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Extract from the Register of European Patents

EP About this file: EP3227686

EP3227686 - MULTIPLEXED IMMUNOHISTOCHEMISTRY ASSAYS FOR DIAGNOSIS AND TREATMENT OF CANCER [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  26.06.2020
Database last updated on 31.08.2024
FormerExamination is in progress
Status updated on  04.06.2019
FormerRequest for examination was made
Status updated on  08.09.2017
FormerThe international publication has been made
Status updated on  30.06.2017
Most recent event   Tooltip26.06.2020Application deemed to be withdrawnpublished on 29.07.2020  [2020/31]
Applicant(s)For all designated states
Ignyta, Inc.
11111 Flintkote Avenue
San Diego, CA 92121 / US
[2017/41]
Inventor(s)01 / CHRISTIANSEN, Jason, Hans
371D Pine Avenue
Carlsbad, CA 92008 / US
02 / MURPHY, Danielle, Anthea
752 Stevens Avenue
Solana Beach, CA 92075 / US
03 / BOOMER, Aaron, Scott
743 Sunset Drive
Vista, CA 92081 / US
04 / LAMOUREUX, Jennifer, Lyn
353 Aspen Creek Way
Oceanside, CA 92057 / US
 [2017/41]
Representative(s)HGF
HGF Limited
1 City Walk
Leeds LS11 9DX / GB
[N/P]
Former [2017/41]HGF Limited
4th Floor
Merchant Exchange
17-19 Whitworth Street West
Manchester M1 5WG / GB
Application number, filing date15864500.201.12.2015
[2017/41]
WO2015US63163
Priority number, dateUS201462086921P03.12.2014         Original published format: US 201462086921 P
[2017/41]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2016089853
Date:09.06.2016
Language:EN
[2016/23]
Type: A1 Application with search report 
No.:EP3227686
Date:11.10.2017
Language:EN
The application published by WIPO in one of the EPO official languages on 09.06.2016 takes the place of the publication of the European patent application.
[2017/41]
Search report(s)International search report - published on:US09.06.2016
(Supplementary) European search report - dispatched on:EP26.07.2018
ClassificationIPC:G01N33/574, A61P35/00, A61K31/496, C12Q1/6813, C12Q1/686, G01N27/447
[2018/35]
CPC:
G01N33/57484 (EP,US); A61K31/496 (EP,US); A61P35/00 (EP);
C12Q1/6813 (US); C12Q1/686 (US); G01N27/447 (US);
G01N33/57411 (US); G01N33/57415 (US); G01N33/57423 (US);
G01N33/57449 (US); G01N2800/52 (EP,US); G01N2800/7028 (US);
G01N33/57438 (EP,US) (-)
Former IPC [2017/41]G01N33/574, A61P35/00, A61K31/496
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 [2017/41]
TitleGerman:MULTIPLEXIERTE IMMUNHISTOCHEMIE-ASSAYS ZUR DIAGNOSE UND BEHANDLUNG VON KREBS[2017/41]
English:MULTIPLEXED IMMUNOHISTOCHEMISTRY ASSAYS FOR DIAGNOSIS AND TREATMENT OF CANCER[2017/41]
French:ANALYSES D'IMMUNOCYTOCHIMIE MULTIPLEXÉES POUR LE DIAGNOSTIC ET LE TRAITEMENT D'UN CANCER[2017/41]
Entry into regional phase29.06.2017National basic fee paid 
29.06.2017Search fee paid 
29.06.2017Designation fee(s) paid 
29.06.2017Examination fee paid 
Examination procedure29.06.2017Examination requested  [2017/41]
29.06.2017Date on which the examining division has become responsible
25.02.2019Amendment by applicant (claims and/or description)
07.06.2019Despatch of a communication from the examining division (Time limit: M06)
18.12.2019Application deemed to be withdrawn, date of legal effect  [2020/31]
24.01.2020Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time  [2020/31]
Fees paidRenewal fee
21.12.2017Renewal fee patent year 03
19.12.2018Renewal fee patent year 04
10.12.2019Renewal fee patent year 05
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Documents cited:Search[XY]WO2009013126  (NERVIANO MEDICAL SCIENCES SRL [IT], et al) [X] 1-3,5-14 * page 5 * * page 19, lines 1-2 * * page 85, line 15 - page 86, line 6 * * page 13, lines 19-20; compound 11 * * page 22, lines 5-7 * * pages 75,99 * [Y] 15;
 [XP]WO2015124697  (IGNYTA INC [US], et al) [XP] 1-3,5-15 * paragraphs [0036] , [0040] - [0043] * * page 41, paragraphs 248,249 *;
 [E]WO2016089760  (IGNYTA INC [US]) [E] 1-3,5-15 * paragraphs [0011] , [0014] - [0016] * * paragraphs [0063] - [0065] *;
 [Y]WO2012019132  (CELL SIGNALING TECHNOLOGY INC [US], et al) [Y] 15 * paragraphs [0009] , [0013] , [0022] , [0 27] *;
 [XP]WO2015157624  (SLOAN KETTERING INST CANCER [US]) [XP] 1,3,5,7-11,14 * page 2, lines 1-21 * * page 5, line 26 - page 6, line 18 * * page 7, line 21 - page 8, line 25 * * pages 7,32 *;
 [XI]  - Elena Ardini ET AL, "A highly potent, selective and orally available ALK inhibitor with demonstrated antitumor efficacy in ALK dependent lymphoma and non small cell lung cancer models | Cancer Research", Proc Am Assoc Cancer Res; 2009 Apr 18-22; Denver, CO. Philadelphia (PA): AACR; 2009, (20090418), page Abstract #3737, URL: http://cancerres.aacrjournals.org/content/69/9_Supplement/3737, (20180711), XP055491721 [X] 1,3,6,10-13,15 * abstract * [I] 5,7-9,14
 [XI]  - Ardini Ardini ET AL, "Characterization of NMS-E628, a small molecule inhibitor of anaplastic lymphoma kinase with antitumor efficacy in ALK-dependent lymphoma and non-small cell lung cancer models | Molecular Cancer Therapeutics", Mol Cancer Ther 2009;8(12 Suppl):A244., (20091115), page Abstract A243, URL: http://mct.aacrjournals.org/content/8/12_Supplement/A244, (20180711), XP055491735 [X] 1,3,6,10-13,15 * abstract * [I] 5,7-9,14
 [XI]  - Elena Ardini ET AL, "In vitro and in vivo activity of NMS-E628 against ALK mutations resistant to Xalkori. | Molecular Cancer Therapeutics", Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics: AACR; Mol Cancer Ther 2011;10(11 Suppl):Abstract nr A232, (20111112), page Abstract A232, URL: http://mct.aacrjournals.org/content/10/11_Supplement/A232, (20180711), XP055491739 [X] 1,3,10,11,14,15 * abstract * [I] 9
 [XI]  - Elena Ardini ET AL, "The ALK inhibitor NMS-E628 also potently inhibits ROS1 and induces tumor regression in ROS-driven models.", Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 2092, (20130406), page Abstract 2092, URL: http://cancerres.aacrjournals.org/content/73/8_Supplement/2092, (20180711), XP055491741 [X] 1,3,6,10-15 * abstract * [I] 5,7-9
 [XI]  - Filippo G De Braud ET AL, "Phase 1 open label, dose escalation study of RXDX101, an oral pan-trk, ROS1, and ALK inhibitor, in patients with advanced solid tumors with relevant molecular alterations.: Journal of Clinical Oncology: Vol 32, No 15_suppl", ournal of Clinical Oncology 32, no. 15_suppl (May 20 2014) 2502-2502, (20140520), URL: http://ascopubs.org/doi/abs/10.1200/jco.2014.32.15_suppl.2502, (20180711), XP055491745 [X] 1,3,6,14,15 * abstract * [I] 5,7-13
 [XI]  - ARDINI E ET AL, "NMS-E628, a potent and orally available small molecule inhibitor of anaplastic lymphoma kinase, reduces tumor growth in an intracranial model of ALK-dependent NSCLC", EUROPEAN JOURNAL OF CANCER. SUPPLEMENT, PERGAMON, OXFORD, GB, vol. 8, no. 7, doi:10.1016/S1359-6349(10)71875-9, ISSN 1359-6349, (20101101), page 59, (20101101), XP027497858 [X] 1,3,6,14,15 * abstract * [I] 5,7-13

DOI:   http://dx.doi.org/10.1016/S1359-6349(10)71875-9
 [XI]  - David Anderson ET AL, "Inhibition of Trk-driven tumors by the pan-Trk inhibitor RXDX-10", EORTC-NCI-AACR 2014, (20141101), page abstract 310, URL: https://ignyta.com/wp-content/uploads/2016/10/Anderson-et-al_EORTC-2014.pdf.pdf, (20180711), XP055491752 [X] 1,3,5-7,10-15 * abstract * [I] 8,9
International search[Y]WO2014046730  (VENTANA MED SYST INC [US]) [Y] 1-32 * ; page 2, lines 1-20; page 5, lines 1-10; page 8, lines 1-6; page 11, lines,15-35; page 12, lines 1-15; page 18, lines 29-33; page 19, lines 1-35 *;
 [Y]WO2013174876  (NERVIANO MEDICAL SCIENCES SRL [IT]) [Y] 1-32 * ; page 1 paragraph 1, page 2 paragraph 3 *;
 [Y]US2013303461  (IAFRATE ANTHONY JOHN [US], et al) [Y] 6, 23/6 * ; paragraphs [0017]-[0019] *
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.