G 0002/08 (Dosage regime/ABBOTT RESPIRATORY) vom 19.02.2010
- Europäischer Rechtsprechungsidentifikator
- ECLI:EP:BA:2010:G000208.20100219
- Datum der Entscheidung
- 19. Februar 2010
- Aktenzeichen
- G 0002/08
- Antrag auf Überprüfung von
- -
- Anmeldenummer
- 94306847.8
- IPC-Klasse
- A61K 31/445
- Verfahrenssprache
- Englisch
- Verteilung
- Im Amtsblatt des EPA veröffentlicht (A)
- Download
- Entscheidung auf Englisch
- Amtsblattfassungen
- Weitere Entscheidungen für diese Akte
- G 0002/08 2009-06-15
- Zusammenfassungen für diese Entscheidung
- -
- Bezeichnung der Anmeldung
- Nicotinic acid compositions for treating hyperlipidemia
- Name des Antragstellers
- Abbott Respiratory LLC
- Name des Einsprechenden
- -
- Kammer
- -
- Leitsatz
The questions referred to the Enlarged Board of Appeal are answered as follows:
Question 1: Where it is already known to use a medicament to treat an illness, Article 54(5) EPC does not exclude that this medicament be patented for use in a different treatment by therapy of the same illness.
Question 2: Such patenting is also not excluded where a dosage regime is the only feature claimed which is not comprised in the state of the art.
Question 3: Where the subject matter of a claim is rendered novel only by a new therapeutic use of a medicament, such claim may no longer have the format of a so called Swiss-type claim as instituted by decision G 5/83.
A time-limit of three months after publication of the present decision in the Official Journal of the European Patent Office is set in order that future applicants comply with this new situation.
- Relevante Rechtsnormen
- Court of Appeal (UK) of 21 May 2008 in re Actavis UK Limited v. Merck & Co. Inc, (2008) EWCA Civ 444European Patent Convention Art 52(4) 1973European Patent Convention Art 53(c)European Patent Convention Art 54(4)European Patent Convention Art 54(5)European Patent Convention Art 54(5) 1973German Federal Court of Justice: BGH, 19 December 2006, XZR 236/01 "Carvedilol IITribunal of Commerce of the Canton of Zurich, decisions of 14 April 2009, AA 090075 and AA 090077Vienna Convention on the Law of Treaties (1969) Art 31Vienna Convention on the Law of Treaties (1969) Art 32
- Schlagwörter
- Admissibility of referral (yes)
Applicable law
Rules of interpretation of the EPC as an international treaty
Respective domains of prohibition under Art. 53(c) EPC and permission under Art. 54(4) and (5) EPC)
Intention of the legislator
Notional novelty concept under Art. 54(4) and (5) EPC
Meaning of any "specific use" under Art. 54(5) EPC
Technical effect of a specific use
Abolition of so called Swiss-type claims
Time limit set for applicants to comply - Orientierungssatz
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- Zitierte Akten
- G 0005/83G 0001/04G 0001/07T 0116/85T 0019/86T 0290/86T 0182/90T 0893/90T 0820/92T 0051/93T 0082/93T 0254/93T 0138/95T 0233/96T 0836/01T 1020/03T 0406/06T 1074/06
- Zitierende Akten
- G 0003/08G 0001/09G 0002/12G 0002/13G 0001/18G 0003/19G 0001/21G 0002/21R 0012/09R 0002/12R 0019/12R 0002/14T 1319/04T 1283/05T 0578/06T 0795/06T 0826/06T 1242/06T 1918/06T 0047/07T 0294/07T 0566/07T 1827/07T 1760/08T 1838/08T 2003/08T 0108/09T 1046/09T 1075/09T 1099/09T 1138/09T 1570/09T 1627/09T 1635/09T 1955/09T 0773/10T 2369/10T 0524/11T 0677/11T 1021/11T 1069/11T 1554/11T 1577/11T 1673/11T 1760/11T 1869/11T 0734/12T 1184/12T 1780/12T 2017/12T 2473/12T 2506/12T 0177/13T 0714/13T 0943/13T 1819/13T 1889/13T 0013/14T 0015/14T 0799/14T 0899/14T 1758/15T 1824/15T 0664/16T 0694/16T 0857/16T 1186/16T 2440/16T 2707/16T 1243/17T 1991/17T 0779/18T 1287/18T 1345/18T 1732/18T 0339/19T 0634/19T 0935/19T 0968/19T 1868/19T 2360/19T 2516/19T 2689/19T 2805/19T 0468/20T 0558/20T 1252/20T 1047/21T 1356/21T 1357/21T 1863/21T 0160/22T 0295/22T 0815/22T 1259/22T 1390/22T 2012/22T 0278/23T 0867/23T 1874/23T 0197/24T 0792/24
ORDER
For these reasons it is decided that:
The questions referred to the Enlarged Board of Appeal are answered as follows:
Question 1:
Where it is already known to use a medicament to treat an illness, Article 54(5) EPC does not exclude that this medicament be patented for use in a different treatment by therapy of the same illness.
Question 2:
Such patenting is also not excluded where a dosage regime is the only feature claimed which is not comprised in the state of the art.
Question 3:
Where the subject matter of a claim is rendered novel only by a new therapeutic use of a medicament, such claim may no longer have the format of a so called Swiss-type claim as instituted by decision G 5/83.
A time-limit of three months after publication of the present decision in the Official Journal of the European Patent Office is set in order that future applicants comply with this new situation.