be accompanied by a new product for it to be legitimate also from the point of view of competition law.