MA54538A - Inhibiteurs d'apol1 et leurs procédés d'utilisation - Google Patents
Inhibiteurs d'apol1 et leurs procédés d'utilisationInfo
- Publication number
- MA54538A MA54538A MA054538A MA54538A MA54538A MA 54538 A MA54538 A MA 54538A MA 054538 A MA054538 A MA 054538A MA 54538 A MA54538 A MA 54538A MA 54538 A MA54538 A MA 54538A
- Authority
- MA
- Morocco
- Prior art keywords
- apol1
- inhibitors
- methods
- apol1 inhibitors
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Urology & Nephrology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862780667P | 2018-12-17 | 2018-12-17 | |
| EP19839496.7A EP3897833B1 (fr) | 2018-12-17 | 2019-12-17 | Inhibiteurs d'apol1 et leurs procédés d'utilisation |
| PCT/US2019/066746 WO2020131807A1 (fr) | 2018-12-17 | 2019-12-17 | Inhibiteurs d'apol1 et leurs procédés d'utilisation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA54538A true MA54538A (fr) | 2021-10-27 |
| MA54538B1 MA54538B1 (fr) | 2026-04-30 |
Family
ID=69182627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA54538A MA54538B1 (fr) | 2018-12-17 | 2019-12-17 | Inhibiteurs d'apol1 et leurs procédés d'utilisation |
Country Status (35)
| Country | Link |
|---|---|
| US (3) | US11618746B2 (fr) |
| EP (2) | EP4782443A1 (fr) |
| JP (1) | JP7573528B2 (fr) |
| KR (2) | KR102912203B1 (fr) |
| CN (1) | CN113453760B (fr) |
| AR (1) | AR116913A1 (fr) |
| AU (1) | AU2019405477B2 (fr) |
| CA (1) | CA3121910A1 (fr) |
| CL (1) | CL2021001561A1 (fr) |
| CO (1) | CO2021009053A2 (fr) |
| CR (1) | CR20210383A (fr) |
| DK (1) | DK3897833T3 (fr) |
| DO (1) | DOP2021000116A (fr) |
| EC (1) | ECSP21052184A (fr) |
| ES (1) | ES3067546T3 (fr) |
| FI (1) | FI3897833T3 (fr) |
| HR (1) | HRP20260487T1 (fr) |
| IL (2) | IL319575A (fr) |
| JO (3) | JOP20210131A1 (fr) |
| LT (1) | LT3897833T (fr) |
| MA (1) | MA54538B1 (fr) |
| MD (1) | MD3897833T2 (fr) |
| MX (1) | MX2021007152A (fr) |
| PE (1) | PE20212302A1 (fr) |
| PL (1) | PL3897833T3 (fr) |
| PT (1) | PT3897833T (fr) |
| RS (1) | RS68055B1 (fr) |
| SA (1) | SA521422270B1 (fr) |
| SG (1) | SG11202105769XA (fr) |
| SI (1) | SI3897833T1 (fr) |
| SM (1) | SMT202600169T1 (fr) |
| TW (1) | TWI848031B (fr) |
| UA (1) | UA128375C2 (fr) |
| UY (1) | UY38514A (fr) |
| WO (1) | WO2020131807A1 (fr) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LT3897833T (lt) * | 2018-12-17 | 2026-04-27 | Vertex Pharmaceuticals Incorporated | Apol1 inhibitoriai ir jų panaudojimo būdai |
| EP4097083A1 (fr) * | 2020-01-29 | 2022-12-07 | Vertex Pharmaceuticals Incorporated | Inhibiteurs d'apol1 et leurs méthodes d'utilisation |
| US20210246121A1 (en) * | 2020-02-04 | 2021-08-12 | Vertex Pharmaceuticals Incorporated | Solid forms of apol1 inhibitor and methods of using same |
| EP4114385A1 (fr) | 2020-03-06 | 2023-01-11 | Vertex Pharmaceuticals Incorporated | Méthodes de traitement de la glomérulosclérose segmentaire et focale dépendante de l'apol -1 |
| EP4146633A4 (fr) | 2020-05-07 | 2024-09-25 | Rambam Med-Tech Ltd. | Composition destinée à être utilisée dans le traitement d'une maladie associée à apol1 |
| CN115867543A (zh) * | 2020-06-12 | 2023-03-28 | 弗特克斯药品有限公司 | Apol1抑制剂的固体形式及其使用方法 |
| JP2023530271A (ja) * | 2020-06-12 | 2023-07-14 | バーテックス ファーマシューティカルズ インコーポレイテッド | Apol1の阻害剤及びこれを使用する方法 |
| US20230014907A1 (en) * | 2020-06-12 | 2023-01-19 | Vertex Pharmaceuticals Incorporated | Inhibitors of apol1 and methods of using same |
| BR112023003423A2 (pt) | 2020-08-26 | 2023-03-21 | Vertex Pharma | Inibidores de apol1 e métodos de uso destes |
| CA3179178A1 (fr) | 2021-02-19 | 2022-08-25 | Maze Therapeutics, Inc. | Inhibiteurs d'apol1 et methodes d'utilisation |
| KR20240051990A (ko) * | 2021-08-26 | 2024-04-22 | 버텍스 파마슈티칼스 인코포레이티드 | 스피로트리시클릭 apol1 억제제의 고형분 형태 및 이의 사용 방법 |
| AU2022401847A1 (en) * | 2021-11-30 | 2024-06-06 | Vertex Pharmaceuticals Incorporated | Spirocyclic inhibitors of apol1 and methods of using same |
| US12612379B2 (en) | 2021-11-30 | 2026-04-28 | Vertex Pharmaceuticals Incorporated | Inhibitors of APOL1 and methods of using same |
| MX2024008868A (es) * | 2022-01-18 | 2024-09-23 | Maze Therapeutics Inc | Inhibidores de la apolipoproteína l1 (apol1) y métodos de uso. |
| CN119343353A (zh) * | 2022-02-08 | 2025-01-21 | 弗特克斯药品有限公司 | 作为APOL1抑制剂的2-甲基-4',5'-二氢螺[哌啶-4,7'-噻吩并[2,3-c]吡喃]衍生物和其使用方法 |
| WO2023194895A1 (fr) | 2022-04-06 | 2023-10-12 | Glaxosmithkline Intellectual Property Development Limited | Dérivés pyrroliques utilisés en tant qu'inhibiteurs de l'apolipoprotéine l-1 |
| US20260055083A1 (en) * | 2022-08-19 | 2026-02-26 | Maze Therapeutics, Inc. | Apol1 inhibitors and methods of use |
| WO2025006262A1 (fr) * | 2023-06-29 | 2025-01-02 | Omniab, Inc. | Composés tétracycliques contenant un indole fusionné pour le traitement d'une maladie rénale chronique médiée par apol1 |
| GB202401326D0 (en) * | 2024-02-01 | 2024-03-20 | Podium Bio Ltd | Novel compounds |
| KR20250122547A (ko) | 2024-02-05 | 2025-08-14 | 서주사이언티픽 주식회사 | AIoT 기반 방사성 동위원소 관리 시스템 |
| TW202613098A (zh) * | 2024-07-09 | 2026-04-01 | 大陸商上海旭成醫藥科技有限公司 | 一種APOLs抑制劑 |
Family Cites Families (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4039676A (en) | 1975-06-23 | 1977-08-02 | Ciba-Geigy Corporation | 2-piperidinoalkyl-1,4-benzodioxans |
| CA2262569A1 (fr) | 1996-08-09 | 1998-02-19 | Norihito Ohi | Derives de benzopiperidine |
| EP0924209B1 (fr) | 1997-12-19 | 2003-05-02 | Eli Lilly And Company | Imidazolines hypoglycémiques |
| GB9905010D0 (en) | 1999-03-04 | 1999-04-28 | Merck Sharp & Dohme | Therapeutic agents |
| WO2001017965A2 (fr) | 1999-09-07 | 2001-03-15 | Syngenta Participations Ag | Cyanopiperidines |
| FR2801585B1 (fr) | 1999-11-25 | 2002-02-15 | Fournier Ind & Sante | Nouveaux antagonistes des recepteurs de l'ii-8 |
| GB0003397D0 (en) | 2000-02-14 | 2000-04-05 | Merck Sharp & Dohme | Therapeutic agents |
| WO2002028831A1 (fr) | 2000-10-02 | 2002-04-11 | Merck & Co., Inc. | Inhibiteurs de la prenyl-proteine transferase |
| FR2824826B1 (fr) | 2001-05-17 | 2003-11-07 | Fournier Lab Sa | Nouveaux derives de 5-cyano-1h-indole antagonistes des recepteurs de l'interleukine-8 |
| FR2824827B1 (fr) | 2001-05-17 | 2004-02-13 | Fournier Lab Sa | Nouveaux derives de 5-phenyl-1h-indole antagoniste des recepteurs de l'interleukine-8 |
| KR20050044450A (ko) | 2001-11-14 | 2005-05-12 | 테바 파마슈티컬 인더스트리즈 리미티드 | 로사르탄 칼륨의 무정형 및 결정형 형태 및 이의 제조 방법 |
| WO2003104180A1 (fr) * | 2002-06-05 | 2003-12-18 | Natco Pharma Limited | Procede de preparation d'acide 4-(4-fluorobenzoyl) butyrique |
| WO2004058717A1 (fr) | 2002-12-20 | 2004-07-15 | X-Ceptor Therapeutics, Inc. | Derives d'isoquinolinone et leur utilisation comme agents therapeutiques |
| AU2004268919A1 (en) | 2003-09-03 | 2005-03-10 | Galapagos Nv | Novel 4-piperidinecarboxamide and the use thereof for the preparation of medicaments against 5-HT2A receptor-related disorders |
| WO2005092854A1 (fr) | 2004-03-03 | 2005-10-06 | Eli Lilly And Company | Modulateurs de recepteur nucleaire d'hormones steroides a base de derives indole substitues bicycliques |
| AR048523A1 (es) | 2004-04-07 | 2006-05-03 | Kalypsys Inc | Compuestos con estructura de aril sulfonamida y sulfonilo como moduladores de ppar y metodos para tratar trastornos metabolicos |
| WO2007061763A2 (fr) | 2005-11-22 | 2007-05-31 | Merck & Co., Inc. | Antagonistes des recepteurs de l’indole orexine |
| US8222288B2 (en) | 2006-08-30 | 2012-07-17 | The Regents Of The University Of Michigan | Small molecule inhibitors of MDM2 and the uses thereof |
| EP2086935A1 (fr) | 2006-10-16 | 2009-08-12 | Grünenthal GmbH | Derives de sulfonamide substitues en tant que modulateurs du recepteur de bradykinine-1 |
| CN101563324A (zh) | 2006-12-22 | 2009-10-21 | 弗·哈夫曼-拉罗切有限公司 | 螺-哌啶衍生物 |
| PT2118074E (pt) * | 2007-02-01 | 2014-03-20 | Resverlogix Corp | Compostos para a prevenção e tratamento de doenças cardiovasculares |
| EP2020414A1 (fr) | 2007-06-20 | 2009-02-04 | Laboratorios del Dr. Esteve S.A. | Derivés spiro[piperidine-4,4'-thieno[3,2-c]pyran] et composés similaires en tant que inhibiteurs du recepteur sigma pour le traitement de pyschose |
| EP2178870B1 (fr) | 2007-08-17 | 2018-09-19 | LG Chem, Ltd. | Composés d'indole et d'indazole en tant qu'inhibiteurs de nécrose cellulaire |
| KR101605061B1 (ko) | 2009-05-29 | 2016-03-21 | 라퀄리아 파마 인코포레이티드 | 칼슘 또는 나트륨 채널 차단제로서의 아릴 치환된 카복사미드 유도체 |
| UA107943C2 (xx) | 2009-11-16 | 2015-03-10 | Lilly Co Eli | Сполуки спіропіперидину як антагоністи рецептора orl-1 |
| PL2501704T3 (pl) | 2009-11-16 | 2014-02-28 | Lilly Co Eli | Spiropiperydynowe związki jako antagoniści receptora ORL-1 |
| WO2012025155A1 (fr) | 2010-08-26 | 2012-03-01 | Novartis Ag | Composés à base d'hydroxamate en tant qu'inhibiteurs des désacétylases |
| BR102012024778A2 (pt) | 2012-09-28 | 2014-08-19 | Cristalia Prod Quimicos Farm | Compostos heteroaromáticos; processo para preparar os compostos, composições farmacêuticas, usos e método de tratamento para as dores aguda e crônica |
| US10130632B2 (en) | 2012-11-27 | 2018-11-20 | Beth Israel Deaconess Medical Center, Inc. | Methods for treating renal disease |
| US9850203B2 (en) * | 2013-09-26 | 2017-12-26 | Pharmakea, Inc. | Autotaxin inhibitor compounds |
| ES2895490T3 (es) | 2014-03-27 | 2022-02-21 | Acad Medisch Ct | Iminoazúcares N-(5-(bifen-4-ilmetiloxi)pentil)-sustituidos como inhibidores de glucosilceramida sintasa |
| WO2016029310A1 (fr) | 2014-08-27 | 2016-03-03 | The Governing Council Of The University Of Toronto | Modulateurs du récepteur cannabinoïde de type 1 |
| BR112017007178A2 (pt) | 2014-10-08 | 2017-12-19 | Ass Francaise Contre Les Myopathies | compostos de aminopiridina úteis como inibidores de prenilação de proteína |
| JP2017535545A (ja) | 2014-11-21 | 2017-11-30 | ラボラトリオス・デル・デエレ・エステベ・エセ・ア | 疼痛に対する多様な活性を有するスピロ−イソキノリン−1,4’−ピペリジン化合物 |
| HRP20210472T1 (hr) | 2015-08-27 | 2021-05-14 | Pfizer Inc. | Biciklički kondenzirani heteroarilni ili arilni spojevi kao modulatori irak4 |
| CN108884096B (zh) | 2016-02-08 | 2022-03-22 | 豪夫迈·罗氏有限公司 | 作为ddr1抑制剂的螺二氢吲哚酮 |
| EP3787669A4 (fr) | 2018-04-30 | 2022-03-30 | The Trustees of Indiana University | Composés destinés à moduler les niveaux de ddah et d'adma, ainsi que leurs méthodes d'utilisation pour traiter une maladie |
| CN118127019A (zh) | 2018-05-22 | 2024-06-04 | Ionis制药公司 | Apol1表达的调节剂 |
| LT3897833T (lt) | 2018-12-17 | 2026-04-27 | Vertex Pharmaceuticals Incorporated | Apol1 inhibitoriai ir jų panaudojimo būdai |
| US20220144838A1 (en) | 2019-03-13 | 2022-05-12 | Nanjing Immunophage Biotech Co., Ltd. | Compounds as Inhibitors of Macrophage Migration Inhibitory Factor |
| US12698266B2 (en) | 2019-12-19 | 2026-08-04 | Casma Therapeutics, Inc. | TRPML modulators |
| EP4097083A1 (fr) | 2020-01-29 | 2022-12-07 | Vertex Pharmaceuticals Incorporated | Inhibiteurs d'apol1 et leurs méthodes d'utilisation |
| US20210246121A1 (en) * | 2020-02-04 | 2021-08-12 | Vertex Pharmaceuticals Incorporated | Solid forms of apol1 inhibitor and methods of using same |
| EP4114385A1 (fr) * | 2020-03-06 | 2023-01-11 | Vertex Pharmaceuticals Incorporated | Méthodes de traitement de la glomérulosclérose segmentaire et focale dépendante de l'apol -1 |
| CA3171950A1 (fr) | 2020-04-22 | 2021-10-28 | David William Sheppard | Inhibiteurs de traduction de collagene 1 et leurs procedes d'utilisation |
| HUP2200468A1 (hu) | 2020-04-29 | 2023-03-28 | X Chem Zrt | IAP antagonisták és gyógyászati alkalmazásuk |
| EP4146633A4 (fr) | 2020-05-07 | 2024-09-25 | Rambam Med-Tech Ltd. | Composition destinée à être utilisée dans le traitement d'une maladie associée à apol1 |
| JP2023530271A (ja) | 2020-06-12 | 2023-07-14 | バーテックス ファーマシューティカルズ インコーポレイテッド | Apol1の阻害剤及びこれを使用する方法 |
| CN115867543A (zh) | 2020-06-12 | 2023-03-28 | 弗特克斯药品有限公司 | Apol1抑制剂的固体形式及其使用方法 |
| US20230014907A1 (en) | 2020-06-12 | 2023-01-19 | Vertex Pharmaceuticals Incorporated | Inhibitors of apol1 and methods of using same |
| BR112023003423A2 (pt) | 2020-08-26 | 2023-03-21 | Vertex Pharma | Inibidores de apol1 e métodos de uso destes |
| KR20240051990A (ko) | 2021-08-26 | 2024-04-22 | 버텍스 파마슈티칼스 인코포레이티드 | 스피로트리시클릭 apol1 억제제의 고형분 형태 및 이의 사용 방법 |
| US12612379B2 (en) | 2021-11-30 | 2026-04-28 | Vertex Pharmaceuticals Incorporated | Inhibitors of APOL1 and methods of using same |
| AU2022401847A1 (en) | 2021-11-30 | 2024-06-06 | Vertex Pharmaceuticals Incorporated | Spirocyclic inhibitors of apol1 and methods of using same |
| CN119343353A (zh) | 2022-02-08 | 2025-01-21 | 弗特克斯药品有限公司 | 作为APOL1抑制剂的2-甲基-4',5'-二氢螺[哌啶-4,7'-噻吩并[2,3-c]吡喃]衍生物和其使用方法 |
| WO2023154314A1 (fr) | 2022-02-08 | 2023-08-17 | Vertex Pharmaceuticals Incorporated | Dérivés de spiro pipéridine utilisés en tant qu'inhibiteurs de apol1 et leurs procédés d'utilisation |
| EP4476199A1 (fr) | 2022-02-08 | 2024-12-18 | Vertex Pharmaceuticals Incorporated | Dérivés de 2-méthyl-4-phénylpipéridin-4-ol utilisés en tant qu'inhibiteurs de apol1 et leurs procédés d'utilisation |
| EP4476228A1 (fr) | 2022-02-08 | 2024-12-18 | Vertex Pharmaceuticals Incorporated | Dérivés de 4',5'-dihydrospiro[pipéridine-4,7'-thiéno[2,3-c]pyran] utilisés en tant qu'inhibiteurs de apol1 et leurs procédés d'utilisation |
-
2019
- 2019-12-17 LT LTEPPCT/US2019/066746T patent/LT3897833T/lt unknown
- 2019-12-17 CR CR20210383A patent/CR20210383A/es unknown
- 2019-12-17 EP EP26155786.2A patent/EP4782443A1/fr active Pending
- 2019-12-17 IL IL319575A patent/IL319575A/en unknown
- 2019-12-17 SM SM20260169T patent/SMT202600169T1/it unknown
- 2019-12-17 MD MDE20211053T patent/MD3897833T2/en unknown
- 2019-12-17 JO JOP/2021/0131A patent/JOP20210131A1/ar unknown
- 2019-12-17 UY UY0001038514A patent/UY38514A/es active IP Right Grant
- 2019-12-17 AR ARP190103717A patent/AR116913A1/es unknown
- 2019-12-17 UA UAA202104153A patent/UA128375C2/uk unknown
- 2019-12-17 EP EP19839496.7A patent/EP3897833B1/fr active Active
- 2019-12-17 HR HRP20260487TT patent/HRP20260487T1/hr unknown
- 2019-12-17 SG SG11202105769XA patent/SG11202105769XA/en unknown
- 2019-12-17 MX MX2021007152A patent/MX2021007152A/es unknown
- 2019-12-17 RS RS20260459A patent/RS68055B1/sr unknown
- 2019-12-17 TW TW108146307A patent/TWI848031B/zh active
- 2019-12-17 PL PL19839496.7T patent/PL3897833T3/pl unknown
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2021
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2023
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2024
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