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Extract from the Register of European Patents

EP About this file: EP1064277

EP1064277 - 2-(2,6-DIOXOPIPERIDIN-3-YL)ISOINDOLINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF INFLAMMATORY CYTOKINES [Right-click to bookmark this link]
StatusNo opposition filed within time limit
Status updated on  12.05.2006
Database last updated on 25.12.2024
Most recent event   Tooltip12.05.2006No opposition filed within time limitpublished on 14.06.2006  [2006/24]
Applicant(s)For all designated states
CELGENE CORPORATION
7 Powder Horn Drive
Warren, NJ 07059 / US
[N/P]
Former [2001/06]For all designated states
CELGENE CORPORATION
7 Powder Horn Drive
Warren New Jersey 07059 / US
Former [2001/01]For all designated states
Gelgene Corporation
7 Powder Horn Drive
Warren, NJ 07059 / US
Inventor(s)01 / MAN, Hon-wah
102 Bermuda Drive
Neshanic Station, NJ 08853 / US
02 / MULLER, George, W.
250 Windmill Court
Bridgewater, NJ 08807 / US
[2001/01]
Representative(s)Lawrence, John, et al
Barker Brettell LLP
100 Hagley Road
Edgbaston
Birmingham B16 8QQ / GB
[N/P]
Former [2001/01]Lawrence, John, et al
Barker Brettell 138 Hagley Road Edgbaston
Birmingham B16 9PW / GB
Application number, filing date99911393.916.03.1999
[2001/01]
WO1999US05562
Priority number, dateUS19980078180P16.03.1998         Original published format: US 78180 P
[2001/01]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO9947512
Date:23.09.1999
Language:EN
[1999/38]
Type: A1 Application with search report 
No.:EP1064277
Date:03.01.2001
Language:EN
The application published by WIPO in one of the EPO official languages on 23.09.1999 takes the place of the publication of the European patent application.
[2001/01]
Type: B1 Patent specification 
No.:EP1064277
Date:15.06.2005
Language:EN
[2005/24]
Search report(s)International search report - published on:EP23.09.1999
ClassificationIPC:C07D401/04, A61K31/445
[2001/01]
CPC:
C07D401/04 (EP,KR,US); A61K31/454 (EP,KR,US); A61P1/00 (EP);
A61P1/04 (EP); A61P11/00 (EP); A61P11/06 (EP);
A61P19/02 (EP); A61P29/00 (EP); A61P31/00 (EP);
A61P31/18 (EP); A61P35/00 (EP); A61P37/00 (EP);
A61P37/02 (EP); A61P37/04 (EP); A61P37/06 (EP);
A61P43/00 (EP); Y02A50/30 (EP,US) (-)
Designated contracting statesAT,   BE,   CH,   CY,   DE,   DK,   ES,   FI,   FR,   GB,   GR,   IE,   IT,   LI,   LU,   MC,   NL,   PT,   SE [2001/01]
Extension statesAL07.10.2000
LT07.10.2000
LV07.10.2000
MK07.10.2000
RO07.10.2000
SI07.10.2000
TitleGerman:2-(2,6-DIOXOPIPERIDIN-3-YL)ISOINDOLIN DERIVATE, DEREN HERSTELLUNG UND DEREN VERWENDUNG ALS INHIBITOREN VON ENTZÜNDUNGSZYTOKINEN[2001/01]
English:2-(2,6-DIOXOPIPERIDIN-3-YL)ISOINDOLINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF INFLAMMATORY CYTOKINES[2001/01]
French:DERIVES DE 2-(2,6-DIOXOPIPERIDIN-3-YL)ISO-INDOLINE, LEUR PREPARATION ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE CYTOKINES INFLAMMATOIRES[2001/01]
Entry into regional phase07.10.2000National basic fee paid 
07.10.2000Designation fee(s) paid 
07.10.2000Examination fee paid 
Examination procedure13.10.1999Request for preliminary examination filed
International Preliminary Examining Authority: US
07.10.2000Examination requested  [2001/01]
11.04.2002Despatch of a communication from the examining division (Time limit: M04)
25.07.2002Reply to a communication from the examining division
18.10.2002Despatch of a communication from the examining division (Time limit: M06)
24.04.2003Reply to a communication from the examining division
18.12.2003Despatch of a communication from the examining division (Time limit: M04)
23.04.2004Reply to a communication from the examining division
14.12.2004Communication of intention to grant the patent
14.04.2005Fee for grant paid
14.04.2005Fee for publishing/printing paid
Divisional application(s)EP03012168.5  / EP1357120
Opposition(s)16.03.2006No opposition filed within time limit [2006/24]
Fees paidRenewal fee
05.03.2001Renewal fee patent year 03
04.03.2002Renewal fee patent year 04
05.03.2003Renewal fee patent year 05
29.03.2004Renewal fee patent year 06
14.03.2005Renewal fee patent year 07
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Cited inInternational search[X]GB1075420  (GRUENENTHAL CHEMIE) [X] 1,2 * example 31 *;
 [Y]WO9214455  (UNIV ROCKEFELLER [US]) [Y] 1-16,18,26 * claims 1,2,6,11,12 *;
 [Y]EP0688771  (GRUENENTHAL GMBH [DE]) [Y] 1-16,18,26 * claims 1,2,5,6 *;
 [Y]US5635517  (MULLER GEORGE W [US], et al) [Y] 1-16,18,26* the whole document *;
 [X]WO9803502  (CELGENE CORP [US], et al) [X] 1-4,18 * claims 1,5-7 *;
 [PX]WO9854170  (CELGENE CORP [US], et al) [PX] 1-4,18 * page 10, line 3 - line 23; claims 6,10,12 *;
 [PX]  - MIYACHI H. ET AL., "Tumor necrosis factor-alpha production enhancing activity of substituted 3'-methylthalidomide: Influence of substituents at the phthaloyl moiety on the activity and stereoselectivity", CHEMICAL & PHARMACEUTICAL BULLETIN, (199807), vol. 46, no. 7, pages 1165 - 1168, XP002107774 [PX] 1,2,4,18 * see compounds (R)-9d and (S)-9d *
 [Y]  - NIWAYAMA S. ET AL., "Potent inhibition of tumor necrosis factor-.alpha. production by tetrafluorothalidomide and tetrafluorophthalimides", JOURNAL OF MEDICINAL CHEMISTRY, (19960101), vol. 39, no. 16, pages 3044 - 3045, XP002048231 [Y] 1-16,18,26 * the whole document *

DOI:   http://dx.doi.org/10.1021/jm960284r
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