EP3661523 - METHODS OF TREATING GENETIC HEARING LOSS [Right-click to bookmark this link] | Status | Examination is in progress Status updated on 29.08.2024 Database last updated on 03.09.2024 | |
Former | Request for examination was made Status updated on 08.05.2020 | ||
Former | The international publication has been made Status updated on 09.02.2019 | Most recent event Tooltip | 30.08.2024 | First examination report | Applicant(s) | For all designated states University of Iowa Research Foundation 2660 University Capitol Centre Iowa City, IA 52242 / US | [2020/24] | Inventor(s) | 01 /
SMITH, Richard, J. 112 N. Capitol Street 6 Gilmore Hall Iowa City Iowa 52242-5500 / US | 02 /
RANUM, Paul, T. 112 N. Capitol Street 6 Gilmore Hall Iowa City Iowa 52242-5500 / US | [2020/24] | Representative(s) | PATERIS Patentanwälte PartmbB Postfach 33 07 11 80067 München / DE | [N/P] |
Former [2020/24] | PATERIS Patentanwälte PartmbB Altheimer Eck 13 80331 München / DE | Application number, filing date | 18842414.7 | 02.08.2018 | [2020/24] | WO2018US44996 | Priority number, date | US201762540890P | 03.08.2017 Original published format: US 201762540890 P | [2020/24] | Filing language | EN | Procedural language | EN | Publication | Type: | A2 Application without search report | No.: | WO2019028246 | Date: | 07.02.2019 | Language: | EN | [2019/06] | Type: | A2 Application without search report | No.: | EP3661523 | Date: | 10.06.2020 | Language: | EN | The application published by WIPO in one of the EPO official languages on 07.02.2019 takes the place of the publication of the European patent application. | [2020/24] | Search report(s) | International search report - published on: | US | 28.02.2019 | (Supplementary) European search report - dispatched on: | EP | 01.07.2021 | Classification | IPC: | C12N15/113, A61P27/16, A61K48/00, A61K31/713, A61K35/76, A61K31/7105, A61K45/06 | [2021/17] | CPC: |
C12N15/113 (EP);
C12N15/86 (US);
A61K31/7105 (EP);
A61K31/713 (EP);
A61K45/06 (EP);
A61K48/005 (EP);
A61K48/0066 (US);
G01N33/6893 (US);
A01K2227/105 (EP);
A61K9/0019 (US);
C12N2310/14 (EP);
C12N2310/141 (EP,US);
C12N2310/20 (US);
C12N2320/31 (EP);
C12N2750/14142 (EP);
C12N2750/14143 (EP)
(-)
| C-Set: |
A61K31/7105, A61K2300/00 (EP);
A61K31/713, A61K2300/00 (EP) |
Former IPC [2020/24] | A61K31/7088, A61K31/7105, A61P27/16, C12N15/09, C12N15/113, C12N15/63, C12N15/85, C12N15/86, C12N15/861 | 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 [2020/24] | Title | German: | VERFAHREN ZUR BEHANDLUNG VON GENETISCHEM HÖRVERLUST | [2020/24] | English: | METHODS OF TREATING GENETIC HEARING LOSS | [2020/24] | French: | MÉTHODES DE TRAITEMENT DE LA PERTE AUDITIVE GÉNÉTIQUE | [2020/24] | Entry into regional phase | 27.02.2020 | National basic fee paid | 27.02.2020 | Search fee paid | 27.02.2020 | Designation fee(s) paid | 27.02.2020 | Examination fee paid | Examination procedure | 27.02.2020 | Examination requested [2020/24] | 22.02.2022 | Despatch of communication that the application is deemed to be withdrawn, reason: reply to the Extended European Search Report/Written Opinion of the International Searching Authority/International Preliminary Examination Report/Supplementary international search report not received in time | 03.05.2022 | Amendment by applicant (claims and/or description) | 28.08.2024 | Despatch of a communication from the examining division (Time limit: M04) | Request for further processing for: | The application is deemed to be withdrawn due to failure to reply to the Extended European Search Report/Written Opinion of the International Searching Authority/International Preliminary Examination Report/Supplementary international search report/Supplementary European search report | 03.05.2022 | Request for further processing filed | 03.05.2022 | Full payment received (date of receipt of payment) Request granted | 16.05.2022 | Decision despatched | Fees paid | Renewal fee | 27.08.2020 | Renewal fee patent year 03 | 27.08.2021 | Renewal fee patent year 04 | 29.08.2022 | Renewal fee patent year 05 | 28.08.2023 | Renewal fee patent year 06 | 27.08.2024 | Renewal fee patent year 07 |
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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]WO2008125846 (TRINITY COLLEGE DUBLIN [IE], et al); | [A]WO2010029303 (ISIS INNOVATION [GB], et al); | [A]WO2016016449 (ASS INST DE MYOLOGIE [FR], et al); | [I]US2016090597 (SMITH RICHARD J H [US], et al); | [X]WO2016176690 (UNIV COLUMBIA [US]); | [I]WO2017100791 (MASSACHUSETTS EYE & EAR INFIRMARY [US], et al); | International search | [A]US2004249139 (GRIFFITH ANDREW J [US], et al) [A] 1-4, 5/1-4, 6/1-4 * ; abstract; paragraphs [0019], [0034] *; | [XY]US2016090597 (SMITH RICHARD J H [US], et al) [X] 24-27 * ; abstract; paragraphs [0007], [0008], [0012], [0013], [0024], [0028], [0186], [0187] * [Y] 8-9, 10/8-9, 11/8-9, 28/24-27, 33-34; | [Y] - SCHRAUWEN, I et al., "A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment", American Journal of Human Genetics, (20120913), vol. 91, no. 4, doi:doi:10.1016/j.ajhg.2012.08.018, pages 636 - 645, XP055562747 [Y] 8-9, 10/8-9, 11/8-9, 34 * ; abstract; page 636, 1st column, 1st paragraph; page 638, 1st column, 5th paragraph; DOI: 10.1016/j.ajhg.2012.08.018 * DOI: http://dx.doi.org/10.1016/j.ajhg.2012.08.018 | [Y] - SANDS, MS et al., "Percutaneous Intravenous Injection in Neonatal Mice", Laboratory Animal Science, (19990600), vol. 49, no. 3, pages 328 - 330, XP055580394 [Y] 28/24-27, 33 * ; page 328, 2nd column, 3rd paragraph * | [Y] - SHEARER, AE et al., "Comprehensive gonetic testing for hereditary hearing loss using massively parallel sequencing", Proceedings of the National Academy of Sciences of the U.S.A., (20101115), vol. 107, no. 49, pages 21104 - 21109, XP055580396 [Y] 34 * ; page 21108, 1st column, 3rd to 5th paragraphs; Table 2; DOI: 10.1073/pnas.1012989107 * DOI: http://dx.doi.org/10.1073/pnas.1012989107 | [A] - TSHIBATA, SB et al., "RNA Interference Prevents Autosomal-Dominant Hearing Loss", American Journal of Human Genetics, (20160526), vol. 98, no. 6, doi:doi:10.1016/j.ajhg.2016.03.028, pages 1101 - 1113, XP029567269 [A] 1-4, 5/1-4, 6/1-4 * ; abstract; page 1101, 2nd column, 1st paragraph; page 1104, 2nd column, 4th paragraph; page 1105, 1st column, 1st paragraph; Figure 1D: DOI: 10.1016/j.ajhg.2016.03.028 * DOI: http://dx.doi.org/10.1016/j.ajhg.2016.03.028 |