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Extract from the Register of European Patents

EP About this file: EP3469083

EP3469083 - COMPLEMENT COMPONENT C5 iRNA COMPOSITIONS AND METHODS OF USE THEREOF FOR TREATING PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (PNH) [Right-click to bookmark this link]
StatusExamination is in progress
Status updated on  31.07.2020
Database last updated on 14.06.2024
FormerRequest for examination was made
Status updated on  15.03.2019
FormerThe international publication has been made
Status updated on  16.12.2017
Formerunknown
Status updated on  13.07.2017
Most recent event   Tooltip05.01.2024Change - applicantpublished on 07.02.2024  [2024/06]
Applicant(s)For all designated states
Alnylam Pharmaceuticals, Inc.
675 West Kendall Street
Henri A. Termeer Square
Cambridge, MA 02142 / US
[2024/06]
Former [2019/16]For all designated states
Alnylam Pharmaceuticals, Inc.
300 Third Street, 3rd Floor
Cambridge, MA 02142 / US
Inventor(s)01 / NAJAFIAN, Nader
300 Third Street 3rd Floor
Cambridge MA 02142 / US
02 / KIM, Jae
300 Third Street 3rd Floor
Cambridge MA 02142 / US
03 / VAROGLU, Mustafa
300 Third Street 3rd Floor
Cambridge MA 02142 / US
04 / ROBBIE, Gabriel
300 Third Street 3rd Floor
Cambridge MA 02142 / US
 [2019/16]
Representative(s)Hoffmann Eitle
Patent- und Rechtsanwälte PartmbB
Arabellastraße 30
81925 München / DE
[2019/16]
Application number, filing date17734891.909.06.2017
[2019/16]
WO2017US36775
Priority number, dateUS201662348564P10.06.2016         Original published format: US 201662348564 P
US201662429448P02.12.2016         Original published format: US 201662429448 P
[2019/16]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2017214518
Date:14.12.2017
Language:EN
[2017/50]
Type: A1 Application with search report 
No.:EP3469083
Date:17.04.2019
Language:EN
The application published by WIPO in one of the EPO official languages on 14.12.2017 takes the place of the publication of the European patent application.
[2019/16]
Search report(s)International search report - published on:EP14.12.2017
ClassificationIPC:C12N15/113, A61K31/713, A61K39/395, C07H21/00
[2019/16]
CPC:
C12N15/113 (EP,US); A61K39/3955 (US); A61P13/02 (EP,US);
A61P43/00 (EP); C07K16/18 (US); A61K2039/545 (US);
C12N2310/14 (EP,US); C12N2310/315 (EP,US); C12N2310/321 (US);
C12N2310/322 (US); C12N2310/346 (EP,US); C12N2310/351 (EP,US);
C12N2320/31 (EP,US); C12N2320/35 (EP,US) (-)
C-Set:
C12N2310/321, C12N2310/3521 (EP,US);
C12N2310/322, C12N2310/3533 (US,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 [2019/16]
TitleGerman:GEGEN KOMPLEMENTKOMPONENTE C5 GERICHTETE IRNA-ZUSAMMENSETZUNGEN UND VERFAHREN ZUR VERWENDUNG DAVON ZUR BEHANDLUNG VON PAROXYSMALER NÄCHTLICHER HÄMOGLOBINURIE (PNH)[2019/16]
English:COMPLEMENT COMPONENT C5 iRNA COMPOSITIONS AND METHODS OF USE THEREOF FOR TREATING PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (PNH)[2019/16]
French:COMPOSITIONS D'ARNI DU COMPOSANT C5 DU COMPLÉMENT ET LEURS MÉTHODES D'UTILISATION POUR TRAITER L'HÉMOGLOBINURIE PAROXYSTIQUE NOCTURNE (HPN)[2019/16]
Entry into regional phase09.01.2019National basic fee paid 
09.01.2019Designation fee(s) paid 
09.01.2019Examination fee paid 
Examination procedure09.01.2019Amendment by applicant (claims and/or description)
09.01.2019Examination requested  [2019/16]
09.01.2019Date on which the examining division has become responsible
04.08.2020Despatch of a communication from the examining division (Time limit: M08)
10.05.2021Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time
16.07.2021Reply to a communication from the examining division
Request for further processing for:The application is deemed to be withdrawn due to failure to reply to the examination report
16.07.2021Request for further processing filed
16.07.2021Full payment received (date of receipt of payment)
Request granted
26.07.2021Decision despatched
Fees paidRenewal fee
27.06.2019Renewal fee patent year 03
29.06.2020Renewal fee patent year 04
28.06.2021Renewal fee patent year 05
27.06.2022Renewal fee patent year 06
27.06.2023Renewal fee patent year 07
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Cited inInternational search[AD]WO2009073809  (ALNYLAM PHARMACEUTICALS INC [US], et al) [AD] 42-46 * the whole document *;
 [I]WO2014160129  (ALNYLAM PHARMACEUTICALS INC [US]) [I] 1-49 * the whole document *;
 [I]WO2016040589  (ALNYLAM PHARMACEUTICALS INC [US]) [I] 1-49 * the whole document *;
 [I]WO2016044419  (ALNYLAM PHARMACEUTICALS INC [US]) [I] 1-49 * the whole document *;
 [XP]WO2016201301  (ALNYLAM PHARMACEUTICALS INC [US]) [XP] 1-49* the whole document *;
 [A]  - A. Hill ET AL, "ALN-CC5 PHASE 1 STUDY DESIGN Objectives Complement Assay Benchmarks from Select Published Literature ALN-CC5 PHASE 1 PRELIMINARY STUDY RESULTS* Demographics and Baseline Characteristics Safety and Tolerability* Part A: Single Ascending Dose (SAD) Part B: Multiple Ascending Dose (MAD)", (20151201), URL: https://s3.amazonaws.com/academia.edu.documents/44825766/ASH-2015_CC5_Hill_Poster_010615.pdf?AWSAccessKeyId=AKIAIWOWYYGZ2Y53UL3A&Expires=1503481629&Signature=behBRCmPpcO3Nbv7%2BZE0UHvjWIk%3D&response-content-disposition=inline%3B%20filename%3DA_Subcutaneously_Administered_Investigat.pdf, (20170823), XP055400561 [A] 1-49 * the whole document *
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