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Extract from the Register of European Patents

EP About this file: EP1824498

EP1824498 - METHODS AND COMPOSITIONS FOR TREATING CELLULAR PROLIFERATIVE DISEASES [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  20.08.2010
Database last updated on 04.12.2024
Most recent event   Tooltip20.08.2010Application deemed to be withdrawnpublished on 22.09.2010  [2010/38]
Applicant(s)For all designated states
Massachusetts Institute of Technology
77 Massachusetts Avenue
Cambridge, MA 02139 / US
[N/P]
Former [2007/35]For all designated states
THE MASSACHUSETTS INSTITUTE OF TECHNOLOGY
77 Massachusetts Avenue
Cambridge, MA 02139 / US
Inventor(s)01 / YAFFE, Michael, B.
1 Chesbrough Road
West Roxbury, MA 02132 / US
02 / MANKE, Isaac, A.
500 Memorial Drive, 355
Cambridge, MA 02139 / US
03 / REINHARDT, Hans, Christian
34 Essex Street
Cambride, MA 02139 / US
04 / LIM, Daniel
520 Cambridge Street, Suite 2
Cambridge, MA 02141 / US
 [2007/35]
Representative(s)Lahrtz, Fritz
Patentanwälte
Isenbruck Bösl Hörschler PartG mbB
Prinzregentenstraße 68
81675 München / DE
[N/P]
Former [2007/35]Lahrtz, Fritz
Isenbruck Bösl Hörschler Wichmann Huhn, Patentattorneys, Prinzregentenstrasse 68
81675 München / DE
Application number, filing date05851642.814.11.2005
[2007/35]
WO2005US41294
Priority number, dateUS20040627352P12.11.2004         Original published format: US 627352 P
[2007/35]
Filing languageEN
Procedural languageEN
PublicationType: A2 Application without search report
No.:WO2006053315
Date:18.05.2006
Language:EN
[2006/20]
Type: A2 Application without search report 
No.:EP1824498
Date:29.08.2007
Language:EN
The application published by WIPO in one of the EPO official languages on 18.05.2006 takes the place of the publication of the European patent application.
[2007/35]
Search report(s)International search report - published on:US09.11.2006
(Supplementary) European search report - dispatched on:EP27.05.2009
ClassificationIPC:A61K31/00, A61K31/713, A61K38/08, A61N5/00, C12N15/11, A61K45/06, A61K47/48, C12Q1/48, C07K7/06, A61P35/00
[2009/24]
CPC:
C07K7/08 (EP,US); A61K31/00 (EP,US); A61K31/522 (EP,US);
A61K31/7048 (EP,US); A61K31/7072 (EP,US); A61K31/713 (EP,US);
A61K41/00 (EP,US); A61K45/06 (EP,US); A61K47/645 (EP,US);
A61K47/6455 (EP,US); A61P35/00 (EP); A61P35/02 (EP);
A61P43/00 (EP); C07K7/06 (EP,US); C12N15/1137 (EP,US);
C12N9/1205 (EP,US); C12Q1/485 (EP,US); C12Y207/11001 (EP,US);
G01N33/573 (EP,US); G01N33/57407 (EP,US); A61K38/00 (EP,US);
C07K2299/00 (EP,US); C12N2310/14 (EP,US); G01N1/30 (EP,US);
G01N2333/9121 (EP,US); G01N2500/00 (EP,US); G01N2500/02 (EP,US) (-)
C-Set:
A61K31/00, A61K2300/00 (EP,US);
A61K41/00, A61K2300/00 (US,EP)
Former IPC [2007/35]A61K31/7088
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 [2007/35]
Extension statesALNot yet paid
BANot yet paid
HRNot yet paid
MKNot yet paid
YUNot yet paid
TitleGerman:VERFAHREN UND ZUSAMMENSETZUNGEN ZUR BEHANDLUNG PROLIFERATIVER ZELLKRANKHEITEN[2007/35]
English:METHODS AND COMPOSITIONS FOR TREATING CELLULAR PROLIFERATIVE DISEASES[2007/35]
French:METHODES ET COMPOSITIONS DE TRAITEMENT DE MALADIES PROLIFERATIVES CELLULAIRES[2007/35]
Entry into regional phase12.06.2007National basic fee paid 
12.06.2007Search fee paid 
12.06.2007Designation fee(s) paid 
12.06.2007Examination fee paid 
Examination procedure12.06.2007Amendment by applicant (claims and/or description)
12.06.2007Examination requested  [2007/35]
16.09.2009Despatch of a communication from the examining division (Time limit: M06)
27.03.2010Application deemed to be withdrawn, date of legal effect  [2010/38]
03.05.2010Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time  [2010/38]
Fees paidRenewal fee
27.11.2007Renewal fee patent year 03
25.11.2008Renewal fee patent year 04
25.11.2009Renewal fee patent year 05
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Documents cited:Search[A]US2004209897  (VERNIER WILLIAM F [US], et al) [A] 1,2,6,11 * column W *;
 [PA]  - MANKE ISAAC A ET AL, "MAPKAP kinase-2 is a cell cycle checkpoint kinase that regulates the G2/M transition and S phase progression in response to UV irradiation", MOLECULAR CELL, (20050107), vol. 17, no. 1, ISSN 1097-2765, pages 37 - 48, XP002525960 [PA] 1,2,6,11 * the whole document *

DOI:   https://dx.doi.org/10.1016/J.MOLCEL.2004.11.021
 [A]  - HIROSE YUICHI ET AL, "The p38 mitogen-activated protein kinase pathway links the DNA mismatch repair system to the G2 checkpoint and to resistance to chemotherapeutic DNA-methylating agents.", MOLECULAR AND CELLULAR BIOLOGY, (200311), vol. 23, no. 22, ISSN 0270-7306, pages 8306 - 8315, XP002525961 [A] 1,2,6,11 * the whole document *

DOI:   https://dx.doi.org/10.1128/MCB.23.22.8306-8315.2003
 [PA]  - KUROSU T ET AL, "p38 MAP kinase plays a role in G2 checkpoint activation and inhibits apoptosis of human B cell lymphoma cells treated with etoposide", APOPTOSIS ; AN INTERNATIONAL JOURNAL ON PROGRAMMED CELL DEATH, KLUWER ACADEMIC PUBLISHERS, BO, (20051001), vol. 10, no. 5, ISSN 1573-675X, pages 1111 - 1120, XP019204740 [PA] 1,2,6,11 * the whole document *

DOI:   https://dx.doi.org/10.1007/s10495-005-3372-z
 [A]  - HAN Q ET AL, "Rac1-MKK3-p38-MAPKAPK2 pathway promotes urokinase plasminogen activator mRNA stability in invasive breast cancer cells", JOURNAL OF BIOLOGICAL CHEMISTRY 20021213 AMERICAN SOCIETY FOR BIOCHEMISTRY AND MOLECULAR BIOLOGY INC. US, (20021213), vol. 277, no. 50, pages 48379 - 48385, XP002525962 [A] 1,2,6,11 * the whole document *

DOI:   https://dx.doi.org/10.1074/JBC.M.2095542200
 [T]  - REINHARDT H CHRISTIAN ET AL, "p53-deficient cells rely on ATM- and ATR-mediated checkpoint signaling through the p38MAPK/MK2 pathway for survival after DNA damage", CANCER CELL, (200702), vol. 11, no. 2, ISSN 1535-6108, pages 175 - 189, XP002525963 [T] 1,2,6,11 * the whole document *

DOI:   https://dx.doi.org/10.1016/J,CCR.2006.11.024
 [A]  - SHAO RONG-GUANG ET AL, "Abrogation of Chk1-mediated S/G2 checkpoint by UCN-01 enhances ara-C-induced cytotoxicity in human colon cancer cells", ACTA PHARMACOLOGICA SINICA, (200406), vol. 25, no. 6, ISSN 1671-4083, pages 756 - 762, XP002525964 [A] 1,2,6,11 * the whole document *
 [A]  - TSE ARCHIE N ET AL, "Potentiation of cytotoxicity of topoisomerase I poison by concurrent and sequential treatment with the checkpoint inhibitor UCN-01 involves disparate mechanisms resulting in either p53-independent clonogenic suppression or p53-dependent mitotic catastrophe", CANCER RESEARCH, (20040915), vol. 64, no. 18, ISSN 0008-5472, pages 6635 - 6644, XP002525965 [A] 1,2,6,11 * the whole document *

DOI:   https://dx.doi.org/10.1158/0008-5472.CAN-04-0841
International search[Y]US6683172  (KOTLYAROV ALEXEY [DE], et al);
 [Y]WO2004055019  (PHARMACIA CORP [US], et al);
 [Y]  - SPORTSMAN J.R. ET AL., "Fluorescence Polarization Assays in Signal Transduction Discovery", COMB. CHEM. HIGH THROUGHPUT SCREENING, (2003), vol. 6, pages 195 - 200, XP009061455
 [Y]  - HAYEES K. ET AL., "Effect of Protein Kinase Inhibitors on Activity of Mammalian Small Heat-Shock Protein (HSP25) Kinase", BIOCHEM. PHARM., (1997), vol. 53, pages 1239 - 1247, XP008119459

DOI:   https://dx.doi.org/10.1016/S0006-2952(96)00877-5
 [A]  - CHENG J.C. ET AL., "RNA interference and human disease", MOL. GEN. METAB., (2003), vol. 80, pages 121 - 128, XP001157375

DOI:   https://dx.doi.org/10.1016/j.ymgme.2003.08.011
 [Y]  - HAN Q. ET AL., "RAc1-MKK3-p38/MAPKAPK2 Pathway Promotes Urokinase Plasminogen Activator mRNA Stability in Invasive Breast Cancer Cells", J. BIO. CHEM., (2002), vol. 277, no. 50, pages 48379 - 48385, XP002525962

DOI:   https://dx.doi.org/10.1074/JBC.M.2095542200
 [Y]  - HIROSE Y. ET AL., "Cooperative function of Chk1 and p38 pathways in activating G2 arrest following exposure to temozolomide", J. NEUROSURG., (2004), vol. 100, pages 1060 - 1065, XP009115843

DOI:   https://dx.doi.org/10.3171/jns.2004.100.6.1060
 [Y]  - MIKHAILOV A. ET AL., "Topoisomerase II and histone deacetylase inhibitors delay the G2/M transition by triggering the p38 MAPK checkpoint pathway", J. CELL BIO., (2004), vol. 166, no. 4, pages 517 - 526, XP008119460

DOI:   https://dx.doi.org/10.1083/jcb.200405167
 [A]  - CARRASSA L. ET AL., "Chk1, but not Chk2, is Involved in the Cellular Response to DNA Damaging Agents", CELL CYCLE, (2004), vol. 3, no. 9, pages 1177 - 1181, XP009115840
 [Y]  - IGNATOVICH I.A. ET AL., "Complexes of Plasmid DNA with Basic Domain 47-57 of the HIV-1 Tat Protein Are Transferred to Mammalian Cells by Endocytosis-mediated Pathways", J. BIO. CHEM., (2003), vol. 278, no. 43, pages 42625 - 42636, XP002297599

DOI:   https://dx.doi.org/10.1074/jbc.M301431200
 [Y]  - SAALIK P. ET AL, "Protein Cargo Delivery Properties of Cell-Penetrating Peptides: A Comparative Study", BIOCONJ. CHEM., (2004), vol. 15, pages 1246 - 1253, XP008119461

DOI:   https://dx.doi.org/10.1021/bc049938y
 [A]  - SAKLATVALA J., "The p38 MAP kinase pathway as a therapeutic target in inflammatory disease", CURR. OP. PHARM., (2004), vol. 4, pages 373 - 377, XP008119482

DOI:   https://dx.doi.org/10.1016/j.coph.2004.03.009
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.