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

Showing posts with label Australia. Show all posts
Showing posts with label Australia. Show all posts

Friday, 30 November 2012

Australian patent term extension: here's a blog to watch


The SPC Blog has been closely watching developments in Australia, where a serious no-holds-barred review of pharmaceutical patent protection, taking in patent term extension is in full swing.

This blogger received this email this morning:
Recently, the Pharmaceutical Patents Review Panel released a Background and Suggested Issues Paper in regard to patent extension of term provisions. We are aware that your blog has contained posts relating to pharmaceutical patents in the past and thought you may be interested in the issues under review and the views posted on the Pharmaceutical Patents Review blog.

The Pharmaceutical Patents Review blog can be accessed at the below link:

http://pharmapatentsreview.govspace.gov.au/

Kind regards

Pharmaceutical Patents Review Secretariat IP Australia
At present the Pharmaceutical Patents Review blog has just two items posted on it, but it may be a good idea to watch it closely and see what sort of responses are posted -- and from whom.

Thursday, 22 November 2012

Patent term extension: Australia issues Issues Paper

Just over a month ago, in "Australia takes aim at SPCs: will they survive?", here, The SPC Blog announced the no-holds-barred review of pharmaceutical patents which was about to take place in Australia.  IP Australia has now issued the following information:
Pharmaceutical Patents Review Panel releases Issues Paper

The Pharmaceutical Patents Review Panel has released an Issues Paper, inviting the public to make submissions by 21 January 2013.  The Panel conducting the review will submit a final report to Government in April 2013.

The review will evaluate whether the system for pharmaceutical patents is effectively balancing the objectives of securing timely access to competitively priced pharmaceuticals, while fostering innovation and supporting research. In particular, the extension of term provisions will be reviewed.

The public are also invited to contribute to the review by commenting on the review's blog. The Review Panel will be posting topics and papers on the blog for further discussion during the review.

See the Background and Suggested Issues paper
The Background and Special Issues paper is 72 pages long; patent term extension is dealt with on pages 4 to 14.

This blogger is not certain how inclusively the word "public" is understood within the context of the review, but suspects that its intention is to encourage a wide range of responses rather than merely those from the various sectors of the pharma industry.

The SPC Blog thanks Anna Feros (Shepherd and Wedderburn LLP) for the link.

Wednesday, 17 October 2012

Australia takes aim at SPCs: will they survive?

Is Australia going to take the major step of abolishing SPCs?  The prospect is not as startling or remote as it seems, judging by this information from IP Australia (thanks, Anna Feros, for the link). The announcement reads as follows:
"GOVERNMENT LAUNCHES REVIEW OF PHARMACEUTICAL PATENTS

The Australian Government is taking practical steps to ensure that the patent system is delivering effective outcomes for consumers and industry with the appointment of an expert panel to review pharmaceutical patents. The Panel will seek public comment before submitting a final report to Government in April 2013.

The Australian Government is taking practical steps to ensure access to affordable medicines, while fostering innovation and research, with the appointment of an expert panel to review the appropriateness of the extension of term arrangements for pharmaceutical patents.

The review panel announced today by the Parliamentary Secretary for Industry and Innovation, Mark Dreyfus, comprises:
Mr Tony Harris, former NSW Auditor-General and Parliamentary Budget Officer, as Chair; 
Professor Dianne Nicol, Associate Dean, Research, of the University of Tasmania; and 
Dr Nicholas Gruen, CEO of Lateral Economics.
The review will evaluate whether the system for pharmaceutical patents is effectively balancing the objectives of securing timely access to competitively priced pharmaceuticals, while fostering innovation and supporting research. In particular, the extension of term provisions will be reviewed.

Currently under the Patents Act 1990, patents for pharmaceuticals may be extended by up to five years beyond the standard 20 year term. The extension of term provision was introduced in 1998 and is due for review.

The Panel's final report is due to be provided to the Government in early 2013. A public consultation process will form part of the review.

We will provide secretariat and research support to the review.

For more information, contact Sean Applegate on (02) 6283 2207".
Readers' comments are welcome, as usual. A cynic might suggest that, in global terms, Australia can easily scrap SPCs without fear that "fostering innovation and supporting research" will be harmed since the Australian market is a relatively small one and no serious pharma company is going to shut up shop just because it stops giving SPCs, for at least as long as plenty of other countries with lucrative domestic markets continue to offer patent term extension.  Come to think of it, Australia might want to contemplate abolishing its patent system in its entirety for much the same reason ...

Here's some data concerning the Australian pharmaceutical sector.

Wednesday, 17 June 2009

Australian Patent Office allows patent term extension for a drug delivery system for two or more active substances

The Australian Patent Office has recently handed down a case, N. V. Organon [2009] APO 8 (298 May 2009) which impacts the type of subject matter which is eligible for a patent term extension in Australia, particularly relating to formulations and delivery devices. The test for whether a product qualifies for a patent term extension now appears to be whether there is "integration" between the active ingredient and the other feature.

The Intellectual Property Laws Amendment Act (1998) amended the Australian Patents Act 1990 to provide, inter alia, for an extension of term for pharmaceutical patents. The scheme allows patentees to apply for an extension of term of up to 5 years for a standard patent that claims a pharmaceutical substance.

In order for a patent to be eligible for an extension, it must satisfy the criteria set out in section 70(2) of the Australian Patent Act:
  • one or more pharmaceutical substances per se must be in substance disclosed in the complete specification of the patent and in substance fall within the scope of the claim or claims of that specification, or
  • one or more pharmaceutical substances when produced by a process that involves the use of recombinant DNA technology, must in substance be disclosed in the complete specification of the patent and in substance falls within the scope of the claim or claims of that specification.
Pharmaceutical substance in the Australian Act is defined in Schedule 1 as a substance (including a mixture or compound of substances) for therapeutic use whose application (or one of whose applications) involves:
  • (a) a chemical interaction, or physico-chemical interaction, with a human physiological system; or
  • (b) action on an infectious agent, or on a toxin or other poison, in a human body;
    but does not include a substance that is solely for use in in vitro diagnosis or in in vitro testing.
In the case in question, the patentee applied for an extension of term of the patent based on its patent relating to a drug delivery system adapted to the slow release of particular steroidal mixtures such as for the purpose of contraception or hormone replacement therapy. A key aspect of the invention is that the steroidal mixture is contained in a thermoplastic polymer core over which is laid a permeable thermoplastic skin. It was considered whether the product as claimed in the patent was a pharmaceutical substance within the meaning of the Act and more particularly whether it was a substance for therapeutic use as provided in the definition given in Schedule 1.
The Commissioner held that
"the definition of a pharmaceutical substance encompasses a compound with a controlled spatial configuration if, as a whole, it can still be considered a “pharmaceutical substance”, but the combination of such a substance with what would reasonably be considered a separate physical device, layer or structure is excluded. It may be difficult to determine whether a particular feature of a product is correctly considered part of a “substance” rather than a separate physical integer but in the present case the steroidal components are mixed with and necessarily diffuse through the thermoplastic materials in the core and skin regions and as such the product as a whole exhibits a level of integration or interaction between the component parts that was considered more characteristic of a pharmaceutical substance in itself rather than a substance combined with another element or thing.
Consequently the application to extend the term of the patent was allowed. "
In its decision, the Australian Patent Office followed a line of reasoning similar to that expressed by Advocate General Leger in the ECJ MIT case.

Tuesday, 26 August 2008

Court invokes "fairness in the administration of the patent system" in rejecting late challenge to patent extension

We are grateful to Antony Taubman (WIPO) for drawing our attention to a decision of the Federal Court of Australia last week, Interpharma Pty Ltd v Commissioner of Patents [2008] FCA 1283.

In short, what happened here was that Lilly held a patent in Australia for difluro nucleoside antivirals. In 2000 Lilly sought and the Commissioner of Patents granted an extension of term for a period of five years ending in March 2009, based on the registrations in the Australian Register of Therapeutic Goods (ARTG) of the commercial product Gemcitabine hydrochloride, approved for use in the treatment of cancer of the lung and pancreas.

Interpharma objected that there was a disconformity between the product registered in the ARTG and that described in Lilly's patent specification. Accordingly Interpharma sought (i) to have the Commissioner's decision to extend the patent set aside and removed from the patent register, (ii) revocation of the patent itself and (iii) damages for false representation under the Trade Practices Act 1974. Lilly cross-claimed for infringement.

Sundberg J dismissed Interpharma's application in its entirety. The claim based on a false representation under the Trade Practices Act 1974 had to fail because that Act only applied in respect of statements made to those with whom one has, or may have, dealings in the course of commerce; this was not the relationship between Lilly and the Commissioner. Interpharma also failed to establish that it was a "person aggrieved" under the Administrative Decisions (Judicial review) Act 1977 with locus standi to challenge the Commissioner's decision since, on the facts, it was not in a position to make the patented product itself. Interpharma's application was also fatally delayed, even if allowance was made for the fact that the company was not incorporated until two years after the decision to extend the patent was taken. The judge concluded, at paragraphs 39 to 40:

"39 Another relevant matter in relation to delay is that the term of a patent is not of interest only to the patentee. As Lilly points out, it is effectively a right in rem, and of significance to all in the patent area who might be interested in trading within or near the subject matter of the patent. For this reason, the Commissioner must publish in the Official Journal a notice that an extension application has been made and is open to public inspection. If an application for extension is accepted, the Commissioner must publish a notice to that effect in the Official Journal. Provision is made for opposition proceedings. If the Commissioner grants an extension, a notice of the grant must be published in the Official Journal. ...

40 I agree with Lilly that once the opposition period has expired and an extension is granted, the patentee and third parties are prima facie entitled to proceed on the basis of the extension. Admittedly, one must take into account that the applicant was not incorporated until nearly two years after the extension. Nevertheless, the public interest to which I have referred is relevant notwithstanding that. As a matter of fairness in the administration of the patent system, it would be extraordinary if extensions could be challenged some eight years after grant. Even taking into account the applicant’s date of incorporation, it would still be extraordinary that a challenge could be made six years after that".