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Extract from the Register of European Patents

EP About this file: EP1602369

EP1602369 - Bupropion Metabolites for treating anxiety [Right-click to bookmark this link]
Former [2005/49]Bupropion Metabolites and Methods of their Synthesis and Use
[2009/22]
StatusNo opposition filed within time limit
Status updated on  11.02.2011
Database last updated on 03.10.2024
Most recent event   Tooltip28.09.2012Lapse of the patent in a contracting state
New state(s): LU
published on 31.10.2012  [2012/44]
Applicant(s)For all designated states
SEPRACOR, INC.
84 Waterford Drive
Marlborough, MA 01752 / US
[2010/14]
Former [2005/49]For all designated states
SEPRACOR, INC.
84 waterford Drive
Marlborough, MA 01752 / US
Inventor(s)01 / Fang, Qun, K
35 Atwood Street
02181, Wellesley / US
02 / Senanayake, Chrisantha, H
12 Isabel's Way
Brookfield, CT 06804 / US
03 / Grover, Paul
4 Warwick Road
02038, Franklin / US
 [2006/13]
Former [2005/49]01 / Fang, Qun, K
35 Atwood Street
02181, Wellesley / US
02 / Senanayake, Chrisantha, H
11 Old Farm Circle
01545, Shrewsbury / US
03 / Grover, Paul
4 Warwick Road
02038, Franklin / US
Representative(s)Killin, Stephen James, et al
Venner Shipley LLP
200 Aldersgate
London EC1A 4HD / GB
[N/P]
Former [2005/49]Killin, Stephen James, et al
Venner Shipley LLP 20 Little Britain
London EC1A 7DH / GB
Application number, filing date05106426.923.08.2000
[2005/49]
Priority number, dateUS2000051024122.02.2000         Original published format: US 510241
US2000064072518.08.2000         Original published format: US 640725
[2005/49]
Filing languageEN
Procedural languageEN
PublicationType: A2 Application without search report 
No.:EP1602369
Date:07.12.2005
Language:EN
[2005/49]
Type: A3 Search report 
No.:EP1602369
Date:14.02.2007
[2007/07]
Type: B1 Patent specification 
No.:EP1602369
Date:07.04.2010
Language:EN
[2010/14]
Search report(s)(Supplementary) European search report - dispatched on:EP15.01.2007
ClassificationIPC:A61K31/5375, A61K31/137, A61P25/24, A61P25/34, A61P25/20
[2006/47]
CPC:
A61K31/537 (EP,US); A61K31/5375 (EP,KR,US); A61K31/00 (EP,US);
A61K31/135 (EP,US); A61K31/137 (EP,US); A61K31/165 (EP,US);
A61K31/415 (EP,US); A61K31/43 (EP,US); A61K31/435 (EP,US);
A61K31/46 (EP,US); A61K31/465 (EP,US); A61K31/50 (EP,US);
A61K31/53 (EP,US); A61K31/535 (EP,US); A61K45/06 (EP,US);
A61P1/08 (EP); A61P13/00 (EP); A61P13/10 (EP);
A61P15/00 (EP); A61P15/10 (EP); A61P25/00 (EP);
A61P25/04 (EP); A61P25/08 (EP); A61P25/16 (EP);
A61P25/18 (EP); A61P25/20 (EP); A61P25/24 (EP);
A61P25/28 (EP); A61P25/34 (EP); A61P43/00 (EP);
C07C213/00 (EP,US); C07C215/30 (EP,US); C07C225/16 (EP,US);
C07C45/511 (EP,US); C07C45/63 (EP,US); C07C49/84 (EP,US);
C07C69/76 (EP,US); C07D265/32 (EP,US); C07B2200/07 (EP,US) (-)
C-Set:
A61K31/135, A61K2300/00 (US,EP);
A61K31/137, A61K2300/00 (US,EP);
A61K31/165, A61K2300/00 (US,EP);
A61K31/415, A61K2300/00 (US,EP);
A61K31/435, A61K2300/00 (US,EP);
A61K31/43, A61K2300/00 (US,EP);
A61K31/465, A61K2300/00 (US,EP);
A61K31/46, A61K2300/00 (US,EP);
A61K31/50, A61K2300/00 (US,EP);
A61K31/535, A61K2300/00 (EP,US);
A61K31/5375, A61K2300/00 (EP,US);
A61K31/53, A61K2300/00 (EP,US);
C07C45/511, C07C49/82 (US,EP);
C07C45/63, C07C49/80 (US,EP)
(-)
Former IPC [2005/49]A61K31/137, A61P25/24, A61P25/34, A61P25/20, A61K31/5375
Designated contracting statesAT,   BE,   CH,   CY,   DE,   DK,   ES,   FI,   FR,   GB,   GR,   IE,   IT,   LI,   LU,   MC,   NL,   PT,   SE [2005/49]
Extension statesAL13.07.2005
LT13.07.2005
MK13.07.2005
RO13.07.2005
SI13.07.2005
TitleGerman:Bupropion Metaboliten zur Behandlung von Angstzuständen[2010/14]
English:Bupropion Metabolites for treating anxiety[2009/22]
French:Métabolites du bupropione pour traiter l'anxiété[2009/22]
Former [2005/49]Bupropion Metaboliten und Verfahren zu ihrer Synthese und Behandlung
Former [2005/49]Bupropion Metabolites and Methods of their Synthesis and Use
Former [2005/49]Métabolites du bupropione et méthodes pour leur synthèse et utilisation
Examination procedure13.07.2005Examination requested  [2005/49]
08.08.2007Despatch of a communication from the examining division (Time limit: M06)
27.12.2007Reply to a communication from the examining division
25.01.2008Despatch of a communication from the examining division (Time limit: M06)
20.11.2008Reply to a communication from the examining division
18.05.2009Communication of intention to grant the patent
18.11.2009Despatch of communication that the application is deemed to be withdrawn, reason: fee for grant / fee for printing not paid in time
27.01.2010Fee for grant paid
27.01.2010Fee for publishing/printing paid
Parent application(s)   TooltipEP00957684.4  / EP1259243
Opposition(s)10.01.2011No opposition filed within time limit [2011/11]
Request for further processing for:The application is deemed to be withdrawn due to failure to fulfill actions required for granting the patent
27.01.2010Request for further processing filed
27.01.2010Full payment received (date of receipt of payment)
Request granted
09.02.2010Decision despatched
The application is deemed to be withdrawn due to failure to reply to the examination report
20.11.2008Request for further processing filed
20.11.2008Full payment received (date of receipt of payment)
Request granted
10.12.2008Decision despatched
Fees paidRenewal fee
13.07.2005Renewal fee patent year 03
13.07.2005Renewal fee patent year 04
13.07.2005Renewal fee patent year 05
12.08.2005Renewal fee patent year 06
14.08.2006Renewal fee patent year 07
14.08.2007Renewal fee patent year 08
28.08.2008Renewal fee patent year 09
25.08.2009Renewal fee patent year 10
Opt-out from the exclusive  Tooltip
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Patent Court
See the Register of the Unified Patent Court for opt-out data
Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Lapses during opposition  TooltipAT07.04.2010
BE07.04.2010
DK07.04.2010
FI07.04.2010
IT07.04.2010
SE07.04.2010
CY21.04.2010
GR08.07.2010
ES18.07.2010
PT09.08.2010
IE23.08.2010
LU23.08.2010
MC31.08.2010
[2012/44]
Former [2011/36]AT07.04.2010
BE07.04.2010
DK07.04.2010
FI07.04.2010
IT07.04.2010
SE07.04.2010
CY21.04.2010
GR08.07.2010
ES18.07.2010
PT09.08.2010
IE23.08.2010
MC31.08.2010
Former [2011/15]AT07.04.2010
BE07.04.2010
DK07.04.2010
FI07.04.2010
IT07.04.2010
SE07.04.2010
CY21.04.2010
GR08.07.2010
ES18.07.2010
PT09.08.2010
MC31.08.2010
Former [2011/08]AT07.04.2010
DK07.04.2010
FI07.04.2010
SE07.04.2010
CY21.04.2010
GR08.07.2010
ES18.07.2010
PT09.08.2010
Former [2011/07]AT07.04.2010
DK07.04.2010
FI07.04.2010
SE07.04.2010
CY21.04.2010
GR08.07.2010
ES18.07.2010
Former [2011/03]AT07.04.2010
FI07.04.2010
SE07.04.2010
CY21.04.2010
GR08.07.2010
ES18.07.2010
Former [2011/01]AT07.04.2010
FI07.04.2010
SE07.04.2010
GR08.07.2010
ES18.07.2010
Former [2010/52]AT07.04.2010
FI07.04.2010
SE07.04.2010
ES18.07.2010
Former [2010/46]ES18.07.2010
Documents cited:Search[X]WO9937305  (GLAXO GROUP LTD [GB], et al) [X] 1-4,7-9,12,19,20,22-30 * page 1, line 1 - line 18 * * page 4, line 20 - page 5, line 29 * * page 2 - page 3 * * claims 1-6 *;
 [X]  - POLLOCK, B. G. ET AL, "Bupropion plasma levels and CYP2D6 phenotype", THER. DRUG MONIT. (1996), 18(5), 581-585, (1996), XP001040975 [X] 1-9,12,19,20,22-30,53-61 * page 582, column 2, paragraph 2 * * page 581, column 2, paragraph 3 *

DOI:   http://dx.doi.org/10.1097/00007691-199610000-00010
 [X]  - MUSSO ET AL, "Synthesis and evaluation of the antidepressant activity of the enentiomers of bupropion", CHIRALITY, WILEY-LISS, NEW YORK, US, (1993), vol. 5, no. 7, ISSN 0899-0042, pages 495 - 500, XP002107656 [X] 1-9,12,19,20,22-30,53-61 * page 495, column 1, paragraph 1 *

DOI:   http://dx.doi.org/10.1002/chir.530050704
 [X]  - PERUMAL, A. S. ET AL, "Down-regulation of.beta.-receptors by bupropion and its major metabolite in mouse brain", NEUROPHARMACOLOGY (1986), 25(12), 1323-6, (1986), XP001040976 [X] 1-9,12,19,20,22-30,53-61 * page 1323, column 1, paragraph 1 *

DOI:   http://dx.doi.org/10.1016/0028-3908(86)90103-6
 [X]  - LAIZURE, S. CASEY ET AL, "Stability of bupropion and its major metabolites in human plasma", THER. DRUG MONIT. (1985), 7(4), 447-50, (1985), XP001040981 [X] 1-9,12,19,20,22-30,53-61 * page 447, column 1, paragraph 2 - column 2, paragraph 1 * * figure 1 *
 [X]  - KELLEY JAMES L ET AL, "-2-(3,5-difluorophenyl)-3,5-dimethyl-2-morpholinol: A novel antidepressant agent and selective inhibitor of norepinephrine uptake", JOURNAL OF MEDICINAL CHEMISTRY, AMERICAN CHEMICAL SOCIETY. WASHINGTON, US, (1996), vol. 39, no. 2, ISSN 0022-2623, pages 347 - 349, XP002164358 [X] 1-9,12,19,20,22-30,53-61 * page 347, column 1, paragraph 2 *

DOI:   http://dx.doi.org/10.1021/jm950630p
 [PX]  - ADEOYE, O. M. ET AL, "Bupropion plasma concentration and antidepressant response in elderly patients: A prospective, randomized, double-blind study", INT. J. GERIATR. PSYCHOPHARMACOL. (2000), 2(3), 132-136, (2000), XP001040979 [PX] 1-9,12,19,20,22-30,54-61 * page 132, column 2, paragraph 3 *
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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.