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No. 180 Managing Intell. Prop. 82 (2008)
A Brief History of Swiss-type Claims

handle is hein.journals/manintpr180 and id is 82 raw text is: 
IndustryFocus: SPONSORED EDITORIAL


Changes to European patent law have brought an end to the need for Swiss-type claims. Bdatrice
Holtz and Lionel Vial of Lavoix explain what replaces them




A brief history of Swiss-type claims


      he patentability of therapeutic substances or composi-
      tions was initially defined in Article 54.5 of the 1973
      version of the European Patent Convention (EPC).
The patentability of substances or compositions comprised
in the state of the art for use in methods of treating the
human or animal body by surgery or therapy was not
excluded, provided that their use for any of such methods
was not comprised in the state of the art (see table). In other
words, EPC 1973 authorized patents on a first medical indi-
cation of known substances or compositions. Strictly inter-
preted, it could also forbid patentability of second (or fur-
ther) medical indications.
   However, taking the importance for the pharmaceutical
industry, of such a protection into consideration, the
Enlarged Board of Appeal (EBA) of the European Patent
Office (EPO) gave another, less strict, interpretation of
Article 54(5) EPC 1973 in its famous Second Medical
Indication Decision, G 5/83 of December 5 1984. The EBA
considered that Article 54(5) EPC 1973 merely excluded
claims relating to second (or further) medical indications
from being drafted as purpose-limited product claims; no
intention to exclude such indications generally from patent
protection could be deduced from the terms of the EPC. As
a consequence, the EBA, adopting a practice followed by
the Swiss Federal Intellectual Property Office, found it legit-
imate to allow claims directed to the use of a substance or
composition for the manufacture of a medicament for a
specified new and inventive therapeutic application, thereby
paving the way for the worldwide success of so-called
Swiss-type claims.
   More recently, the situation was clarified with the revised
version of the EPC (EPC 2000), which entered into force in
December 13 2007. Article 54(5) EPC 2000 (see table) now
explicitly establishes protection of second (or further) medical
indications, rendering the Swiss-type circumlocution unneces-
sary for prosecuting European patent applications.


Beatrice Holtz
               After obtaining her PhD in biochemistry in
               2000 from the Institut National
               Agronomique Paris-Grignon, Beatrice
               Holtz joined Lavoix in 2001, becoming
               partner in 2007. As a French and
               European patent attorney, her specialism
               includes drafting and prosecuting patent
               applications, filing Supplementary
Protection Certificates, conducting patentability and free-
dom-to-operate opinions, and prosecuting opposition and
appeal procedures. She is also involved in patent litigation.






Lionel Vial
               Lionel Vial graduated from the Ecole
               Normale Superieure de Cachan in 1998
               and holds a PhD in biochemistry and
               molecular biology from the Ecole
               Polytechnique (2002). He joined Lavoix in
               2005 after three years of practice at
               another IP firm where he worked in
               biotechnology. He has been a European
patent attorney since 2006. His areas of practice mainly
focus on drafting and prosecuting patent applications,
patentability and freedom-to-operate opinions, and opposi-
tion procedures.


      A first consequence of the changes brought by EPC 2000 is formal. What form
      should now be adopted claims relating to second (or further) medical indications?
      The current version of the Guidelines for Examination in the EPO (published in
      December 2007) remains silent on that point, still only referring to Swiss-type
      claims. But the first post-EPC 2000 decision relating to second medical indications
      from a Board of Appeal of the EPO (T1127/05 - 3.3.4 of January 15 2008) gives an
      example of a purpose-limited product claim deemed acceptable:
        An ov3 antagonist for inhibiting 0vf33-mediated angiogenesis in a tissue, where-
        in said antagonist is an organic mimetic compound having a structure according
        to formula 7, 9, 10, 12 or 14.








8 2   www.managingip.com
      June 2008

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