EP3792923 - METHOD AND DEVICE FOR EXCHANGING INFORMATION REGARDING THE CLINICAL IMPLICATIONS OF GENOMIC VARIATIONS [Right-click to bookmark this link] | Status | The application has been withdrawn Status updated on 13.10.2023 Database last updated on 16.07.2024 | |
Former | Examination is in progress Status updated on 09.06.2023 | ||
Former | Request for examination was made Status updated on 12.02.2021 | Most recent event Tooltip | 13.10.2023 | Withdrawal of application | published on 15.11.2023 [2023/46] | Applicant(s) | For all designated states Siemens Healthcare GmbH Henkestraße 127 91052 Erlangen / DE | [2021/11] | Inventor(s) | 01 /
Dietrich, Carsten Gärtnerstraße 12 90408 Nürnberg / DE | 02 /
Frings, Oliver Stettiner Straße 1a 91058 Erlangen / DE | 03 /
Kubala, Eugen Mohrstr. 8 80939 München / DE | 04 /
Neumann, Dominik Allee am Röthelheimpark 44 91052 Erlangen / DE | 05 /
Weiss, Maximilian Keltschstr. 6a 91058 Erlangen / DE | 06 /
Würstle, Maximilian Lindenstraße 105 91083 Baiersdorf / DE | [2021/11] | Application number, filing date | 19197515.0 | 16.09.2019 | [2021/11] | Filing language | EN | Procedural language | EN | Publication | Type: | A1 Application with search report | No.: | EP3792923 | Date: | 17.03.2021 | Language: | EN | [2021/11] | Search report(s) | (Supplementary) European search report - dispatched on: | EP | 19.02.2020 | Classification | IPC: | G16B50/10, G16H50/70 | [2021/11] | CPC: |
G16B50/10 (EP);
G16B20/20 (CN);
G16H10/60 (US);
G06F21/31 (CN,US);
G06F21/602 (CN);
G06F21/6227 (US);
G16B15/30 (CN);
G16B20/00 (US);
G16B50/30 (US);
G16H50/20 (CN);
G16H50/70 (EP);
G16H70/20 (US);
| 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 [2021/11] | Extension states | BA | Not yet paid | ME | Not yet paid | Validation states | KH | Not yet paid | MA | Not yet paid | MD | Not yet paid | TN | Not yet paid | Title | German: | VERFAHREN UND VORRICHTUNG ZUM AUSTAUSCH VON INFORMATIONEN HINSICHTLICH DER KLINISCHEN IMPLIKATIONEN VON GENOMISCHEN VARIATIONEN | [2021/11] | English: | METHOD AND DEVICE FOR EXCHANGING INFORMATION REGARDING THE CLINICAL IMPLICATIONS OF GENOMIC VARIATIONS | [2021/11] | French: | PROCÉDÉ ET DISPOSITIF D'ÉCHANGER D'INFORMATIONS RELATIVES AUX IMPLICATIONS CLINIQUES DE VARIATIONS GÉNOMIQUES | [2021/11] | Examination procedure | 15.10.2020 | Amendment by applicant (claims and/or description) | 19.10.2020 | Examination requested [2021/11] | 19.10.2020 | Date on which the examining division has become responsible | 09.06.2023 | Despatch of a communication from the examining division (Time limit: M04) | 09.10.2023 | Application withdrawn by applicant [2023/46] | Fees paid | Renewal fee | 17.09.2021 | Renewal fee patent year 03 | 19.09.2022 | Renewal fee patent year 04 |
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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 | [I]US2016048564 (BASSETT JR DOUGLAS E [US], et al) [I] 1-15* paragraphs [0045] - [0189] *; | [I] - Marc Fiume, "System for Interpretation of Personal Genomes", ISBN 978-1-339-35927-4, (20150101), URL: https://tspace.library.utoronto.ca/bitstream/1807/69278/3/Fiume_Marc_201506_PhD_thesis.pdf, XP055494359 [I] 1-15 * pages 70-125 * | [I] - Jeremy L Warner ET AL, "SMART Cancer Navigator: A Framework for Implementing ASCO Workshop Recommendations to Enable Precision Cancer Medicine INTRODUCTION", (20180101), URL: https://ascopubs.org/doi/pdfdirect/10.1200/PO.17.00292, (20200207), XP055666341 [I] 1-15 * the whole document * DOI: http://dx.doi.org/10.1200/PO.17.00292 | [I] - POWELL PATRICK CHENG TAN ET AL, "Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdb", HUMAN MUTATION, US, (20160520), vol. 37, no. 8, doi:10.1002/humu.23011, ISSN 1059-7794, pages 719 - 726, XP055494358 [I] 1-15 * the whole document * DOI: http://dx.doi.org/10.1002/humu.23011 | [I] - LINDA HUANG ET AL, "The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations", JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION, AMSTERDAM, NL, (20161027), doi:10.1093/jamia/ocw148, ISSN 1067-5027, page ocw148, XP055666328 [I] 1-15 * the whole document * DOI: http://dx.doi.org/10.1093/jamia/ocw148 |