EP1307588 - Method for diagnosing or determining a risk for psychosis comprising determining an heterozygous mutation of methylenetetrahydrofolate reductase (MTHFR) [Right-click to bookmark this link] | |||
Former [2003/19] | cDNA FOR HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE AND USES THEREOF | ||
[2008/18] | Status | No opposition filed within time limit Status updated on 27.11.2009 Database last updated on 18.10.2024 | Most recent event Tooltip | 27.11.2009 | No opposition filed within time limit | published on 30.12.2009 [2009/53] | Applicant(s) | For all designated states McGill University 3550 University Street Montreal Quebec H3A 2A7 / CA | [2009/04] |
Former [2003/19] | For all designated states McGill University 3550 University Street Montreal, Quebec H3A 2A7 / CA | Inventor(s) | 01 /
ROZEN, Rima 9 Fairfield Crescent Montreal West, Quebec H4X 1R5 / CA | [2003/19] | Representative(s) | Bösl, Raphael Konrad Patentanwälte Isenbruck Bösl Hörschler PartG mbB Eastsite One Seckenheimer Landstraße 4 68163 Mannheim / DE | [N/P] |
Former [2008/38] | Bösl, Raphael Konrad Patentanwälte Isenbruck Bösl Hörschler Wichmann Huhn Prinzregentenstrasse 68 81675 München / DE | ||
Former [2003/19] | Bösl, Raphael, Dr. rer. nat., Dipl.-Chem. Patentanwälte Isenbruck Bösl Hörschler Wichmann Huhn Postfach 860 880 81635 München / DE | Application number, filing date | 01944818.2 | 12.06.2001 | [2003/19] | WO2001CA00867 | Priority number, date | US20000592595 | 12.06.2000 Original published format: US 592595 | [2003/19] | Filing language | EN | Procedural language | EN | Publication | Type: | A2 Application without search report | No.: | WO0196598 | Date: | 20.12.2001 | Language: | EN | [2001/51] | Type: | A2 Application without search report | No.: | EP1307588 | Date: | 07.05.2003 | Language: | EN | The application published by WIPO in one of the EPO official languages on 20.12.2001 takes the place of the publication of the European patent application. | [2003/19] | Type: | B1 Patent specification | No.: | EP1307588 | Date: | 21.01.2009 | Language: | EN | [2009/04] | Search report(s) | International search report - published on: | EP | 13.03.2003 | Classification | IPC: | C12Q1/68, A61K31/00, A61P25/18 | [2003/19] | CPC: |
C12N9/0028 (EP,US);
A61P25/00 (EP);
A61P25/04 (EP);
A61P25/06 (EP);
A61P25/08 (EP);
A61P25/14 (EP);
A61P25/16 (EP);
A61P25/18 (EP);
A61P25/22 (EP);
A61P25/24 (EP);
A61P25/28 (EP);
A61P7/04 (EP);
A61P9/10 (EP);
C12N9/0026 (EP,US);
C12Q1/6883 (EP,US);
C12Y105/0102 (EP,US);
A61K38/00 (EP,US);
A61K48/00 (EP,US);
C12Q2600/156 (EP,US)
(-)
| Designated contracting states | DE, GB [2004/21] |
Former [2003/19] | AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, LI, LU, MC, NL, PT, SE, TR | Extension states | AL | Not yet paid | LT | Not yet paid | LV | Not yet paid | MK | Not yet paid | RO | Not yet paid | SI | Not yet paid | Title | German: | Methode zur Diagnose von oder zur Bestimmung des Risikos für Psychose beinhaltend die Bestimmung einer heterozygoten Mutation der Methylentetrahydrolfolatreduktase (MTHFR) | [2008/18] | English: | Method for diagnosing or determining a risk for psychosis comprising determining an heterozygous mutation of methylenetetrahydrofolate reductase (MTHFR) | [2008/18] | French: | Méthode de diagnostic ou de prédiction d'un risque d'une psychose comprenant la détermination de mutation hétérozygote de la méthylène tetra hydrofolate réductase (MTHFR) | [2008/18] |
Former [2003/19] | CDNA FÜR HUMANE METHYLENTETRAHYDROFOLAT REDUKTASE UND VERWENDUNGEN DERSELBEN | ||
Former [2003/19] | cDNA FOR HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE AND USES THEREOF | ||
Former [2003/19] | ADNC DE REDUCTASE DE METHYLENE TETRAHYDROFOLATE HUMAINE ET SES UTILISATIONS | Entry into regional phase | 13.01.2003 | National basic fee paid | 13.01.2003 | Designation fee(s) paid | 13.01.2003 | Examination fee paid | Examination procedure | 29.12.2001 | Request for preliminary examination filed International Preliminary Examining Authority: EP | 13.01.2003 | Amendment by applicant (claims and/or description) | 13.01.2003 | Examination requested [2003/19] | 01.12.2005 | Despatch of a communication from the examining division (Time limit: M04) | 10.04.2006 | Reply to a communication from the examining division | 24.05.2006 | Despatch of a communication from the examining division (Time limit: M06) | 04.12.2006 | Reply to a communication from the examining division | 01.06.2007 | Despatch of a communication from the examining division (Time limit: M06) | 11.12.2007 | Reply to a communication from the examining division | 14.07.2008 | Communication of intention to grant the patent | 27.10.2008 | Fee for grant paid | 27.10.2008 | Fee for publishing/printing paid | Opposition(s) | 22.10.2009 | No opposition filed within time limit [2009/53] | Fees paid | Renewal fee | 24.09.2003 | Renewal fee patent year 03 | 23.06.2004 | Renewal fee patent year 04 | 21.06.2005 | Renewal fee patent year 05 | 28.06.2006 | Renewal fee patent year 06 | 27.06.2007 | Renewal fee patent year 07 | 27.03.2008 | Renewal fee patent year 08 | Penalty fee | Additional fee for renewal fee | 30.06.2003 | 03   M06   Fee paid on   24.09.2003 |
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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. | Cited in | International search | [A]WO9533054 (UNIV MCGILL [CA], et al) [A] 1-69 * the whole document *; | [A]WO9961014 (SEPRACOR INC [US]) [A] 52-69 * the whole document *; | [PX]WO0071754 (UNIV NEW JERSEY MED [US], et al) [PX] 21-52 * page 67; claim 3; table 13 *; | [X] - JOOBER R ET AL, "Association between the methyltetrahydrofolate reductase 667C.T missense mutation and schizophrenia", CHEMICAL ABSTRACTS, (20010205), vol. 134, no. 6, Database accession no. 69744y, page 514, column 1, XP002221407 [X] 1-69 * abstract * | [ ] - JOOBER R ET AL, MOL. PSYCHIATRY, (200005), vol. 5, no. 3, pages 323 - 326 | [X] - REGLAND B ET AL, "HOMOZYGOUS THERMOLABILE METHYLENETETRAHYDROFOLATE REDUCTASE IN SCHIZOPHRENIA-LIKE PSYCHOSIS", JOURNAL OF NEURAL TRANSMISSION, SPRINGER VERLAG, VIENNA, AT, (1997), vol. 104, no. 8/9, ISSN 0300-9564, pages 931 - 941, XP001031228 [X] 21-69 * the whole document * DOI: http://dx.doi.org/10.1007/BF01285561 | [X] - KUNUGI H ET AL, "C677T POLYMORPHISM IN METHYLENETETRAHYDROFOLATE REDUCTASE GENE AND PYSCHOSES", MOLECULAR PSYCHIATRY, BASINGSTOKE, GB, (1998), vol. 3, no. 5, ISSN 1359-4184, pages 435 - 437, XP001031246 [X] 21-52 * the whole document * DOI: http://dx.doi.org/10.1038/sj.mp.4000390 | [X] - ARINAMI T ET AL, "METHYLENETETRAHYDROFOLATE REDUCTASE VARIANT AND SCHIZOPHRENIA/DEPRESSION", AMERICAN JOURNAL OF MEDICAL GENETICS, NEW YORK,NY, US, (1997), vol. 74, no. 5, pages 526 - 528, XP001031351 [X] 21-69 * the whole document * DOI: http://dx.doi.org/10.1002/(SICI)1096-8628(19970919)74:5<526::AID-AJMG14>3.0.CO;2-E | [A] - GOYETTE P ET AL, "SEVERE AND MILD MUTATIONS IN CIS FOR THE METHYLENETETRAHYDROFOLATE RUDUCTASE (MTHFR) GENE, AND DESCRIPTION OF FIVE NOVEL MUTATIONS IN MTHFR", AMERICAN JOURNAL OF HUMAN GENETICS, UNIVERSITY OF CHICAGO PRESS, CHICAGO,, US, (19961201), vol. 59, no. 6, ISSN 0002-9297, pages 1268 - 1275, XP000672651 [A] 1-52 * the whole document * | [A] - GOYETTE P ET AL, "SEVEN NOVEL MUTATIONS IN THE METHYLENETETRAHYDROFOLATE REDUCTASE GENE AND GENOTYPE/PHENOTYPE CORRELATIONS IN SEVERE METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY", AMERICAN JOURNAL OF HUMAN GENETICS, UNIVERSITY OF CHICAGO PRESS, CHICAGO,, US, (19950501), vol. 56, no. 5, ISSN 0002-9297, pages 1052 - 1059, XP000198176 [A] 21-52 * the whole document * | [A] - PEREIRA P ET AL, "Loss of heterozygosity of methylenetetrahydrofolate reductase in colon carcinomas", ONCOLOGY REPORTS, NATIONAL HELLENIC RESEARCH FOUNDATION, ATHENS, GR, (1999), vol. 6, no. 6, ISSN 1021-335X, pages 597 - 599, XP002121824 [A] 1-20,52-69 * the whole document * | Examination | WO9634980 | - JOOBER ET AL., "Association between the methylene tetrahydrofolate reductase 677C->T missense mutation and schizophrenia", MOLECULAR PSYCHIATRY, (20000505), vol. 5, pages 323 - 326 | - REGLAND B. ET AL, "Homocysteinemia and schizophrenia as a case of methylation deficiency", J. NEURAL TRANSM., (1994), vol. 98, doi:doi:10.1007/BF01277017, pages 143 - 152, XP001031308 DOI: http://dx.doi.org/10.1007/BF01277017 | - FREEMAN J.M. ET AL, "Folate-responsive homocystinuria and "schizophrenia"", N. ENGL. J. MED., (1975), vol. 292, no. 10, pages 491 - 496, XP008064272 | - SAZCI A ET AL, "Methylenetetrahydrofolate reductase gene polymorphisms in pateints with schizophrenia", MOLECULAR BRAIN RESEARCH, (2003), vol. 117, pages 104 - 107 |