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Extract from the Register of European Patents

EP About this file: EP2245185

EP2245185 - A MUTATION IN THE REGULATORY REGION OF GJB2 MEDIATES NEONATAL HEARING LOSS WITHIN DFNB1 [Right-click to bookmark this link]
StatusNo opposition filed within time limit
Status updated on  06.03.2015
Database last updated on 24.08.2024
Most recent event   Tooltip22.06.2018Lapse of the patent in a contracting state
New state(s): MK
published on 25.07.2018  [2018/30]
Applicant(s)For all designated states
Med-El Elektromedizinische Geräte GmbH
Fürstenweg 77a
6020 Innsbruck / AT
[2010/44]
Inventor(s)01 / LUCAS, Trevor
Wurmsergasse 28/18
A-1150 Vienna / AT
02 / FREI, Klemens
Dr. Weinbrennerstrasse 63
A-2103 Langenzersdorf / AT
03 / BAUMGARTNER, Wolf-Dieter
Ebenberg 2
A-2500 Sicgenfeld / AT
 [2010/44]
Representative(s)Hutter, Anton, et al
Venner Shipley LLP
5 Stirling House
Stirling Road The Surrey Research Park
Guildford GU2 7RF / GB
[N/P]
Former [2014/18]Hutter, Anton, et al
Venner Shipley LLP
200 Aldersgate
London EC1A 4HD / GB
Former [2010/44]Hutter, Anton, et al
Venner Shipley LLP 20 Little Britain London
EC1A 7DH / GB
Application number, filing date09712932.419.02.2009
[2010/44]
WO2009US34523
Priority number, dateUS2008006614619.02.2008         Original published format: US 66146
[2010/44]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2009105543
Date:27.08.2009
Language:EN
[2009/35]
Type: A1 Application with search report 
No.:EP2245185
Date:03.11.2010
Language:EN
The application published by WIPO in one of the EPO official languages on 27.08.2009 takes the place of the publication of the European patent application.
[2010/44]
Type: B1 Patent specification 
No.:EP2245185
Date:30.04.2014
Language:EN
[2014/18]
Search report(s)International search report - published on:EP27.08.2009
ClassificationIPC:C12Q1/68
[2010/44]
CPC:
C12Q1/6883 (EP,US); C12Q2600/156 (EP,US); C12Q2600/16 (EP,US)
Designated contracting statesAT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   LV,   MC,   MK,   MT,   NL,   NO,   PL,   PT,   RO,   SE,   SI,   SK,   TR [2010/44]
TitleGerman:MUTATION IM REGULATORISCHEN BEREICH VON GJB2 ALS VERMITTLER VON NEONATALEM GEHÖRVERLUST IN DFNB1[2010/44]
English:A MUTATION IN THE REGULATORY REGION OF GJB2 MEDIATES NEONATAL HEARING LOSS WITHIN DFNB1[2010/44]
French:UNE MUTATION DANS LA RÉGION RÉGULATRICE DU GÈNE GJB2 RESPONSABLE DE SURDITÉ NÉONATALE AU SEIN DE DFNB1[2010/44]
Entry into regional phase17.08.2010National basic fee paid 
17.08.2010Designation fee(s) paid 
17.08.2010Examination fee paid 
Examination procedure17.08.2010Examination requested  [2010/44]
16.11.2010Amendment by applicant (claims and/or description)
12.01.2012Despatch of a communication from the examining division (Time limit: M04)
22.05.2012Reply to a communication from the examining division
08.11.2012Despatch of a communication from the examining division (Time limit: M06)
15.05.2013Reply to a communication from the examining division
14.11.2013Communication of intention to grant the patent
18.03.2014Fee for grant paid
18.03.2014Fee for publishing/printing paid
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  12.01.2012
Opposition(s)02.02.2015No opposition filed within time limit [2015/15]
Fees paidRenewal fee
23.02.2011Renewal fee patent year 03
24.02.2012Renewal fee patent year 04
07.02.2013Renewal fee patent year 05
07.02.2014Renewal fee patent year 06
Opt-out from the exclusive  Tooltip
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See the Register of the Unified Patent Court for opt-out data
Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Lapses during opposition  TooltipHU19.02.2009
AT30.04.2014
BE30.04.2014
CY30.04.2014
CZ30.04.2014
DK30.04.2014
EE30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
IT30.04.2014
LT30.04.2014
LV30.04.2014
MC30.04.2014
MK30.04.2014
MT30.04.2014
NL30.04.2014
PL30.04.2014
RO30.04.2014
SE30.04.2014
SI30.04.2014
SK30.04.2014
TR30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
[2018/30]
Former [2017/39]HU19.02.2009
AT30.04.2014
BE30.04.2014
CY30.04.2014
CZ30.04.2014
DK30.04.2014
EE30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
IT30.04.2014
LT30.04.2014
LV30.04.2014
MC30.04.2014
MT30.04.2014
NL30.04.2014
PL30.04.2014
RO30.04.2014
SE30.04.2014
SI30.04.2014
SK30.04.2014
TR30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2017/03]AT30.04.2014
BE30.04.2014
CY30.04.2014
CZ30.04.2014
DK30.04.2014
EE30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
IT30.04.2014
LT30.04.2014
LV30.04.2014
MC30.04.2014
MT30.04.2014
NL30.04.2014
PL30.04.2014
RO30.04.2014
SE30.04.2014
SI30.04.2014
SK30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2015/46]AT30.04.2014
BE30.04.2014
CY30.04.2014
CZ30.04.2014
DK30.04.2014
EE30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
IT30.04.2014
LT30.04.2014
LV30.04.2014
MC30.04.2014
NL30.04.2014
PL30.04.2014
RO30.04.2014
SE30.04.2014
SI30.04.2014
SK30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2015/36]AT30.04.2014
BE30.04.2014
CY30.04.2014
CZ30.04.2014
DK30.04.2014
EE30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
IT30.04.2014
LT30.04.2014
LV30.04.2014
NL30.04.2014
PL30.04.2014
RO30.04.2014
SE30.04.2014
SI30.04.2014
SK30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2015/18]AT30.04.2014
BE30.04.2014
CY30.04.2014
CZ30.04.2014
DK30.04.2014
EE30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
IT30.04.2014
LT30.04.2014
LV30.04.2014
NL30.04.2014
PL30.04.2014
RO30.04.2014
SE30.04.2014
SK30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2015/11]AT30.04.2014
BE30.04.2014
CY30.04.2014
CZ30.04.2014
DK30.04.2014
EE30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
LT30.04.2014
LV30.04.2014
NL30.04.2014
PL30.04.2014
RO30.04.2014
SE30.04.2014
SK30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2015/10]AT30.04.2014
BE30.04.2014
CY30.04.2014
CZ30.04.2014
DK30.04.2014
EE30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
LT30.04.2014
LV30.04.2014
NL30.04.2014
PL30.04.2014
SE30.04.2014
SK30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2015/08]AT30.04.2014
BE30.04.2014
CY30.04.2014
DK30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
LT30.04.2014
LV30.04.2014
NL30.04.2014
PL30.04.2014
SE30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2015/02]AT30.04.2014
CY30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
LT30.04.2014
LV30.04.2014
NL30.04.2014
PL30.04.2014
SE30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
PT01.09.2014
Former [2014/51]AT30.04.2014
CY30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
LT30.04.2014
LV30.04.2014
NL30.04.2014
PL30.04.2014
SE30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
Former [2014/50]CY30.04.2014
ES30.04.2014
FI30.04.2014
HR30.04.2014
LT30.04.2014
LV30.04.2014
NL30.04.2014
PL30.04.2014
SE30.04.2014
BG30.07.2014
NO30.07.2014
GR31.07.2014
IS30.08.2014
Former [2014/49]CY30.04.2014
FI30.04.2014
LT30.04.2014
BG30.07.2014
NO30.07.2014
IS30.08.2014
Former [2014/48]CY30.04.2014
LT30.04.2014
BG30.07.2014
Former [2014/47]CY30.04.2014
Cited inInternational search[X]US2004203035  (MAST ANDREA L [US], et al) [X] 1-21 * page 1 - page 11 *;
 [X]  - KALAY E ET AL, "GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations", HEARING RESEARCH, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, (20050501), vol. 203, no. 1-2, ISSN 0378-5955, pages 88 - 93, XP004868112 [X] 1-21 * page 88 - page 92 *

DOI:   http://dx.doi.org/10.1016/j.heares.2004.11.022
 [X]  - FINSTERER J ET AL, "Nuclear and mitochondrial genes mutated in nonsyndromic impaired hearing", INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, ELSEVIER, AMSTERDAM, NL, (20050501), vol. 69, no. 5, ISSN 0165-5876, pages 621 - 647, XP004858013 [X] 1-21 * page 621 - page 635 * * page 637 - page 638 *

DOI:   http://dx.doi.org/10.1016/j.ijporl.2004.12.002
 [A]  - SMITH ET AL, "Relationships between neurologic disorders and hereditary hearing loss", SEMINARS IN PEDIATRIC NEUROLOGY, SAUNDERS, PHILADELPHIA, PA, US, (20010901), vol. 8, no. 3, ISSN 1071-9091, pages 147 - 159, XP005468052 [A] 1-21 * the whole document *

DOI:   http://dx.doi.org/10.1053/spen.2001.26448
Examination   - CARYN ROTHROCK ET AL, "Connexin 26 35delG does not represent a mutational hotspot.", HUMAN GENETICS, (20030701), vol. 113, no. 1, doi:10.1007/s00439-003-0944-2, ISSN 0340-6717, pages 18 - 23, XP055015706

DOI:   http://dx.doi.org/10.1007/s00439-003-0944-2
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.