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Extract from the Register of European Patents

EP About this file: EP3256160

EP3256160 - STABLE LIQUID FORMULATION FOR MONOCLONAL ANTIBODIES [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  14.06.2019
Database last updated on 24.08.2024
FormerExamination is in progress
Status updated on  21.09.2018
FormerRequest for examination was made
Status updated on  17.11.2017
FormerThe international publication has been made
Status updated on  18.08.2017
Most recent event   Tooltip14.06.2019Application deemed to be withdrawnpublished on 17.07.2019  [2019/29]
Applicant(s)For all designated states
SANOFI
54, rue La Boétie
75008 Paris / FR
[2017/51]
Inventor(s)01 / BUSSEMER, Till
Sanofi-Aventis Deutschland GmbH
Patent Department
65926 Frankfurt / DE
02 / PIEPER, Annette
Sanofi-Aventis Deutschland GmbH
Patent Department
65926 Frankfurt / DE
03 / SAGI, Dijana
Sanofi-Aventis Deutschland GmbH
Patent Department
65926 Frankfurt / DE
04 / STREBE, Nina
Sanofi-Aventis Deutschland GmbH
Patent Department
65926 Frankfurt / DE
05 / YOUSSEFF, Ahmed
Sanofi-Aventis Deutschland GmbH
Patent Department
65926 Frankfurt / DE
 [2017/51]
Representative(s)Sanofi
Patent Department
46 avenue de la Grande Armée
75017 Paris / FR
[N/P]
Former [2017/51]Bouvet, Philippe, et al
Sanofi
Département Brevets
54, rue La Boétie
75008 Paris / FR
Application number, filing date16704440.312.02.2016
[2017/51]
WO2016EP53068
Priority number, dateEP2015030521813.02.2015         Original published format: EP 15305218
[2017/51]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2016128564
Date:18.08.2016
Language:EN
[2016/33]
Type: A1 Application with search report 
No.:EP3256160
Date:20.12.2017
Language:EN
The application published by WIPO in one of the EPO official languages on 18.08.2016 takes the place of the publication of the European patent application.
[2017/51]
Search report(s)International search report - published on:EP18.08.2016
ClassificationIPC:A61K39/395, C07K16/24
[2017/51]
CPC:
A61K39/39591 (EP,KR,US); A61K47/02 (US); A61K47/12 (US);
A61K47/183 (EP,US); A61K47/22 (US); A61K47/26 (EP,US);
A61K9/0019 (EP,US); A61K9/08 (EP,US); A61P1/04 (EP);
A61P17/06 (EP); A61P19/00 (EP); A61P19/02 (EP);
A61P29/00 (EP); C07K16/241 (EP,KR,US); C07K16/2866 (EP,KR,US);
C07K2317/94 (EP,KR,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 [2017/51]
TitleGerman:STABILE FLÜSSIGKEITSFORMULIERUNG FÜR MONOKLONALE ANTIKÖRPER[2017/51]
English:STABLE LIQUID FORMULATION FOR MONOCLONAL ANTIBODIES[2017/51]
French:FORMULATION LIQUIDE STABLE POUR DES ANTICORPS MONOCLONAUX[2017/51]
Entry into regional phase13.09.2017National basic fee paid 
13.09.2017Designation fee(s) paid 
13.09.2017Examination fee paid 
Examination procedure17.08.2017Date on which the examining division has become responsible
13.09.2017Examination requested  [2017/51]
21.03.2018Amendment by applicant (claims and/or description)
25.09.2018Despatch of a communication from the examining division (Time limit: M04)
06.02.2019Application deemed to be withdrawn, date of legal effect  [2019/29]
07.03.2019Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time  [2019/29]
Fees paidRenewal fee
14.02.2018Renewal fee patent year 03
Penalty fee
Additional fee for renewal fee
28.02.201904   M06   Not yet paid
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Cited inInternational search[XI]WO2014039903  (COHERUS BIOSCIENCES INC [US]) [X] 1-6,9-14,17,24-30 * page 17 - page 26 * [I] 7,8,15,16,18-23;
 [XI]WO2006044908  (GENENTECH INC [US], et al) [X] 1,2,4-6,9,10,26-30 * page 40 - page 42 * [I] 3,7,8,11-25;
 [XI]  - SAMPATHKUMAR KRISHNAN ET AL, Formulation and Process Development Strategies for Manufacturing Biopharmaceuticals; Chapter 16: DEVELOPMENT OF FORMULATIONS FOR THERAPEUTIC MONOCLONAL ANTIBODIES AND Fc FUSION PROTEINS, FORMULATION AND PROCESS DEVELOPMENT STRATEGIES FOR MANUFACTURING BIOPHARMACEUTICALS, JOHN WILEY & SONS, INC, HOBOKEN, N.J, PAGE(S) 383 - 427, (20100805), ISBN 978-0-470-11812-2, XP002712418 [X] 1-10,26-30 * table 16.1 * [I] 11-25

DOI:   http://dx.doi.org/10.1002/9780470595886.ch16
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.