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Extract from the Register of European Patents

EP About this file: EP1853249

EP1853249 - A STABLE PHARMACEUTICAL COMPOSITION COMPRISING A FIXED DOSE COMBINATION OF FENOFIBRATE AND AN HMG-COA REDUCTASE INHIBITOR [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  03.01.2014
Database last updated on 14.06.2024
Most recent event   Tooltip03.01.2014Application deemed to be withdrawnpublished on 05.02.2014  [2014/06]
Applicant(s)For all designated states
Veloxis Pharmaceuticals A/S
Kogle Alle 4
2970 Ho̸rsholm / DK
[2011/34]
Former [2007/46]For all designated states
LifeCycle Pharma A/S
Kogle Alle 4
2970 Horsholm / DK
Inventor(s)01 / HOLM, Per
Gro̸ndals Parkvej 54
DK-2720 Vanlo̸se / DK
02 / NORLING, Tomas
Mo̸llevænget 36
DK-2800 Lyngby / DK
 [2007/46]
Representative(s)Grünecker Patent- und Rechtsanwälte PartG mbB
Leopoldstrasse 4
80802 München / DE
[N/P]
Former [2008/28]Grünecker, Kinkeldey, Stockmair & Schwanhäusser Anwaltssozietät
Leopoldstrasse 4
80802 München / DE
Former [2007/46]Joersboe, Anne-Marie Charlotte H.
LifeCycle Pharma A/S Kogle Allé 4
2970 Harsholm / DK
Application number, filing date06706137.410.02.2006
[2007/46]
WO2006DK50004
Priority number, dateDK2005000020010.02.2005         Original published format: DK 200500200
DK2005000057620.04.2005         Original published format: DK 200500576
[2007/46]
Filing languageEN
Procedural languageEN
PublicationType: A2 Application without search report
No.:WO2006084474
Date:17.08.2006
Language:EN
[2006/33]
Type: A2 Application without search report 
No.:EP1853249
Date:14.11.2007
Language:EN
The application published by WIPO in one of the EPO official languages on 17.08.2006 takes the place of the publication of the European patent application.
[2007/46]
Search report(s)International search report - published on:EP02.11.2006
ClassificationIPC:A61K31/216, A61K31/366, A61K31/40, A61K9/16, A61K9/24, A61K9/26
[2007/46]
CPC:
A61K45/06 (EP,US); A61K9/20 (KR); A61K31/216 (EP,US);
A61K31/366 (EP,US); A61K31/40 (EP,KR,US); A61K9/16 (KR);
A61K9/209 (EP,KR,US); A61P43/00 (EP) (-)
C-Set:
A61K31/216, A61K2300/00 (EP,US);
A61K31/366, A61K2300/00 (US,EP);
A61K31/40, A61K2300/00 (US,EP)
Designated contracting statesAT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   LV,   MC,   NL,   PL,   PT,   RO,   SE,   SI,   SK,   TR [2007/46]
Extension statesAL10.09.2007
BA10.09.2007
HR10.09.2007
MK10.09.2007
YU10.09.2007
TitleGerman:STABILE PHARMAZEUTISCHE ZUSAMMENSETZUNG AUS EINER FIXDOSEN-KOMBINATION VON FENOFIBRAT UND EINEM HMG-COA-REDUCTASE-HEMMER[2007/46]
English:A STABLE PHARMACEUTICAL COMPOSITION COMPRISING A FIXED DOSE COMBINATION OF FENOFIBRATE AND AN HMG-COA REDUCTASE INHIBITOR[2007/46]
French:PREPARATION PHARMACEUTIQUE STABLE COMPRENANT UNE DOSE FIXE DE FENOFIBRATE ET D'UN INHIBITEUR DE LA HMG-COA REDUCTASE[2007/46]
Entry into regional phase10.09.2007National basic fee paid 
10.09.2007Designation fee(s) paid 
10.09.2007Examination fee paid 
Examination procedure28.08.2007Amendment by applicant (claims and/or description)
10.09.2007Examination requested  [2007/46]
20.12.2007Despatch of a communication from the examining division (Time limit: M08)
16.12.2008Reply to a communication from the examining division
19.01.2009Despatch of a communication from the examining division (Time limit: M06)
10.11.2009Reply to a communication from the examining division
03.09.2013Application deemed to be withdrawn, date of legal effect  [2014/06]
27.09.2013Despatch of communication that the application is deemed to be withdrawn, reason: renewal fee not paid in time  [2014/06]
Divisional application(s)The date of the Examining Division's first communication in respect of the earliest application for which a communication has been issued is  20.12.2007
Request for further processing for:The application is deemed to be withdrawn due to failure to reply to the examination report
16.12.2008Request for further processing filed
16.12.2008Full payment received (date of receipt of payment)
Request granted
07.01.2009Decision despatched
Fees paidRenewal fee
29.02.2008Renewal fee patent year 03
02.03.2009Renewal fee patent year 04
01.03.2010Renewal fee patent year 05
28.02.2011Renewal fee patent year 06
29.02.2012Renewal fee patent year 07
Penalty fee
Additional fee for renewal fee
28.02.201308   M06   Not yet paid
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Cited inInternational search[E]WO2006037348  (LIFECYCLE PHARMA AS [DK], et al) [E] 1-48,1-48,1-48 * paragraph [0293] - paragraph [0310] * * paragraph [0319] - paragraph [0369] * * paragraph [0293] - paragraph [0310] * * paragraph [0319] - paragraph [0369] * * paragraph [0293] - paragraph [0310] * * paragraph [0319] - paragraph [0369] *;
 [E]WO2006037344  (LIFECYCLE PHARMA AS [DK], et al) [E] 1-48,1-48,1-48 * paragraph [0289] - paragraph [0306] * * paragraph [0317] - paragraph [0347] * * paragraph [0289] - paragraph [0306] * * paragraph [0317] - paragraph [0347] * * paragraph [0289] - paragraph [0306] * * paragraph [0317] - paragraph [0347] *;
 [X]WO0037078  (BAYER AG [DE], et al) [X] 1-48,1-48,1-48 * examples 3,4 * * examples 3,4 * * examples 3,4 *;
 [X]EP0455042  (SQUIBB & SONS INC [US]) [X] 1-48,1-48,1-48 * page 5, lines 27,28 * * page 5, lines 27,28 * * page 5, lines 27,28 *;
 [X]EP0475148  (SQUIBB & SONS INC [US]) [X] 1-48,1-48,1-48 * example 3 * * example 3 * * example 3 *;
 [X]WO03013608  (GALEPHAR M F [BE], et al) [X] 1-48,1-48,1-48 * example 3 * * example 3 * * example 3 *;
 [X]WO0224169  (RTP PHARMA INC [US]) [X] 1-48,1-48,1-48 * page 53, line 8 - line 9 * * page 53, line 27 * * page 54, line 9 * * page 55, line 23 - line 25 * * page 53, line 8 - line 9 * * page 53, line 27 * * page 54, line 9 * * page 55, line 23 - line 25 * * page 53, line 8 - line 9 * * page 53, line 27 * * page 54, line 9 * * page 55, line 23 - line 25 *
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.