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Extract from the Register of European Patents

EP About this file: EP0038567

EP0038567 - Deazapurine nucleoside, formulations thereof, and use thereof in therapy [Right-click to bookmark this link]
StatusNo opposition filed within time limit
Status updated on  22.07.1988
Database last updated on 02.11.2024
Most recent event   Tooltip22.07.1988No opposition filed within time limitpublished on 07.09.1988 [1988/36]
Applicant(s)For all designated states
THE WELLCOME FOUNDATION LIMITED
Unicorn House 160 Euston Road P.O. Box 129
London NW1 2BP / GB
[N/P]
Former [1981/43]For all designated states
THE WELLCOME FOUNDATION LIMITED
Unicorn House 160 Euston Road
London NW1 2BP / GB
Inventor(s)01 / Vinegar, Ralph
5337 Thayer Drive
Raleigh North Carolina 27609 / US
02 / Wolberg, Gerald
1109 Troon Court
Cary North Carolina 27511 / US
[1981/43]
Representative(s)Berg, Wilhelm, et al
Mauerkircherstrasse 45
81679 München / DE
[N/P]
Former [1987/13]Berg, Wilhelm, Dr., et al
Mauerkircherstrasse 45
D-81679 München / DE
Former [1981/43]Berg, Wilhelm, Dr.
Patentanwälte Dr. Berg Dipl.-Ing. Stapf Dipl.-Ing. Schwabe Dr. Dr. Sandmair Postfach 86 02 45 Stuntzstrasse 16
D-8000 München 86 / DE
Application number, filing date81103043.622.04.1981
[1981/43]
Priority number, dateGB1980001341123.04.1980         Original published format: GB 8013411
[1981/43]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report 
No.:EP0038567
Date:28.10.1981
Language:EN
[1981/43]
Type: B1 Patent specification 
No.:EP0038567
Date:23.09.1987
Language:EN
[1987/39]
Search report(s)(Supplementary) European search report - dispatched on:EP13.07.1981
ClassificationIPC:A61K31/70, C07H19/04
[1981/43]
CPC:
C07H19/052 (EP); A61P29/00 (EP)
Designated contracting statesBE,   CH,   DE,   FR,   GB,   LI,   LU,   NL,   SE [1981/43]
TitleGerman:Deazapurin-Nukleosid, es enthaltende Zusammensetzungen und seine therapeutische Verwendung[1981/43]
English:Deazapurine nucleoside, formulations thereof, and use thereof in therapy[1981/43]
French:Déazapurine nucléoside, compositions le contenant et son utilisation comme thérapeutique[1981/43]
File destroyed:15.01.2000
Examination procedure21.04.1982Examination requested  [1982/27]
27.08.1982Despatch of a communication from the examining division (Time limit: M06)
17.02.1983Reply to a communication from the examining division
01.07.1983Despatch of a communication from the examining division (Time limit: M06)
27.12.1983Reply to a communication from the examining division
25.02.1985Despatch of a communication from the examining division (Time limit: M06)
20.08.1985Reply to a communication from the examining division
15.10.1985Despatch of a communication from the examining division (Time limit: M06)
16.04.1986Reply to a communication from the examining division
11.07.1986Despatch of communication of intention to grant (Approval: )
05.08.1986Communication of intention to grant the patent
02.10.1986Fee for grant paid
02.10.1986Fee for publishing/printing paid
Opposition(s)24.06.1988No opposition filed within time limit [1988/36]
Fees paidRenewal fee
31.03.1983Renewal fee patent year 03
22.03.1984Renewal fee patent year 04
27.03.1985Renewal fee patent year 05
13.03.1986Renewal fee patent year 06
05.03.1987Renewal fee patent year 07
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Documents cited:SearchUS4148888  [ ] (CANTONI GIULIO L, et al);
 EP0010668  [ ] (WELLCOME FOUND [GB])
    [ ] - CHEMICAL ABSTRACTS, Vol. 70, No. 11, March 16, 1969. page 377, Abstract 47771n Columbus, Ohio, USA Y. MIZUNO et al. "Synthetic Studies of Potential Antimetabolites. XII. Synthesis of 4-Substituted 1-(beta-D-Ribofuranosyl)-1Himidazo-(4,5-c)Pyridines" & Chem. Pharm. Bull, (Tokyo) 1968, 16(10), 2011-17 * Abstract and Chemical Abstracts Eight Collective Index, Volumes 66-75, Subjects Glycope-Indena paes 15641s: 1H-Imidazo(4,5-c) Pyridine-,4-Amino-1-beta-D-Ribofuralosy- *
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.