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EP3283647
European procedure
Extract from the Register of European Patents
EP About this file: EP3283647
| EP3283647 - A METHOD FOR NON-INVASIVE PRENATAL DETECTION OF FETAL CHROMOSOME ANEUPLOIDY FROM MATERNAL BLOOD [Right-click to bookmark this link] | Status | No opposition filed within time limit Status updated on 13.09.2019 Database last updated on 28.05.2024 | |
| Former | The patent has been granted Status updated on 05.10.2018 | ||
| Former | Grant of patent is intended Status updated on 19.07.2018 | ||
| Former | Examination is in progress Status updated on 15.09.2017 | ||
| Former | unknown Status updated on 03.02.2017 | Most recent event Tooltip | 24.06.2022 | Change - lapse in a contracting state ???moredetails.lapse.edited??? AL | published on 27.07.2022 [2022/30] | Applicant(s) | For all designated states Trisomytest, s.r.o. Ilkovicova 8 841 04 Bratislava - Karlova Ves / SK | [2018/24] |
| Former [2018/08] | For all designated states Trisomytest, s.r.o. Stefanovi ova 12 811 04 Bratislava / SK | Inventor(s) | 01 /
DURIS, Frantisek Bratislavská 13 010 01 Zilina / SK | 02 /
BUDIS, Jaroslav Bradácova 5 851 01 Bratislava / SK | 03 /
SZEMES, Tomás Studenohorská 73 841 03 Bratislava / SK | 04 /
MINÁRIK, Gabriel Záhumenice 783/78 951 48 Jarok / SK | [2018/08] | Representative(s) | Hak, Roman Hak, Janecek & Svestka Patent and Trademark Attorneys U Pruhonu 5 170 00 Praha 7 / CZ | [2018/08] | Application number, filing date | 16734594.1 | 23.06.2016 | [2018/08] | WO2016EP64604 | Filing language | EN | Procedural language | EN | Publication | Type: | A1 Application with search report | No.: | WO2017220156 | Date: | 28.12.2017 | Language: | EN | [2017/52] | Type: | A1 Application with search report | No.: | EP3283647 | Date: | 21.02.2018 | Language: | EN | The application published by WIPO in one of the EPO official languages on 28.12.2017 takes the place of the publication of the European patent application. | [2018/08] | Type: | B1 Patent specification | No.: | EP3283647 | Date: | 07.11.2018 | Language: | EN | [2018/45] | Search report(s) | International search report - published on: | EP | 28.12.2017 | Classification | IPC: | C12Q1/68, G06F19/18, G06F19/22 | [2018/08] | CPC: |
C12Q1/6809 (EP,EA);
G16B20/10 (EP,EA,RU,US);
C12Q1/68 (RU);
G16B20/00 (EP,EA);
G16B20/20 (EP,EA,RU,US);
G16B30/00 (EP,EA,RU,US);
C12Q1/6883 (EP,EA)
(-)
| C-Set: |
C12Q1/6809, C12Q2537/16, C12Q2537/165 (EP)
| Designated contracting states | AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LI, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR [2018/08] | Extension states | BA | Not yet paid | ME | Not yet paid | Validation states | MA | Not yet paid | MD | Not yet paid | Title | German: | VERFAHREN ZUM NICHT-INVASIVEN PRÄNATALEN NACHWEIS VON FÖTALER CHROMOSOMENANEUPLOIDIE AUS MÜTTERLICHEM BLUT | [2018/08] | English: | A METHOD FOR NON-INVASIVE PRENATAL DETECTION OF FETAL CHROMOSOME ANEUPLOIDY FROM MATERNAL BLOOD | [2018/08] | French: | METHODE DE DETECTION PRENATALE NON-INVASIVE D'ANEUPLOIDIE CHROMOSOMIQUE FETALE DANS LE SANG MATERNEL | [2018/32] |
| Former [2018/08] | PROCÉDÉ DE DÉTECTION PRÉNATALE NON INVASIVE DE L'ANEUPLOÏDIE CHROMOSOMIQUE F TALE À PARTIR DU SANG MATERNEL | Entry into regional phase | 02.02.2017 | National basic fee paid | 02.02.2017 | Designation fee(s) paid | 02.02.2017 | Examination fee paid | Examination procedure | 01.02.2017 | Amendment by applicant (claims and/or description) | 01.02.2017 | Date on which the examining division has become responsible | 02.02.2017 | Examination requested [2018/08] | 04.09.2017 | Despatch of a communication from the examining division (Time limit: M04) | 19.12.2017 | Reply to a communication from the examining division | 20.02.2018 | Despatch of a communication from the examining division (Time limit: M04) | 02.05.2018 | Reply to a communication from the examining division | 20.07.2018 | Communication of intention to grant the patent | 14.09.2018 | Fee for grant paid | 14.09.2018 | Fee for publishing/printing paid | 17.09.2018 | Receipt of the translation of the claim(s) | Opposition(s) | 08.08.2019 | No opposition filed within time limit [2019/42] | Fees paid | Renewal fee | 06.06.2018 | Renewal fee patent year 03 |
| Opt-out from the exclusive Tooltip competence of the Unified 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 Tooltip | AL | 07.11.2018 | [2022/30] |
| Former [2022/23] | deleted | ||
| Former [2019/50] | AL | 07.11.2018 | |
| Former [2019/49] | deleted | ||
| Former [2019/26] | AL | 07.11.2018 | Cited in | International search | [XDA] - CHIU ROSSA W K ET AL, "Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma", PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES, NATIONAL ACADEMY OF SCIENCES, US, vol. 105, no. 51, doi:10.1073/PNAS.0810641105, ISSN 0027-8424, (20081223), pages 20458 - 20463, (20081210), XP002620454 [XD] 12,13 * abstract * * Materials and methods * [A] 1-11 DOI: http://dx.doi.org/10.1073/pnas.0810641105 | [ ] - R. W. K. Chiu ET AL, "Supplementary Information for XP002620454 (Title: Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma)", Proceedings of the National Academy of Sciences, US, (20081210), vol. 105, no. 51, doi:10.1073/pnas.0810641105, ISSN 0027-8424, pages 20458 - 20463, XP055024153 DOI: http://dx.doi.org/10.1073/pnas.0810641105 | [XDA] - LAU TZE KIN ET AL, "Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing", THE JOURNAL OF MATERNAL FETAL & NEONATAL MEDICINE : THE OFFICIAL JOURNAL OF THE EUROPEAN ASSOCIATION OF PERINATAL MEDICINE, THE FEDERATION OF ASIA AND OCEANIA PERINATAL SOCIETIES, THE INTERNATIONAL SOCIETY OF PERINATAL OBSTETRICIANS, INFORMA HEALTHCA, (20120801), vol. 25, no. 8, doi:10.3109/14767058.2011.635730, ISSN 1057-0802, pages 1370 - 1374, XP008164835 [XD] 12,13 * abstract * * Methods * [A] 1-11 DOI: http://dx.doi.org/10.3109/14767058.2011.635730 | [XDA] - A. J. SEHNERT ET AL, "Optimal Detection of Fetal Chromosomal Abnormalities by Massively Parallel DNA Sequencing of Cell-Free Fetal DNA from Maternal Blood", CLINICAL CHEMISTRY, (20110701), vol. 57, no. 7, doi:10.1373/clinchem.2011.165910, ISSN 0009-9147, pages 1042 - 1049, XP055035087 [XD] 12,13 * abstract * * Materials and methods * [A] 1-11 DOI: http://dx.doi.org/10.1373/clinchem.2011.165910 | [XA] - H. CHRISTINA FAN ET AL, "Sensitivity of Noninvasive Prenatal Detection of Fetal Aneuploidy from Maternal Plasma Using Shotgun Sequencing Is Limited Only by Counting Statistics", PLOS ONE, (20100101), vol. 5, no. 5, doi:10.1371/journal.pone.0010439, ISSN 1932-6203, page e10439, XP055026436 [X] 12,13 * abstract * * Methods * [A] 1-11 DOI: http://dx.doi.org/10.1371/journal.pone.0010439 |