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Extract from the Register of European Patents

EP About this file: EP3236948

EP3236948 - COMBINATION OF RAF INHIBITORS AND AURORA KINASE INHIBITORS [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  27.11.2020
Database last updated on 03.09.2024
FormerGrant of patent is intended
Status updated on  01.03.2020
FormerRequest for examination was made
Status updated on  29.09.2017
FormerThe international publication has been made
Status updated on  19.07.2017
Most recent event   Tooltip27.11.2020Application deemed to be withdrawnpublished on 30.12.2020  [2020/53]
Applicant(s)For all designated states
DOT Therapeutics-1, Inc.
2765 Sand Hill Road
Menlo Park, CA 94025 / US
[2020/18]
Former [2017/44]For all designated states
Millennium Pharmaceuticals, Inc.
40 Landsdowne Street
Cambridge, MA 02139 / US
Inventor(s)01 / BOZON, Viviana
99 Pickwick Road
West Newton, MA 02465 / US
02 / GALVIN, Katherine, M.
52 Greenlawn Avenue
Newton, MA 02459 / US
 [2017/44]
Representative(s)Harris, Jennifer Lucy
Kilburn & Strode LLP
Lacon London
84 Theobalds Road
London WC1X 8NL / GB
[2017/44]
Application number, filing date15874329.422.12.2015
[2017/44]
WO2015US67459
Priority number, dateUS201462096020P23.12.2014         Original published format: US 201462096020 P
[2017/44]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2016106357
Date:30.06.2016
Language:EN
[2016/26]
Type: A1 Application with search report 
No.:EP3236948
Date:01.11.2017
Language:EN
The application published by WIPO in one of the EPO official languages on 30.06.2016 takes the place of the publication of the European patent application.
[2017/44]
Search report(s)International search report - published on:US30.06.2016
(Supplementary) European search report - dispatched on:EP31.08.2018
ClassificationIPC:A61K31/506, A61K31/55, A61K45/06, A61P35/00, A61K9/14
[2018/39]
CPC:
A61K31/506 (EP,US); A61K31/55 (EP,US); A61K45/06 (EP,US);
A61P35/00 (EP,US); A61K2300/00 (US)
C-Set:
A61K31/506, A61K2300/00 (US,EP);
A61K31/55, A61K2300/00 (EP,US)
Former IPC [2017/44]A61K9/14
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 [2017/44]
TitleGerman:KOMBINATION AUS RAF-INHIBITOREN UND AURORAKINASE-INHIBITOREN[2017/44]
English:COMBINATION OF RAF INHIBITORS AND AURORA KINASE INHIBITORS[2017/44]
French:COMBINAISON D'INHIBITEURS DE RAF ET D'INHIBITEURS DE KINASES AURORA[2017/44]
Entry into regional phase19.07.2017National basic fee paid 
19.07.2017Search fee paid 
19.07.2017Designation fee(s) paid 
19.07.2017Examination fee paid 
Examination procedure19.07.2017Examination requested  [2017/44]
19.07.2017Date on which the examining division has become responsible
26.03.2019Amendment by applicant (claims and/or description)
02.03.2020Communication of intention to grant the patent
14.07.2020Application deemed to be withdrawn, date of legal effect  [2020/53]
14.08.2020Despatch of communication that the application is deemed to be withdrawn, reason: fee for grant / fee for printing not paid in time  [2020/53]
Fees paidRenewal fee
27.12.2017Renewal fee patent year 03
31.12.2018Renewal fee patent year 04
27.12.2019Renewal fee patent year 05
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Documents cited:Search[A]WO2013144923  (TAKEDA PHARMACEUTICAL [JP]) [A] 1-15 * abstract * * page 4, paragraph 19; claim - *;
 [Y]US2013303519  (ECSEDY JEFFREY A [US], et al) [Y] 1-7,9-12 * abstract *;
 [E]WO2015193212  (WORLDWIDE INNOVATIVE NETWORK [FR]) [E] 1-8 * page 5, line 21 - line 23 * * page 6, line 8 - line 9 * * tables 1,6,7 * * claim 15 *;
 [Y]  - MIDDLETON M ET AL, "First-in-human phase 1 study of MLN2480, an investigational oral pan-RAF kinase inhibitor, in patients (pts) with relapsed or refractory solid tumors, including BRAF/NRAS-mutant melanoma", EUROPEAN JOURNAL OF CANCER, & 26TH EORTC-NCI-AACR SYMPOSIUM ON MOLECULAR TARGETS AND CANCER THERAPEUTICS; BARCELONA, SPAIN; NOVEMBER 18 -21, 2014, (201411), vol. 50, no. Suppl. 6, ISSN 0959-8049, page 117, XP002784040 [Y] 1-7,9-12 * the whole document *

DOI:   http://dx.doi.org/10.1016/S0959-8049(14)70490-3
 [XP]  - "A Phase 1B Study of MLN2480 in Combination With MLN0128 or Alisertib, or Paclitaxel, or Cetuximab, or Irinotecan in Adult Participants With Advanced Nonhematologic Malignancies", (20141230), ClinicalTrials.gov, URL: https://clinicaltrials.gov/ct2/show/NCT02327169, (20180820), XP002784013 [XP] 1-15 * the whole document *
International search[Y]US2006128624  (CHEUNG WING [US], et al) [Y] 38* entire document *;
 [Y]US2009036419  (CHEN WEIRONG [US], et al) [Y] 29-31, 38 * entire document *;
 [Y]US2013245039  (HIGGINS BRIAN [US], et al) [Y] 31 * entire document *;
 [Y]US2013303519  (ECSEDY JEFFREY A [US], et al) [Y] 29-31, 38 * entire document *;
 [Y]WO2014018725  (NOVARTIS AG [CH], et al) [Y] 30, 38 * entire document *;
 [X]US2014194442  (SOLCA FLAVIO [AT], et al) [X] 1-7, 20 * entire document *
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.