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Extract from the Register of European Patents

EP About this file: EP2062052

EP2062052 - A METHOD OF DETERMINING ANALYTE CONCENTRATION [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  09.12.2011
Database last updated on 12.11.2024
Most recent event   Tooltip09.12.2011Application deemed to be withdrawnpublished on 11.01.2012  [2012/02]
Applicant(s)For all designated states
GE Healthcare Bio-Sciences AB
Björkgatan 30
75184 Uppsala / SE
[N/P]
Former [2009/22]For all designated states
GE Healthcare Bio-Sciences AB
Björkgatan 30
751 84 Uppsala / SE
Inventor(s)01 / BERLING, Henrik
Kamomillgatan 25
S-754 47 Uppsala / SE
02 / JARHEDE, Tanja
Edshammar
S-743 91 Storvreta / SE
03 / LARSSON, Anita
Järpvägen 27
S-756 53 Uppsala / SE
04 / ROOS, Håkan
Oslogatan 85
S-752 64 Uppsala / SE
 [2009/22]
Representative(s)Aldenbäck, Ulla Christina, et al
GE Healthcare Bio-Sciences AB
Patent Department
Björkgatan 30
751 84 Uppsala / SE
[N/P]
Former [2009/22]Aldenbäck, Ulla Christina, et al
GE Healthcare Bio-Sciences AB Patent Department Björkgatan 30
751 84 Uppsala / SE
Application number, filing date07808806.912.09.2007
[2009/22]
WO2007SE00792
Priority number, dateSE2006000189114.09.2006         Original published format: SE 0601891
US20060825664P14.09.2006         Original published format: US 825664 P
[2009/22]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2008033073
Date:20.03.2008
Language:EN
[2008/12]
Type: A1 Application with search report 
No.:EP2062052
Date:27.05.2009
Language:EN
The application published by WIPO in one of the EPO official languages on 20.03.2008 takes the place of the publication of the European patent application.
[2009/22]
Search report(s)International search report - published on:SE20.03.2008
(Supplementary) European search report - dispatched on:EP08.01.2010
ClassificationIPC:G01N33/543, G01N21/05, G01N33/564, G01N21/55, G01N33/53
[2009/52]
CPC:
G01N33/54306 (EP,US); G01N33/54366 (EP,US); G01N33/54393 (EP,US);
G01N15/1459 (EP,US); G01N15/1484 (EP,US)
Former IPC [2009/22]G01N33/543, G01N21/05, G01N33/564, G01N21/55
Designated contracting statesAT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   LV,   MC,   MT,   NL,   PL,   PT,   RO,   SE,   SI,   SK,   TR [2009/22]
Extension statesALNot yet paid
BANot yet paid
HRNot yet paid
MKNot yet paid
RSNot yet paid
TitleGerman:VERFAHREN ZUR BESTIMMUNG EINER ANALYTKONZENTRATION[2009/22]
English:A METHOD OF DETERMINING ANALYTE CONCENTRATION[2009/22]
French:PROCEDE DE DETERMINATION DE CONCENTRATION D'ANALYTE[2009/22]
Entry into regional phase13.02.2009National basic fee paid 
13.02.2009Search fee paid 
13.02.2009Designation fee(s) paid 
13.02.2009Examination fee paid 
Examination procedure13.02.2009Amendment by applicant (claims and/or description)
13.02.2009Examination requested  [2009/22]
01.03.2010Despatch of a communication from the examining division (Time limit: M06)
10.12.2010Reply to a communication from the examining division
10.03.2011Despatch of a communication from the examining division (Time limit: M04)
21.07.2011Application deemed to be withdrawn, date of legal effect  [2012/02]
24.08.2011Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time  [2012/02]
Divisional application(s)The date of the Examining Division's first communication in respect of the earliest application for which a communication has been issued is  01.03.2010
Request for further processing for:The application is deemed to be withdrawn due to failure to reply to the examination report
10.12.2010Request for further processing filed
10.12.2010Full payment received (date of receipt of payment)
Request granted
20.12.2010Decision despatched
Fees paidRenewal fee
25.09.2009Renewal fee patent year 03
27.09.2010Renewal fee patent year 04
26.09.2011Renewal fee patent year 05
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Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Documents cited:Search[A]US4703001  (VODIAN MORTON A [US], et al) [A] 1-15;
 [XI]  - MOXNESS M ET AL, "Immunogenicity Testing by Electrochemiluminescent Detection for Antibodies Directed against Therapeutic Human Monoclonal Antibodies", CLINICAL CHEMISTRY, AMERICAN ASSOCIATION FOR CLINICAL CHEMISTRY, WASHINGTON, DC, (20050101), vol. 51, no. 10, ISSN 0009-9147, pages 1983 - 1985, XP003019464 [X] 1-6,14-15 * p.1984 col.2 * [I] 7-13

DOI:   http://dx.doi.org/10.1373/clinchem.2005.053272
 [XI]  - SEIJI K ET AL, "An improved method for the detection of HIV antigen in the blood of carriers", JOURNAL OF VIROLOGICAL METHODS, ELSEVIER BV, NL, vol. 22, no. 2-3, ISSN 0166-0934, (19881201), pages 125 - 131, (19881201), XP023852141 [X] 1-5,14-15 * abstract * [I] 6-13

DOI:   http://dx.doi.org/10.1016/0166-0934(88)90095-X
 [XI]  - VON SYDOW M ET AL, Antigen detection in primary HIV infection., BRITISH MEDICAL JOURNAL (CLINICAL RESEARCH ED.) 23 JAN 1988, VOL. 296, NR. 6617, PAGE(S) 238 - 240, (19880123), ISSN 0267-0623, XP002554418 [X] 1-5,14-15 * abstract * [I] 6-13
 [A]  - NISHANIAN P ET AL, "A SIMPLE METHOD FOR IMPROVED ASSAY DEMONSTRATES THAT HIV P24 ANTIGEN IS PRESENT AS IMMUNE COMPLEXES IN MOST SERA FROM HIV-INFECTED INDIVIDUALS", JOURNAL OF INFECTIOUS DISEASES, UNIVERSITY OF CHICAGO PRESS, CHICAGO, IL, (19900101), vol. 162, no. 1, ISSN 0022-1899, pages 21 - 28, XP009039537 [A] 1-15
 [XI]  - CHEUNG C Y ET AL, High-pressure-mediated dissociation of immune complexes demonstrated in model systems., CLINICAL CHEMISTRY FEB 1998, VOL. 44, NR. 2, PAGE(S) 299 - 303, (199802), ISSN 0009-9147, XP002554419 [X] 1-2,5,14-15 * materials and methods * [I] 3-4,6-13
 [XI]  - LI QINGYOU ET AL, "Overcoming antigen masking of anti-amyloidbeta antibodies reveals breaking of B cell tolerance by virus-like particles in amyloidbeta immunized amyloid precursor protein transgenic mice", BMC NEUROSCIENCE, BIOMED CENTRAL, LONDON, GB, (20040608), vol. 5, no. 1, ISSN 1471-2202, page 21, XP021002853 [X] 1-2,5,14-15 * materials and methods * [I] 3-4,6-13

DOI:   http://dx.doi.org/10.1186/1471-2202-5-21
 [XI]  - UDAYKUMAR ET AL, "Acid pH-induced changes in the immunoreactivity of specific antigen and antibody in circulating immune complexes from tuberculosis sera", JOURNAL OF CLINICAL LABORATORY ANALYSIS, NEW YORK, NY, US, (19920101), vol. 6, no. 4, ISSN 0887-8013, pages 194 - 200, XP009125293 [X] 1-5,14-15 * discussion * [I] 6-13

DOI:   http://dx.doi.org/10.1002/jcla.1860060406
International search[X]US4459359  (NEURATH A ROBERT [US]);
 [X]EP0375439  (SYNTEX INC [US]);
 [A]EP0440044  (ABBOTT LAB [US]);
 [A]US5219730  (POTOCNJAK PEDRO [CL], et al);
 [A]US5256541  (POULETTY PHILIPPE J [US], et al);
 [A]US2003003503  (TSAI TENLIN S [US], et al);
 [X]  - MOXNESS M. ET AL., "Immunogenicity Testing by Electrochemiluminescent Detection for Antibodies Directed against Therapeutic Human Monoclonal Antibodies", CLINICAL CHEMISTRY, (2005), vol. 51, no. 10, pages 1983 - 1985, XP003019464

DOI:   http://dx.doi.org/10.1373/clinchem.2005.053272
 [A]  - TOMIMORI-YAMASHITA J. ET AL., "Antibody-based enzyme-linked immunosorbent assay for determination of anti-PGL-I specific circulating immune complex in leprosy patients", MEDLINE, Database accession no. (10603715), XP003019465
    [ ] - LIPROSY REVIEW, (199909), vol. 70, no. 3, pages 261 - 271
 [A]  - NEDELKOV D. ET AL., "Detection of bound and free IGF-1 and IGF-2 in human plasma via biomolecular interaction analysis mass spectrometry", FEBS LETTERS, (2003), vol. 536, pages 130 - 134, XP004409815

DOI:   http://dx.doi.org/10.1016/S0014-5793(03)00042-5
ExaminationGB2278195
 WO9609319
    - JASON-MOLLER LAURE ET AL, "Overview of Biacore systems and their applications", CURRENT PROTOCOLS IN PROTEIN SCIENCE, JOHN WILEY & SONS, INC, US, (20060901), no. SUPPL. 45, ISSN 1934-3655, pages 19.13.1 - 19.13.14, XP002556429
by applicant   - TOMIMORI-YAMASHITA, J. ET AL., LEPR. REV., (1999), vol. 70, pages 261 - 271
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.