A decision (T1780/12) from the EPO technical boards of appeal
indicates that Swiss-type claims of the form "Use of [product
X] in the manufacture of a medicament for the treatment of [disease
Y]" provide a different scope of protection than EPC 2000
second medical use claims of the form "[product X] for use in
the treatment of [disease Y]". Swiss-type claims are widely
used in European patents directed to new medical indications of
known compounds, so this decision could have important implications
for the enforcement of many patents in the national courts across
Europe.
For policy reasons, European patent law has long prohibited the patenting of methods of medical treatment on the human or animal body. By way of compensation, the law allows for the patenting of known substances or compositions by reference to their first use in any method of medical treatment. This is an exception to the normal principle of European patent law that the intended use of a product does not usually confer novelty to that product. However, the old EPC 1973 made no specific reference to further medical uses of existing compounds already known for a medical use. Instead, it had become established practice to claim further medical indications using the Swiss-type claim format set out above.
On the 13th December 2007, the EPC 2000 rectified this situation
by introducing specific protection for further medical uses of
known products, under new Article 54(5) EPC, via claims drafted in
the form "[product X] for use in the treatment of [disease
Y]". It was the intention of the legislator that this new form
of claim would afford equivalent protection to that of the previous
Swiss-type claim. However, doubts remained on a national level
about whether or not the intention of the legislator had been
fulfilled and this has now been explicitly challenged by the EPO
technical boards of appeal in the decision T1780/12.
T1780/12 concerned a case of double patenting. The applicant
already owned a granted patent (EP1) containing a Swiss-type claim.
They also applied for a divisional application (EP2) containing an
EPC 2000 second medical use claim for the same substance and
medical indication.
The Examining Division refused EP2 for double patenting, because
it considered that an EPC 2000 second medical use claim is directed
to the same subject matter as a corresponding Swiss-type claim.
They stated that the intention of the EPC legislator was that the
two claim formats were equivalent and dismissed the applicant's
arguments that the differing scope of the respective claims was
relevant.
The Board of Appeal in question disagreed with the Examining
Division, reasoning that the subject matter of a claim is
determined by its technical features and its category (i.e. whether
it is a claim to a product, process, apparatus or use). Considering
the categories of the respective claims, the Board held that claim
1 of EP1 (a Swiss-type claim) was a purpose-limited
process claim, whereas claim 1 of EP2 (an EPC 2000 second
medical use claim) was a purpose-limited product claim. It
followed directly from this that the subject matter of the two
claims was different and so the grant of EP2 could not be prevented
for double patenting vis-à-vis EP1.
The Board went further and concluded that the difference in
subject matter led to a variance in the protection afforded by both
formats of claim. According to the Board, since a claim to a
particular physical activity (e.g. a method, process or use)
confers less protection than a claim to the physical entity per
se, it followed that a purpose-limited process claim (i.e. a
Swiss-type claim) confers less protection than a purpose-limited
product claim (i.e. an EPC 2000 second medical use claim).
It is interesting to see an EPO Board of Appeal reach this
conclusion, because it goes against the intention of the legislator
that EPC 2000 second-medical use claims should afford equivalent
protection to that of Swiss-type claims. The Board made a point to
highlight that it was only the intention of the legislator
that the scope of the claims should be the same and it clearly
thought that the intention had not been achieved in practice.
From an enforcement perspective, the scope of protection of
these claims may not be the only difference. The UK Patents Act
defines the meaning of infringement differently where the invention
is a product compared to a process. Given that the EPO boards of
appeal have explicitly classified Swiss-type claims as process
claims and EPC 2000 second medical use claims as product claims,
this could lead to a divergence in the enforcement of EPC 2000
second medical use claims and Swiss-type claims under the UK
Patents Act and potentially the national law of other European
states.
Following the Board's logic, an EPC 2000 second medical use
product claim would be directly infringed by dealings in the
product itself (though it would also be necessary to show that the
product was intended for use in the specified medical treatment).
However, by the same logic, a Swiss-type process claim would only
be directly infringed by manufacturing the claimed medicament in
the UK, or in dealing with the medicament obtained directly by
means of the claimed process. Quite how this distinction will
manifest itself in practice will be a matter of great interest to
those in the pharmaceutical sector.
As such, we continue to recommend that EPC 2000 second medical use claims are included in pending applications wherever possible, alongside Swiss-type claims. For granted patents, it is unlikely that Swiss-type claims can be converted into EPC 2000 second medical use claims, because, according to the Board, this would lead to an impermissible extension of the scope of protection afforded by the patent. However, where a pending divisional application exists, T1780/12 provides comfort that EPC 2000 second medical use claims pursued in the divisional would not conflict for double patenting with a corresponding Swiss-type claim in a granted parent patent.
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Carpmaels & Ransford LLP is a leading firm of European patent and trade mark attorneys based in London. For more information about our firm and our practice, please visit our website at www.carpmaels.com.
This Briefing Note was first published in the IAM IP Newsletter.
The content of this article is intended to provide a general guide to the subject matter. Specialist advice should be sought about your specific circumstances.