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Extract from the Register of European Patents

EP About this file: EP2495318

EP2495318 - PROBE FOR DETECTING MPL GENE POLYMORPHISM AND USE OF THE SAME [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  16.05.2014
Database last updated on 14.09.2024
Most recent event   Tooltip16.05.2014Application deemed to be withdrawnpublished on 18.06.2014  [2014/25]
Applicant(s)For all designated states
ARKRAY, Inc.
57, Nishiaketa-cho
Higashikujo
Minami-ku
Kyoto-shi
Kyoto 601-8045 / JP
[N/P]
Former [2012/36]For all designated states
Arkray, Inc.
57, Nishiaketa-cho Higashikujo Minami-ku Kyoto-shi
Kyoto 601-8045 / JP
Inventor(s)01 / HIRAI Mitsuharu
c/o ARKRAY, Inc.
Yousuien-nai, 59, Gansuin-cho
Kamigyo-ku
Kyoto-shi
Kyoto 602-0008 / JP
02 / KOMORI Mariko
c/o ARKRAY, Inc.
Yousuien-nai, 59, Gansuin-cho
Kamigyo-ku
Kyoto-shi
Kyoto 602-0008 / JP
 [2012/36]
Representative(s)Jones, Elizabeth Louise, et al
Dehns
St Bride's House
10 Salisbury Square
London
EC4Y 8JD / GB
[N/P]
Former [2012/36]Jones, Elizabeth Louise, et al
Dehns St Bride's House 10 Salisbury Square London
EC4Y 8JD / GB
Application number, filing date10826885.529.10.2010
WO2010JP69379
Priority number, dateJP2009025142930.10.2009         Original published format: JP 2009251429
[2012/36]
Filing languageJA
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2011052755
Date:05.05.2011
Language:JA
[2011/18]
Type: A1 Application with search report 
No.:EP2495318
Date:05.09.2012
Language:EN
[2012/36]
Search report(s)International search report - published on:JP05.05.2011
(Supplementary) European search report - dispatched on:EP10.05.2013
ClassificationIPC:C12Q1/68, C12N15/00, C12N15/09
[2013/24]
CPC:
C12Q1/6883 (EP,KR,US); C12N15/11 (KR); C12Q2600/156 (EP,KR,US)
Former IPC [2012/36]C12N15/00, C12N15/09, C12Q1/68
Designated contracting statesAL,   AT,   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,   RS,   SE,   SI,   SK,   SM,   TR [2012/36]
TitleGerman:SONDE ZUR ERKENNUNG VON POLYMORPHISMEN DES MPL-GENS UND ANWENDUNG DAVON[2012/36]
English:PROBE FOR DETECTING MPL GENE POLYMORPHISM AND USE OF THE SAME[2012/36]
French:SONDE POUR LA DÉTECTION DE POLYMORPHISME DU GÈNE MPL ET SON UTILISATION[2012/36]
Entry into regional phase29.05.2012Translation filed 
29.05.2012National basic fee paid 
29.05.2012Search fee paid 
29.05.2012Designation fee(s) paid 
29.05.2012Examination fee paid 
Examination procedure29.05.2012Examination requested  [2012/36]
10.12.2013Application deemed to be withdrawn, date of legal effect  [2014/25]
22.01.2014Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time  [2014/25]
Fees paidRenewal fee
23.10.2012Renewal fee patent year 03
Penalty fee
Additional fee for renewal fee
31.10.201304   M06   Not yet paid
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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.
Documents cited:Search[A]WO2008070370  (UNIV UTAH RES FOUND [US], et al) [A] 1-21 * example 2 * * abstract ** the whole document *;
 [XI]WO2009072084  (UNIV FIRENZE [IT], et al) [X] 1-3,6-14,20,21 * sequences 4,5 * * page 14, lines 5-6 * * page 15, line 23 - page 16, line 3 * * page 18, line 30 - line 32 * * abstract * * the whole document * [I] 4,5,15-19;
 [A]  - M. GHADERI ET AL, "Rapid real-time PCR assay for detection of MPL W515L mutation in patients with chronic myeloproliferative disorders", INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, (20081110), vol. 32, no. 1p2, doi:10.1111/j.1751-553X.2008.01118.x, ISSN 1751-5521, pages 122 - 126, XP055061379 [A] 1-21 * table 1 * * abstract * * the whole document *

DOI:   http://dx.doi.org/10.1111/j.1751-553X.2008.01118.x
International search[Y]WO2008084672  (ARKRAY INC [JP], et al);
 [A]CN101403009  (PEOPLE S HOSPITAL OF BEIJING [CN]);
 [X]WO2009072084  (UNIV FIRENZE [IT], et al);
 [Y]  - KAZUTAKA NAKAYAMA ET AL., "Kotsuzui Zoshokusei Shuyo ni Okeru JAK2 exon12 no Hen'i to c- MPLW515L/K Hen'i no Shinki Kenshutsuho no Kaihatsu", RINSHO KETSUEKI, (20090930), vol. 50, no. 9, page 939
 [Y]  - PARDANANI, A., D. ET AL., "MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients", BLOOD, (2006), vol. 108, doi:doi:10.1182/blood-2006-04-018879, pages 3472 - 3476, XP009117093

DOI:   http://dx.doi.org/10.1182/blood-2006-04-018879
 [XP]  - RUAN, G., R. ET AL., "MPL W515L/K mutations in 343 Chinese adults with JAK2V617F mutation- negative chronic myeloproliferative disorders detected by a newly developed RQ-PCR based on TaqMan MGB probes", HEMATOL. ONCOL., (2010), vol. 28, pages 33 - 39
by applicantUS4889818
 WO9109950
 EP0455430
 US5079352
 WO9209689
 JP2009251429
    - PARADANANI ET AL., BLOOD, (2006), vol. 108, no. 10, pages 3472 - 3476
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.