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Extract from the Register of European Patents

EP About this file: EP1729766

EP1729766 - PHARMACEUTICAL FORMULATION [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  03.01.2014
Database last updated on 24.08.2024
Most recent event   Tooltip03.01.2014Application deemed to be withdrawnpublished on 05.02.2014  [2014/06]
Applicant(s)For all designated states
LEK Pharmaceuticals d.d.
Verovskova 57
1526 Ljubljana / SI
[2010/10]
Former [2006/50]For all designated states
LEK Pharmaceuticals d.d.
Verovskova 57
1526 Ljubljana / SI
Inventor(s)01 / SVETE, Peter
Gradisnikova 14
1353 Borovnica / SI
02 / GRAHEK, Rok
Zoisova 17
4000 Kranj / SI
03 / HUMAR, Vlasta
Godic 63
1242 Stahovica / SI
04 / HUSU-KOVACEVIC, Breda
Na peci 27
1000 Ljubljana / SI
05 / JERALA-STRUKELJ, Zdenka
Podreca 107
4211 Mavcice / SI
 [2006/50]
Representative(s)Prüfer & Partner mbB Patentanwälte Rechtsanwälte
Sohnckestrasse 12
81479 München / DE
[N/P]
Former [2012/14]Prüfer & Partner GbR European Patent Attorneys
Sohnckestrasse 12
81479 München / DE
Former [2010/10](deleted)
Former [2008/25]Kröger, Bernd, et al
Sandoz International GmbH Global Patents Department Industriestrasse 25
83607 Holzkirchen / DE
Former [2006/50]Skulj, Primoz, et al
Novartis AG Corporate Intellectual Property
4002 Basel / CH
Application number, filing date05707662.228.02.2005
[2006/50]
WO2005EP02108
Priority number, dateSI2004000006701.03.2004         Original published format: SI 200400067
[2006/50]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2005084670
Date:15.09.2005
Language:EN
[2005/37]
Type: A1 Application with search report 
No.:EP1729766
Date:13.12.2006
Language:EN
The application published by WIPO in one of the EPO official languages on 15.09.2005 takes the place of the publication of the European patent application.
[2006/50]
Search report(s)International search report - published on:EP15.09.2005
ClassificationIPC:A61K31/4184, A61K31/695, A61K9/28, C07D403/10
[2006/50]
CPC:
A61K31/4174 (EP); A61K9/28 (US); A61K31/4184 (US);
A61K31/695 (US); A61K9/2009 (EP); A61K9/282 (EP);
A61K9/2853 (EP); C07D403/10 (EP,US) (-)
Designated contracting statesAT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   MC,   NL,   PL,   PT,   RO,   SE,   SI,   SK,   TR [2006/50]
Extension statesALNot yet paid
BANot yet paid
HRNot yet paid
LVNot yet paid
MKNot yet paid
YUNot yet paid
TitleGerman:PHARMAZEUTISCHE FORMULIERUNG[2006/50]
English:PHARMACEUTICAL FORMULATION[2006/50]
French:FORMULATION PHARMACEUTIQUE[2006/50]
Entry into regional phase02.10.2006National basic fee paid 
02.10.2006Designation fee(s) paid 
02.10.2006Examination fee paid 
Examination procedure15.12.2005Request for preliminary examination filed
International Preliminary Examining Authority: EP
02.10.2006Examination requested  [2006/50]
15.11.2007Despatch of a communication from the examining division (Time limit: M04)
22.11.2007Observations by third parties
27.06.2008Reply 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  15.11.2007
Request for further processing for:The application is deemed to be withdrawn due to failure to reply to the examination report
27.06.2008Request for further processing filed
27.06.2008Full payment received (date of receipt of payment)
Fees paidRenewal fee
28.02.2007Renewal fee patent year 03
13.02.2008Renewal fee patent year 04
13.02.2009Renewal fee patent year 05
16.02.2010Renewal fee patent year 06
15.02.2011Renewal fee patent year 07
15.02.2012Renewal fee patent year 08
Penalty fee
Additional fee for renewal fee
28.02.201309   M06   Not yet paid
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Cited inInternational search[A]US5140037  (CHIU ANDREW T [US], et al) [A] 1-17* the whole document *;
 [X]US5225202  (HODGES GARRY R [GB], et al) [X] 1,11 * column 3 - column 4; examples 1,2; claims 15,18,20,23,29,30 *;
 [X]WO9517396  (MERCK & CO INC [US], et al) [X] 1-17 * page 1 * * page 38 - page 42; claim 1 *;
 [X]US5962500  (EIDE IVAR K [US], et al) [X] 1,11-13 * column 29 *;
 [A]WO0193859  (LEK TOVARNA FARMACEVTSKIH [SI], et al) [A] 1-17 * page 3 - page 6 * * page 16 - page 18 *;
 [A]WO02094816  (AUROBINDO PHARMA LTD [IN]) [A] 1-4,11-13 * the whole document *;
 [XD]WO03048135  (TEVA PHARMA [IL], et al) [XD] 1-17 * paragraphs [0007] , [0077] - [0087] - [0114] - [0128] *
otherEP0546358
    - WATANABE T; ET AL, "Stability of amorphous indomethacin compounded with silica", INTERNATIONAL JOURNAL OF PHARMACEUTICS, (2001), vol. 226, pages 81 - 91, XP002310637

DOI:   http://dx.doi.org/10.1016/S0378-5173(01)00776-1
    - BAUER K.H. ET AL., Pharmazeutische Technologie, 4e Auflage, GEORG THIEME VERLAG, (1993), XP003017486
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.