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Extract from the Register of European Patents

EP About this file: EP3329896

EP3329896 - TWO PART FORMULATION SYSTEM FOR OPHTHALMIC DELIVERY [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  10.03.2023
Database last updated on 06.11.2024
FormerExamination is in progress
Status updated on  07.04.2020
FormerRequest for examination was made
Status updated on  19.10.2018
FormerThe application has been published
Status updated on  04.05.2018
Most recent event   Tooltip10.03.2023Application deemed to be withdrawnpublished on 12.04.2023  [2023/15]
Applicant(s)For all designated states
Allergan, Inc.
2525 Dupont Drive
Irvine, CA 92612 / US
[2018/23]
Inventor(s)01 / Gore, Anuradha V.
8 Del Rey
Irvine, CA California 92612 / US
02 / Shankar, Sai
2404 Spectrum
Irvine, CA California 92618 / US
03 / Likitlersuang, Sukhon
611 Wycliffe
Irvine, CA California 92602 / US
04 / Pujara, Chetan P.
6 Wheeler
Irvine, CA California 92620 / US
05 / Neervannan, Sesha
32 Trailing Ivy
Irvine, CA California 92656 / US
 [2018/23]
Representative(s)Hoffmann Eitle
Patent- und Rechtsanwälte PartmbB
Arabellastraße 30
81925 München / DE
[2018/23]
Application number, filing date18151604.826.07.2012
[2018/23]
Priority number, dateUS201161511753P26.07.2011         Original published format: US 201161511753 P
[2018/23]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report 
No.:EP3329896
Date:06.06.2018
Language:EN
[2018/23]
Search report(s)(Supplementary) European search report - dispatched on:EP12.04.2018
ClassificationIPC:A61J1/00, A61K9/00, B65D81/32, A61K47/34, A61K38/13, A61K9/08, A61K31/568, A61K31/417, A61K31/559, A61K31/4025
[2018/23]
CPC:
A61K38/13 (EP,US); A61K31/4025 (EP,US); A61K31/417 (EP,US);
A61K31/559 (EP,US); A61K31/568 (EP,US); A61K47/02 (US);
A61K47/12 (US); A61K47/18 (US); A61K47/26 (US);
A61K47/34 (EP,US); A61K47/40 (US); A61K9/0048 (EP,US);
A61K9/08 (EP,US); A61P27/02 (EP) (-)
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 [2018/47]
Former [2018/23]AL,  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 
TitleGerman:SYSTEM MIT EINER ZWEITEILIGEN FORMULIERUNG ZUR OPHTHALMISCHEN VERABREICHUNG[2018/23]
English:TWO PART FORMULATION SYSTEM FOR OPHTHALMIC DELIVERY[2018/23]
French:SYSTÈME DE FORMULATION EN DEUX PARTIES POUR ADMINISTRATION OPHTALMIQUE[2018/23]
Examination procedure14.08.2018Amendment by applicant (claims and/or description)
16.10.2018Examination requested  [2018/47]
16.10.2018Date on which the examining division has become responsible
14.04.2020Despatch of a communication from the examining division (Time limit: M06)
26.10.2020Reply to a communication from the examining division
03.05.2022Despatch of a communication from the examining division (Time limit: M06)
15.11.2022Application deemed to be withdrawn, date of legal effect  [2023/15]
06.12.2022Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time  [2023/15]
Parent application(s)   TooltipEP12762425.2  / EP2736475
Fees paidRenewal fee
15.01.2018Renewal fee patent year 03
15.01.2018Renewal fee patent year 04
15.01.2018Renewal fee patent year 05
15.01.2018Renewal fee patent year 06
27.07.2018Renewal fee patent year 07
29.07.2019Renewal fee patent year 08
27.07.2020Renewal fee patent year 09
27.07.2021Renewal fee patent year 10
11.07.2022Renewal fee patent year 11
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Documents cited:Search[I]JPH0558906  (SANKYO CO);
 [A]US5409904  (HECHT GERALD [US], et al);
 [A]WO2009046967  (FOVEA PHARMACEUTICALS SA [FR], et al);
 [I]WO2009088570  (SIRION THERAPEUTICS INC [US], et al);
ExaminationUS2009221984
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.