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Extract from the Register of European Patents

EP About this file: EP2509974

EP2509974 - PYRAZOLES DERIVATIVES MODULATORS OF CALCIUM RELEASE-ACTIVATED CALCIUM CHANNEL AND METHODS FOR TREATMENT OF NON-SMALL CELL LUNG CANCER [Right-click to bookmark this link]
Former [2012/42]PYRAZOLES DERIVATIVES MODULATORS OF CALCIUM RELEASE -ACTIVATED CALCIUM CHANNEL AND METHODS FOR TREATMENT OF NON- SMALL CELL LUNG CANCER
[2017/47]
StatusNo opposition filed within time limit
Status updated on  15.02.2019
Database last updated on 17.07.2024
FormerThe patent has been granted
Status updated on  09.03.2018
FormerGrant of patent is intended
Status updated on  30.10.2017
FormerExamination is in progress
Status updated on  08.02.2017
Most recent event   Tooltip15.02.2019No opposition filed within time limitpublished on 20.03.2019  [2019/12]
Applicant(s)For all designated states
Rhizen Pharmaceuticals S.A.
Fritz Courvoisier 40
2300 La Chaux de Fonds / CH
[2012/42]
Inventor(s)01 / MUTHUPPALANIAPPAN, Meyyappan
c/o Incozen Therapeutics Pvt. Ltd.
"Spectrum" Discovery Zone
SP Biotech Park Phase I
Shameerpet Hyderabad 500 078 / IN
02 / VISWANADHA, Srikant
c/o Incozen Therapeutics Pvt. Ltd.
"Spectrum" Discovery Zone
SP Biotech Park Phase I
Shameerpet Hyderabad 500 078 / IN
03 / VARANASI, Kanthikiran, Vs.
c/o Incozen Therapeutics Pvt. Ltd.
"Spectrum" Discovery Zone
SP Biotech Park Phase I
Shameerpet Hyderabad 500 078 / IN
04 / MERIKAPUDI, Gayatri, Swaroop
c/o Incozen Therapeutics Pvt. Ltd.
"Spectrum" Discovery Zone
SP Biotech Park Phase I
Shameerpet Hyderabad 500 078 / IN
05 / VAKKALANKA, Swaroop, Kumar, V., S.
c/o Rhizen Pharmaceuticals SA
Fritz Courvoisier 40
CH-2300 La Chaux-de-Fonds / IN
 [2012/42]
Representative(s)Pons
Glorieta Rubén Darío 4
28010 Madrid / ES
[N/P]
Former [2018/15]Pons
Glorieta Ruben Dario 4
28010 Madrid / ES
Former [2012/42]Pons Ariño, Angel
Glorieta Ruben Dario 4
28010 Madrid / ES
Application number, filing date10776149.607.10.2010
[2018/15]
WO2010IB02539
Priority number, dateIN2009CHE243908.10.2009         Original published format: IN 2439CH2009
IN2009CHE263630.10.2009         Original published format: IN 2636CH2009
IN2010CHE15825.01.2010         Original published format: IN 158CH2010
IN2010CHE151302.06.2010         Original published format: IN 1513CH2010
IN2010CHE151402.06.2010         Original published format: IN 1514CH2010
IN2010CHE238519.08.2010         Original published format: IN 2385CH2010
US20090265540P01.12.2009         Original published format: US 265540 P
[2017/16]
Former [2012/42]IN2009CHE243908.10.2009
IN2009CHE263630.10.2009
IN2010CHE015825.01.2010
IN2010CHE151302.06.2010
IN2010CHE151402.06.2010
IN2010CHE238519.08.2010
US20090265540P01.12.2009
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2011042798
Date:14.04.2011
Language:EN
[2011/15]
Type: A1 Application with search report 
No.:EP2509974
Date:17.10.2012
Language:EN
The application published by WIPO in one of the EPO official languages on 14.04.2011 takes the place of the publication of the European patent application.
[2012/42]
Type: B1 Patent specification 
No.:EP2509974
Date:11.04.2018
Language:EN
[2018/15]
Search report(s)International search report - published on:EP14.04.2011
ClassificationIPC:C07D401/12, C07D403/12, C07D471/04, C07D487/04, A61P35/00, A61K31/4155
[2012/42]
CPC:
C07D473/34 (EP,CN,US); C07D403/12 (EP,CN,US); A61K31/4155 (EP,US);
A61K31/4184 (EP,US); A61K31/4192 (EP,US); A61K31/437 (EP,US);
A61K31/4709 (EP,US); A61K31/498 (EP,US); A61K31/52 (EP,US);
A61K31/522 (EP,US); A61K45/06 (US); A61P1/00 (EP);
A61P1/02 (EP); A61P1/04 (EP); A61P1/16 (EP);
A61P11/00 (EP); A61P11/02 (EP); A61P11/06 (EP);
A61P13/10 (EP); A61P13/12 (EP); A61P15/00 (EP);
A61P15/02 (EP); A61P17/00 (EP); A61P17/04 (EP);
A61P17/06 (EP); A61P19/02 (EP); A61P19/08 (EP);
A61P19/10 (EP); A61P21/00 (EP); A61P21/04 (EP);
A61P25/00 (EP); A61P25/14 (EP); A61P25/16 (EP);
A61P25/28 (EP); A61P27/02 (EP); A61P29/00 (EP);
A61P3/06 (EP); A61P3/10 (EP); A61P31/04 (EP);
A61P31/06 (EP); A61P31/08 (EP); A61P31/18 (EP);
A61P35/00 (EP); A61P35/02 (EP); A61P37/02 (EP);
A61P37/06 (EP); A61P37/08 (EP); A61P43/00 (EP);
A61P5/00 (EP); A61P5/14 (EP); A61P7/06 (EP);
A61P9/00 (EP); A61P9/10 (EP); A61P9/14 (EP);
C07D401/12 (EP,CN,US); C07D401/14 (EP,CN,US); C07D471/04 (EP,CN,US);
C07D473/08 (EP,CN,US); C07D487/04 (EP,US); Y02A50/30 (EP,US) (-)
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 [2012/42]
Extension statesBANot yet paid
MENot yet paid
TitleGerman:PYRAZOLDERIVATE ALS MODULATOREN DES CALCIUM-RELEASE-AKTIVIERTEN CALCIUMKANALS UND VERFAHREN ZUR BEHANDLUNG VON NICHT-KLEINZELLIGEM BRONCHIALKARZINOM[2012/42]
English:PYRAZOLES DERIVATIVES MODULATORS OF CALCIUM RELEASE-ACTIVATED CALCIUM CHANNEL AND METHODS FOR TREATMENT OF NON-SMALL CELL LUNG CANCER[2017/47]
French:DÉRIVÉS DE PYRAZOLE EN TANT QUE MODULATEURS DU CANAL CALCIQUE ACTIVÉ PAR LA LIBÉRATION DE CALCIUM ET MÉTHODE DE TRAITEMENT POUR LE CANCER DU POUMON À CELLULES NON PETITES[2012/42]
Former [2012/42]PYRAZOLES DERIVATIVES MODULATORS OF CALCIUM RELEASE -ACTIVATED CALCIUM CHANNEL AND METHODS FOR TREATMENT OF NON- SMALL CELL LUNG CANCER
Entry into regional phase07.05.2012National basic fee paid 
07.05.2012Designation fee(s) paid 
07.05.2012Examination fee paid 
Examination procedure07.05.2012Examination requested  [2012/42]
27.03.2013Amendment by applicant (claims and/or description)
25.09.2013Despatch of a communication from the examining division (Time limit: M04)
31.01.2014Reply to a communication from the examining division
06.11.2014Despatch of a communication from the examining division (Time limit: M06)
23.06.2015Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time
21.08.2015Reply to a communication from the examining division
21.01.2016Despatch of a communication from the examining division (Time limit: M04)
25.05.2016Reply to a communication from the examining division
07.10.2016Despatch of a communication from the examining division (Time limit: M04)
08.02.2017Reply to a communication from the examining division
23.05.2017Despatch of a communication from the examining division (Time limit: M04)
11.07.2017Reply to a communication from the examining division
31.10.2017Communication of intention to grant the patent
27.02.2018Fee for grant paid
27.02.2018Fee for publishing/printing paid
27.02.2018Receipt of the translation of the claim(s)
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  25.09.2013
Opposition(s)14.01.2019No opposition filed within time limit [2019/12]
Request for further processing for:The application is deemed to be withdrawn due to failure to reply to the examination report
21.08.2015Request for further processing filed
21.08.2015Full payment received (date of receipt of payment)
Request granted
14.09.2015Decision despatched
Fees paidRenewal fee
05.10.2012Renewal fee patent year 03
07.10.2013Renewal fee patent year 04
07.10.2014Renewal fee patent year 05
07.10.2015Renewal fee patent year 06
07.10.2016Renewal fee patent year 07
10.10.2017Renewal fee patent year 08
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Lapses during opposition  TooltipAL11.04.2018
[2018/46]
Cited inInternational search[IP]WO2010048559  (CALCIMEDICA INC [US], et al) [IP] 1-101 * paragraph [0002] * * claims 1,7 *;
 [Y]EP1875925  (ASTELLAS PHARMA INC [JP]) [Y] 1-101 * paragraph [0008] * * claim 4 *;
 [Y]WO2009076454  (CALCIMEDICA INC [US], et al) [Y] 1-101 * paragraphs [0002] , [ 0007] , [ and 0015]; claim 1 *
 [YD]  - YONETOKU Y ET AL, "Novel potent and selective Ca<2+> release-activated Ca<2+> (CRAC) channel inhibitors. Part 3: Synthesis and CRAC channel inhibitory activity of 4'-[(trifluoromethyl)pyrazol-1-yl]carboxanilides", BIOORGANIC & MEDICINAL CHEMISTRY, PERGAMON, GB, vol. 16, no. 21, doi:DOI:10.1016/J.BMC.2008.09.047, ISSN 0968-0896, (20081101), pages 9457 - 9466, (20080920), XP025545771 [YD] 1-101 * the whole document *

DOI:   http://dx.doi.org/10.1016/j.bmc.2008.09.047
 [Y]  - YONETOKU Y ET AL, "Novel potent and selective calcium-release-activated calcium (CRAC) channel inhibitors. Part 1: Synthesis and inhibitory activity of 5-(1-methyl-3-trifluoromethyl-1H-pyrazol-5-yl)-2-thiophenecarboxamides", BIOORGANIC & MEDICINAL CHEMISTRY, PERGAMON, GB, vol. 14, no. 14, doi:DOI:10.1016/J.BMC.2006.03.024, ISSN 0968-0896, (20060715), pages 4750 - 4760, (20060715), XP025133377 [Y] 1-101 * the whole document *

DOI:   http://dx.doi.org/10.1016/j.bmc.2006.03.024
 [I]  - YONETOKU Y ET AL, "Novel potent and selective calcium-release-activated calcium (CRAC) channel inhibitors. Part 2: Synthesis and inhibitory activity of aryl-3-trifluoromethylpyrazoles", BIOORGANIC & MEDICINAL CHEMISTRY, PERGAMON, GB, vol. 14, no. 15, doi:DOI:10.1016/J.BMC.2006.03.039, ISSN 0968-0896, (20060801), pages 5370 - 5383, (20060801), XP025133434 [I] 1-101 * the whole document *

DOI:   http://dx.doi.org/10.1016/j.bmc.2006.03.039
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