MA44721B1 - Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer - Google Patents
Inhibiteurs de mcl1 macrocycliques pour le traitement du cancerInfo
- Publication number
- MA44721B1 MA44721B1 MA44721A MA44721A MA44721B1 MA 44721 B1 MA44721 B1 MA 44721B1 MA 44721 A MA44721 A MA 44721A MA 44721 A MA44721 A MA 44721A MA 44721 B1 MA44721 B1 MA 44721B1
- Authority
- MA
- Morocco
- Prior art keywords
- macrocyclic
- cancer treatment
- acid
- mcl1 inhibitors
- pentaazaheptacyclo
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- 102100026539 Induced myeloid leukemia cell differentiation protein Mcl-1 Human genes 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 101150094281 mcl1 gene Proteins 0.000 title 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D497/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D497/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
L'invention concerne un composé qui est l'acide 17-chloro-5,13,14,22-tétraméthyl-28-oxa-2,9-dithia-5,6,12,13,22-pentaazaheptacyclo[27.7.1.14,7.011,15.016,21.020,24.030,35]octatriaconta-1(37),4(38),6,11,14,16,18,20,23,29,31,33,35-tridécaène-23-carboxylique (formule 1), des énantiomères et des sels pharmaceutiquement acceptables correspondants. L'invention concerne également des compositions pharmaceutiques de l'acide 17-chloro-5,13,14,22-tétraméthyl-28-oxa-2,9-dithia-5,6,12,13,22-pentaazaheptacyclo[27.7.1.14,7.011,15.016,21.020,24.030,35]octatriaconta-1(37),4(38),6,11,14,16,18,20,23,29,31,33,35-tridécaène-23-carboxylique, et des énantiomères et des sels pharmaceutiquement acceptables correspondants, et des méthodes de traitement du cancer avec ces composés et ces compositions.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662326156P | 2016-04-22 | 2016-04-22 | |
| PCT/EP2017/059511 WO2017182625A1 (fr) | 2016-04-22 | 2017-04-21 | Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA44721A MA44721A (fr) | 2019-02-27 |
| MA44721B1 true MA44721B1 (fr) | 2020-05-29 |
Family
ID=58664658
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA44721A MA44721B1 (fr) | 2016-04-22 | 2017-04-21 | Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer |
Country Status (37)
| Country | Link |
|---|---|
| US (4) | US9840518B2 (fr) |
| EP (1) | EP3445767B1 (fr) |
| JP (1) | JP6894449B2 (fr) |
| KR (1) | KR102388208B1 (fr) |
| CN (1) | CN109071566B (fr) |
| AR (1) | AR108301A1 (fr) |
| AU (1) | AU2017252222B2 (fr) |
| BR (1) | BR112018070677B1 (fr) |
| CL (1) | CL2018002410A1 (fr) |
| CO (1) | CO2018008759A2 (fr) |
| CR (1) | CR20180499A (fr) |
| CY (1) | CY1123186T1 (fr) |
| DK (1) | DK3445767T3 (fr) |
| DO (1) | DOP2018000222A (fr) |
| EA (1) | EA036551B1 (fr) |
| ES (1) | ES2791319T3 (fr) |
| HR (1) | HRP20200673T1 (fr) |
| HU (1) | HUE049591T2 (fr) |
| IL (1) | IL262237B (fr) |
| LT (1) | LT3445767T (fr) |
| MA (1) | MA44721B1 (fr) |
| ME (1) | ME03729B (fr) |
| MX (1) | MX386103B (fr) |
| NI (1) | NI201800093A (fr) |
| PE (1) | PE20181803A1 (fr) |
| PH (1) | PH12018502227A1 (fr) |
| PL (1) | PL3445767T3 (fr) |
| PT (1) | PT3445767T (fr) |
| RS (1) | RS60257B1 (fr) |
| SG (1) | SG11201805838UA (fr) |
| SI (1) | SI3445767T1 (fr) |
| SM (1) | SMT202000249T1 (fr) |
| SV (1) | SV2018005742A (fr) |
| TN (1) | TN2018000319A1 (fr) |
| TW (1) | TWI742074B (fr) |
| WO (1) | WO2017182625A1 (fr) |
| ZA (1) | ZA201807766B (fr) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108697729B (zh) | 2016-02-04 | 2023-05-09 | 约翰霍普金斯大学 | 新型GLUT抑制剂rapaglutin及其用途 |
| US11066416B2 (en) | 2016-02-04 | 2021-07-20 | The Johns Hopkins University | Rapafucin derivative compounds and methods of use thereof |
| AU2017214557B2 (en) | 2016-02-04 | 2022-05-19 | The Johns Hopkins University | Rapadocins, inhibitors of equilibrative nucleoside transporter 1 and uses thereof |
| CR20180499A (es) | 2016-04-22 | 2019-01-25 | Astrazeneca Ab | Inhibidores de mcl1 macrocicliclos para tratar el cancer |
| EP3458459B1 (fr) | 2016-05-19 | 2022-04-27 | Bayer Aktiengesellschaft | Derivés d'indole macrocycliques |
| TW201904976A (zh) * | 2017-03-31 | 2019-02-01 | 瑞典商阿斯特捷利康公司 | Ｍｃｌ-１抑制劑及其使用方法 |
| TWI781996B (zh) * | 2017-03-31 | 2022-11-01 | 瑞典商阿斯特捷利康公司 | 合成ｍｃｌ-１抑制劑之方法 |
| AU2018317828A1 (en) * | 2017-08-15 | 2020-04-02 | AbbVie Deutschland GmbH & Co. KG | Macrocyclic MCL-1 inhibitors and methods of use |
| CR20200124A (es) | 2017-08-15 | 2020-09-28 | Abbvie Inc | Inhibidores macrocíclicos de mcl-1 y métodos de uso |
| AR113887A1 (es) * | 2017-11-17 | 2020-06-24 | Bayer Ag | Derivados de indol macrocíclicos sustituidos con cloro |
| EP3710456B1 (fr) | 2017-11-17 | 2022-09-21 | The Broad Institute, Inc. | Dérivés d'indole macrocycliques |
| EP3710449B1 (fr) | 2017-11-17 | 2022-07-06 | The Broad Institute, Inc. | Dérivés d'indole macrocycliques substitués par du fluor utilisés en tant qu'inhibiteurs de mcl-1, destinés à être utilisés dans le traitement du cancer |
| EP3710451A1 (fr) * | 2017-11-17 | 2020-09-23 | Bayer Aktiengesellschaft | Dérivés d'indole macrocycliques substitués |
| WO2019096914A1 (fr) * | 2017-11-17 | 2019-05-23 | Bayer Aktiengesellschaft | Dérivés d'indole macrocycliques substitués par du chlore |
| WO2019096907A1 (fr) * | 2017-11-17 | 2019-05-23 | Bayer Aktiengesellschaft | Dérivés d'indole macrocycliques annelés aryle |
| TW202014184A (zh) * | 2018-04-30 | 2020-04-16 | 瑞典商阿斯特捷利康公司 | 用於治療癌症之組合 |
| WO2020063792A1 (fr) * | 2018-09-30 | 2020-04-02 | 江苏恒瑞医药股份有限公司 | Dérivé macrocyclique d'indole, son procédé de préparation et son application en médecine |
| TWI810397B (zh) | 2018-11-14 | 2023-08-01 | 瑞典商阿斯特捷利康公司 | 治療癌症之方法 |
| CN111205309B (zh) * | 2018-11-21 | 2023-04-07 | 江苏恒瑞医药股份有限公司 | 吲哚类大环衍生物、其制备方法及其在医药上的应用 |
| TWI749404B (zh) * | 2018-11-22 | 2021-12-11 | 大陸商蘇州亞盛藥業有限公司 | 作為mcl-1抑制劑的大環吲哚 |
| WO2020151738A1 (fr) * | 2019-01-23 | 2020-07-30 | Ascentage Pharma (Suzhou) Co., Ltd. | Pyrrazoles fusionnés macrocycliques utilisés en tant qu'inhibiteurs de mcl-1 |
| CA3131939A1 (fr) * | 2019-03-08 | 2020-09-17 | Zeno Management, Inc. | Composes macrocycliques |
| KR20210151183A (ko) | 2019-04-11 | 2021-12-13 | 브리스톨-마이어스 스큅 컴퍼니 | 치료 혈장 농도를 달성하기 위한 무정형 고체 및 가용화된 제제의 증진된 성능 |
| WO2020221272A1 (fr) * | 2019-04-30 | 2020-11-05 | 江苏恒瑞医药股份有限公司 | Dérivé macrocyclique d'indole, son procédé de préparation et son utilisation en médecine |
| ES3075769T3 (en) | 2019-05-10 | 2026-08-07 | Janssen Biotech Inc | Macrocyclic chelators and methods of use thereof |
| EP3969457B1 (fr) | 2019-05-17 | 2025-08-13 | The Broad Institute Inc. | Procédés de préparation d'indoles macrocycliques |
| AU2020279979A1 (en) | 2019-05-20 | 2021-11-25 | Les Laboratoires Servier | Mcl-1 inhibitor antibody-drug conjugates and methods of use |
| MA56505A (fr) | 2019-06-21 | 2022-04-27 | Janssen Pharmaceutica Nv | Inhibiteurs macrocycliques de mcl-1 |
| KR20220034136A (ko) | 2019-07-09 | 2022-03-17 | 얀센 파마슈티카 엔.브이. | Mcl-1 억제제로서의 거대환식 스피로사이클 유도체 |
| WO2021067405A1 (fr) * | 2019-10-01 | 2021-04-08 | The Johns Hopkins University | Composés neuroprotecteurs et leurs procédés d'utilisation |
| WO2021092053A1 (fr) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Composés macrocycliques inhibiteurs de mcl-1 destinés à être utilisées dans la gestion clinique d'états pathologiques provoqués ou induits par des cellules sénescentes ainsi que dans le traitement du cancer |
| WO2021092061A1 (fr) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Polythérapie pour le traitement de maladies associées à la sénescence |
| CA3157590A1 (fr) | 2019-11-21 | 2021-05-27 | Janssen Pharmaceutica Nv | Derives de sulfonyle macrocycliques utilises en tant qu'inhibiteurs de mcl-1 |
| US20230021562A1 (en) | 2019-11-21 | 2023-01-26 | Janssen Pharmaceutica Nv | Macrocylic indole derivatives mcl-1 inhibitors |
| AU2020409006A1 (en) * | 2019-12-18 | 2022-06-30 | Zeno Management, Inc. | Macrocyclic compounds |
| CN115151551B (zh) | 2020-02-21 | 2024-10-25 | 詹森药业有限公司 | 作为mcl-1抑制剂的大环吲哚衍生物 |
| CN115335384B (zh) * | 2020-03-30 | 2024-10-22 | 江苏恒瑞医药股份有限公司 | 一种吲哚类大环衍生物的结晶形式及其制备方法 |
| EP4157852A1 (fr) | 2020-05-29 | 2023-04-05 | JANSSEN Pharmaceutica NV | Dérivés macrocycliques de 7-pyrazol-5-yl-indole utilisés en tant qu'inhibiteurs de mcl-1 |
| CN115943147A (zh) | 2020-06-19 | 2023-04-07 | 詹森药业有限公司 | N-连接的大环7-(吡唑-5-基)-吲哚衍生物作为mcl-1抑制剂 |
| CA3181816A1 (fr) | 2020-06-19 | 2021-12-23 | Aldo Peschiulli | Derives de 4-(pyrazol-5-yl)-indole macrocycliques a liaison n utiles en tant qu'inhibiteurs de mcl-1 |
| CA3184877A1 (fr) | 2020-07-08 | 2022-01-13 | Benoit Christian Albert Ghislain De Boeck | Derives d'indole contenant un ether macrocyclique en tant qu'inhibiteurs de mcl-1 |
| WO2022032284A1 (fr) * | 2020-08-07 | 2022-02-10 | Zeno Management, Inc. | Composés macrocycliques |
| JP2023553808A (ja) | 2020-11-24 | 2023-12-26 | ノバルティス アーゲー | Ｍｃｌ－１阻害剤抗体－薬物コンジュゲートおよび使用方法 |
| WO2022129333A1 (fr) | 2020-12-17 | 2022-06-23 | Janssen Pharmaceutica Nv | Dérivés de 4-(pyrazol-5-yl)-indole macrocycliques ramifiés utilisés en tant qu'inhibiteurs de mcl-1 |
| CN116848126A (zh) | 2021-02-12 | 2023-10-03 | 詹森药业有限公司 | 大环1,3-桥联的6-氯-7-吡唑-4-基-1h-吲哚-2-羧酸酯和6-氯-7-嘧啶-5-基-1h-吲哚-2-羧酸酯衍生物作为mcl-1抑制剂用于治疗癌症 |
| WO2022251247A1 (fr) * | 2021-05-28 | 2022-12-01 | Zeno Management, Inc. | Composés macrocycliques |
| JP7900421B2 (ja) | 2021-06-11 | 2026-08-04 | ギリアード サイエンシーズ， インコーポレイテッド | Ｍｃｌ－１阻害剤と抗がん剤との組み合わせ |
| TWI861509B (zh) | 2021-06-11 | 2024-11-11 | 美商基利科學股份有限公司 | Mcl-1抑制劑與抗體藥物接合物之組合 |
| CN115490708B (zh) * | 2021-06-18 | 2025-01-24 | 苏州亚盛药业有限公司 | 磺酰胺类大环衍生物及其制备方法和用途 |
| US20240401146A1 (en) | 2021-10-06 | 2024-12-05 | Institut National de la Santé et de la Recherche Médicale | Methods for predicting and improving the efficacy of mcl-1 inhibitor therapy |
| IL317101A (en) | 2022-05-20 | 2025-01-01 | Novartis Ag | Antibody-drug conjugates of anticancer compounds and methods of using them |
| UY40985A (es) | 2023-11-22 | 2025-06-30 | Servier Lab | Conjugados de anticuerpo anti-cd74-fármaco y métodos de uso de los mismos |
| AR134424A1 (es) | 2023-11-22 | 2026-01-14 | Novartis Ag | Conjugados de anticuerpo anti-cd7-fármaco y métodos de uso de los mismos |
| TW202530255A (zh) | 2023-12-15 | 2025-08-01 | 法商亞維西亞有限公司 | 抗ｉｌ－１ｒａｐ結合結構域及其抗體－藥物偶聯物 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101511074B1 (ko) * | 2007-04-16 | 2015-04-13 | 애브비 인코포레이티드 | 7-치환된 인돌 Ｍｃｌ-1 억제제 |
| MX2009011210A (es) | 2007-04-16 | 2009-10-30 | Abbott Lab | Inhibidores de mcl1 de indol 7-no sustituido. |
| NZ594019A (en) * | 2008-12-22 | 2013-08-30 | Cubist Pharm Inc | Novel antibacterial agents for the treatment of gram positive infections |
| CN102822163B (zh) * | 2009-12-23 | 2016-01-20 | 艾恩伍德医药品股份有限公司 | Crth2调节剂 |
| AU2012257513B2 (en) * | 2011-05-19 | 2017-05-11 | Fundación Del Sector Público Estatal Centro Nacional De Investigaciones Oncológicas Carlos III (F.S.P. CNIO) | Macrocyclic compounds as protein kinase inhibitors |
| US10093640B2 (en) | 2012-09-21 | 2018-10-09 | Vanderbilt University | Substituted benzofuran, benzothiophene and indole MCL-1 inhibitors |
| WO2015031608A1 (fr) | 2013-08-28 | 2015-03-05 | Vanderbilt University | Inhibiteurs de mcl-1 de type indole substitué |
| WO2015123230A1 (fr) * | 2014-02-12 | 2015-08-20 | Bristol-Myers Squibb Company | Utilisation de macrocycles de benzothiazole comme qu'inhibiteurs de la réplication du virus de l'immunodéficience humaine |
| US10533010B2 (en) | 2014-03-27 | 2020-01-14 | Vanderbilt University | Substituted indole Mcl-1 inhibitors |
| US9963464B2 (en) * | 2014-04-11 | 2018-05-08 | Bayer Pharma Aktiengesellschaft | Macrocyclic compounds |
| US9949965B2 (en) | 2014-10-17 | 2018-04-24 | Vanderbilt University | Tricyclic indole Mcl-1 inhibitors and uses thereof |
| CR20180499A (es) | 2016-04-22 | 2019-01-25 | Astrazeneca Ab | Inhibidores de mcl1 macrocicliclos para tratar el cancer |
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2017
- 2017-04-21 CR CR20180499A patent/CR20180499A/es unknown
- 2017-04-21 EP EP17720720.6A patent/EP3445767B1/fr active Active
- 2017-04-21 ME MEP-2020-99A patent/ME03729B/fr unknown
- 2017-04-21 US US15/493,210 patent/US9840518B2/en active Active
- 2017-04-21 HU HUE17720720A patent/HUE049591T2/hu unknown
- 2017-04-21 SG SG11201805838UA patent/SG11201805838UA/en unknown
- 2017-04-21 LT LTEP17720720.6T patent/LT3445767T/lt unknown
- 2017-04-21 CN CN201780022366.0A patent/CN109071566B/zh active Active
- 2017-04-21 CO CONC2018/0008759A patent/CO2018008759A2/es unknown
- 2017-04-21 TN TNP/2018/000319A patent/TN2018000319A1/en unknown
- 2017-04-21 WO PCT/EP2017/059511 patent/WO2017182625A1/fr not_active Ceased
- 2017-04-21 PL PL17720720T patent/PL3445767T3/pl unknown
- 2017-04-21 DK DK17720720.6T patent/DK3445767T3/da active
- 2017-04-21 HR HRP20200673TT patent/HRP20200673T1/hr unknown
- 2017-04-21 EA EA201892300A patent/EA036551B1/ru not_active IP Right Cessation
- 2017-04-21 BR BR112018070677-9A patent/BR112018070677B1/pt active IP Right Grant
- 2017-04-21 JP JP2018553226A patent/JP6894449B2/ja active Active
- 2017-04-21 RS RS20200549A patent/RS60257B1/sr unknown
- 2017-04-21 PE PE2018001558A patent/PE20181803A1/es unknown
- 2017-04-21 SM SM20200249T patent/SMT202000249T1/it unknown
- 2017-04-21 TW TW106113380A patent/TWI742074B/zh active
- 2017-04-21 AU AU2017252222A patent/AU2017252222B2/en active Active
- 2017-04-21 MA MA44721A patent/MA44721B1/fr unknown
- 2017-04-21 KR KR1020187033540A patent/KR102388208B1/ko active Active
- 2017-04-21 ES ES17720720T patent/ES2791319T3/es active Active
- 2017-04-21 AR ARP170101026A patent/AR108301A1/es active IP Right Grant
- 2017-04-21 SI SI201730246T patent/SI3445767T1/sl unknown
- 2017-04-21 MX MX2018012711A patent/MX386103B/es unknown
- 2017-04-21 PT PT177207206T patent/PT3445767T/pt unknown
- 2017-10-23 US US15/790,660 patent/US10196404B2/en active Active
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2018
- 2018-08-23 CL CL2018002410A patent/CL2018002410A1/es unknown
- 2018-09-12 SV SV2018005742A patent/SV2018005742A/es unknown
- 2018-09-25 NI NI201800093A patent/NI201800093A/es unknown
- 2018-10-05 DO DO2018000222A patent/DOP2018000222A/es unknown
- 2018-10-09 IL IL262237A patent/IL262237B/en unknown
- 2018-10-18 PH PH12018502227A patent/PH12018502227A1/en unknown
- 2018-11-19 ZA ZA2018/07766A patent/ZA201807766B/en unknown
- 2018-12-18 US US16/223,538 patent/US10889594B2/en active Active
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2020
- 2020-05-14 CY CY20201100443T patent/CY1123186T1/el unknown
- 2020-12-04 US US17/111,896 patent/US11472816B2/en active Active
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