MA57399B1 - Inhibition de l'intégrine humaine alpha4beta7 - Google Patents
Inhibition de l'intégrine humaine alpha4beta7Info
- Publication number
- MA57399B1 MA57399B1 MA57399A MA57399A MA57399B1 MA 57399 B1 MA57399 B1 MA 57399B1 MA 57399 A MA57399 A MA 57399A MA 57399 A MA57399 A MA 57399A MA 57399 B1 MA57399 B1 MA 57399B1
- Authority
- MA
- Morocco
- Prior art keywords
- integrin
- inhibition
- human
- diseases
- treat
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Radio Relay Systems (AREA)
- Air Conditioning Control Device (AREA)
- Indole Compounds (AREA)
Abstract
L'invention concerne des petites molécules antagonistes de l'intégrine α4β7 et des procédés d'utilisation de celles-ci pour traiter un certain nombre de maladies et de pathologies.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962916062P | 2019-10-16 | 2019-10-16 | |
| PCT/US2020/055986 WO2021076890A1 (fr) | 2019-10-16 | 2020-10-16 | INHIBITION DE L'INTÉGRINE HUMAINE α4β7 |
| EP20875989.4A EP4045039B1 (fr) | 2019-10-16 | 2020-10-16 | Inhibition de l'intégrine humaine alpha4beta7 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA57399B1 true MA57399B1 (fr) | 2025-06-30 |
Family
ID=73198501
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA57399A MA57399B1 (fr) | 2019-10-16 | 2020-10-16 | Inhibition de l'intégrine humaine alpha4beta7 |
Country Status (37)
| Country | Link |
|---|---|
| US (3) | US11104661B1 (fr) |
| EP (3) | EP4045039B1 (fr) |
| JP (7) | JP7437490B2 (fr) |
| KR (2) | KR20220102669A (fr) |
| CN (3) | CN115087444B (fr) |
| AR (1) | AR120244A1 (fr) |
| AU (2) | AU2020366435A1 (fr) |
| BR (1) | BR112022007284A2 (fr) |
| CA (1) | CA3154269A1 (fr) |
| CL (1) | CL2022000959A1 (fr) |
| CO (1) | CO2022005759A2 (fr) |
| CR (1) | CR20220205A (fr) |
| CU (1) | CU20220027A7 (fr) |
| DK (1) | DK4045039T3 (fr) |
| DO (2) | DOP2022000081A (fr) |
| EC (1) | ECSP22038978A (fr) |
| ES (1) | ES3035561T3 (fr) |
| FI (1) | FI4045039T3 (fr) |
| HR (1) | HRP20250749T1 (fr) |
| HU (1) | HUE071814T2 (fr) |
| IL (2) | IL319053A (fr) |
| LT (1) | LT4045039T (fr) |
| MA (1) | MA57399B1 (fr) |
| MD (1) | MD4045039T2 (fr) |
| MX (1) | MX2022004406A (fr) |
| PE (1) | PE20221829A1 (fr) |
| PH (1) | PH12022550886A1 (fr) |
| PL (1) | PL4045039T3 (fr) |
| PT (1) | PT4045039T (fr) |
| PY (1) | PY2065718A (fr) |
| RS (1) | RS66976B1 (fr) |
| SI (1) | SI4045039T1 (fr) |
| TW (7) | TWI857592B (fr) |
| UA (1) | UA130059C2 (fr) |
| UY (1) | UY38926A (fr) |
| WO (3) | WO2021076890A1 (fr) |
| ZA (2) | ZA202203872B (fr) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7365358B2 (ja) | 2018-04-12 | 2023-10-19 | モーフィック セラピューティック,インコーポレイテッド | ヒトインテグリンα4β7のアンタゴニスト |
| EP4541422A3 (fr) | 2018-10-30 | 2025-06-25 | Gilead Sciences, Inc. | Dérivés de quinoléine utilisés en tant qu'inhibiteurs de l'intégrine alpha4bêta7 |
| AU2020276277B2 (en) | 2019-05-15 | 2025-03-20 | Chemocentryx, Inc. | Triaryl compounds for treatment of PD-L1 diseases |
| KR102908219B1 (ko) | 2019-08-14 | 2026-01-08 | 길리애드 사이언시즈, 인코포레이티드 | 알파 4 베타 7 인테그린의 저해용 화합물 |
| CN114555080B (zh) | 2019-10-16 | 2025-10-10 | 凯莫森特里克斯股份有限公司 | 用于治疗pd-l1疾病的杂芳基联苯胺 |
| WO2021076890A1 (fr) * | 2019-10-16 | 2021-04-22 | Morphic Therapeutic, Inc. | INHIBITION DE L'INTÉGRINE HUMAINE α4β7 |
| AU2020368393B2 (en) | 2019-10-16 | 2026-01-08 | Chemocentryx, Inc. | Heteroaryl-biphenyl amides for the treatment of PD-L1 diseases |
| CN118591535A (zh) * | 2021-12-27 | 2024-09-03 | 西藏海思科制药有限公司 | 一种丙酸衍生物及其在医药上的应用 |
| JP2025530250A (ja) | 2022-09-09 | 2025-09-11 | シーザン ハイスーク ファーマシューティカル カンパニー リミテッド | プロピオン酸誘導体及びその医薬的な応用 |
| KR20250120367A (ko) | 2022-12-22 | 2025-08-08 | 신테라, 인크. | 알파4 베타7 인테그린 안타고니스트 및 이의 용도 |
| JP2026506997A (ja) * | 2023-02-21 | 2026-02-27 | シーフォーエックス・ディスカバリー・リミテッド | 大環状アルファ4ベータ7インテグリン阻害剤 |
| IL324720A (en) | 2023-05-26 | 2026-01-01 | Adarx Pharmaceuticals Inc | SOD1 modulators and methods of using them |
| CN121712771A (zh) | 2023-07-28 | 2026-03-20 | 上海翰森生物医药科技有限公司 | 一种苯并含氮杂环类衍生物调节剂、其制备方法和应用 |
| WO2025026955A1 (fr) * | 2023-07-28 | 2025-02-06 | Galapagos Nv | Nouveaux composés et compositions pharmaceutiques de ceux-ci pour le traitement de troubles inflammatoires |
| WO2025176107A1 (fr) * | 2024-02-20 | 2025-08-28 | 西藏海思科制药有限公司 | Dérivés de pyridone et leur utilisation médicale |
| CN118702712B (zh) * | 2024-07-04 | 2025-11-11 | 安徽普利药业有限公司 | 一种n-(3-苯10硼酸)-l-天冬氨酸中间体制备方法 |
| WO2026018016A1 (fr) * | 2024-07-19 | 2026-01-22 | C4X Discovery Limited | Composés thérapeutiques |
| WO2026018017A1 (fr) * | 2024-07-19 | 2026-01-22 | C4X Discovery Limited | Composés thérapeutiques |
| CN119504796B (zh) * | 2024-11-20 | 2026-03-10 | 南通大学附属医院 | 一种具有抗肿瘤活性的化合物及其应用 |
Family Cites Families (44)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CA2159450C (fr) | 1993-03-31 | 2002-01-08 | Norman Anthony Abood | 1-amidinophenyl-pyrrolidones piperidinones azetinones, inhibiteurs de l'agregation plaquettaire |
| DE4427979A1 (de) | 1993-11-15 | 1996-02-15 | Cassella Ag | Substituierte 5-Ring-Heterocyclen, ihre Herstellung und ihre Verwendung |
| US5849736A (en) | 1993-11-24 | 1998-12-15 | The Dupont Merck Pharmaceutical Company | Isoxazoline and isoxazole fibrinogen receptor antagonists |
| DE19622489A1 (de) | 1996-06-05 | 1997-12-11 | Hoechst Ag | Salze des 3-(2-(4-(4-(Amino-imino-methyl)-phenyl)-4- methyl-2,5-dioxo-imidazolidin-1-yl)-acetylamino)-3- phenyl-propionsäure-ethylesters |
| EP0932615A1 (fr) | 1996-10-11 | 1999-08-04 | Cor Therapeutics, Inc. | INHIBITEURS SELECTIFS DU FACTEUR Xa |
| WO1998016524A1 (fr) | 1996-10-11 | 1998-04-23 | Cor Therapeutics, Inc. | DERIVES HETEROCYCLIQUES UTILISES COMME INHIBITEURS DE FACTEUR Xa |
| DE19751251A1 (de) | 1997-11-19 | 1999-05-20 | Hoechst Marion Roussel De Gmbh | Substituierte Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmezeutische Präparate |
| AU751950B2 (en) * | 1997-11-24 | 2002-09-05 | Merck & Co., Inc. | Substituted beta-alanine derivatives as cell adhesion inhibitors |
| US6645939B1 (en) | 1997-11-24 | 2003-11-11 | Merck & Co., Inc. | Substituted β-alanine derivatives as cell adhesion inhibitors |
| MY153569A (en) | 1998-01-20 | 2015-02-27 | Mitsubishi Tanabe Pharma Corp | Inhibitors of ?4 mediated cell adhesion |
| DE19821483A1 (de) | 1998-05-14 | 1999-11-18 | Hoechst Marion Roussel De Gmbh | Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate |
| CA2333647A1 (fr) | 1998-06-29 | 2000-01-06 | Dupont Pharmaceuticals Company | Isoxazolidines et carbamates cycliques utilises comme antagonistes de iib/iiia |
| AU747784B2 (en) * | 1998-07-29 | 2002-05-23 | Merck & Co., Inc. | Integrin receptor antagonists |
| GB9826174D0 (en) * | 1998-11-30 | 1999-01-20 | Celltech Therapeutics Ltd | Chemical compounds |
| US6972296B2 (en) | 1999-05-07 | 2005-12-06 | Encysive Pharmaceuticals Inc. | Carboxylic acid derivatives that inhibit the binding of integrins to their receptors |
| US6723711B2 (en) * | 1999-05-07 | 2004-04-20 | Texas Biotechnology Corporation | Propanoic acid derivatives that inhibit the binding of integrins to their receptors |
| BR0010349B1 (pt) * | 1999-05-07 | 2011-10-04 | derivados de ácido propanóico que inibem a ligação de integrinas aos seus receptores. | |
| CA2385882C (fr) | 1999-09-24 | 2009-11-24 | Genentech, Inc. | Derives de tyrosine |
| DE10041423A1 (de) | 2000-08-23 | 2002-03-07 | Merck Patent Gmbh | Biphenylderivate |
| AU2001288515A1 (en) * | 2000-08-30 | 2002-03-13 | Pharmacia Corporation | Gem-substituted alpha v beta 3 integrin antagonists |
| DE10111876A1 (de) | 2001-03-10 | 2002-09-19 | Aventis Pharma Gmbh | Bis(trifluormethyl)hydantoine als Zwischenprodukte für pharmazeutische Wirkstoffe |
| DE10154280A1 (de) | 2001-11-05 | 2003-05-15 | Wilex Ag | Antagonisten für alpha¶4¶-Integrine |
| PL215263B1 (pl) | 2002-02-25 | 2013-11-29 | Elan Pharm Inc | Kompozycja do przewleklego leczenia patologicznego zapalenia i zastosowanie natalizumabu lub jego immunologicznie aktywnego fragmentu do wytwarzania leku |
| RS52213B (sr) | 2004-09-03 | 2012-10-31 | Genentech, Inc. | Humanizovani anti-beta7 antagonisti i njihove primene |
| ES2387317T3 (es) | 2005-03-03 | 2012-09-20 | Seedlings Life Science Ventures, Llc. | Procedimiento de control de riesgos de pacientes en tratamiento con natalizumab |
| WO2006126529A1 (fr) | 2005-05-25 | 2006-11-30 | Shionogi & Co., Ltd. | Derive de morphinane substitue en position 7 par un carbamoyle et insature en positions 6 et 7 |
| AU2006254772B2 (en) | 2005-06-09 | 2011-06-02 | Ucb Pharma S.A. | 2,6 quinolinyl derivatives, processes for preparing them and their use as medicament |
| ES2752137T3 (es) | 2006-02-28 | 2020-04-03 | Biogen Ma Inc | Métodos para tratar enfermedades inflamatorias y autoinmunes con natalizumab |
| US20100272680A1 (en) | 2009-02-09 | 2010-10-28 | Subramanian Baskaran | Piperidinyl Cyclic Amido Antiviral Agents |
| EP3412309A1 (fr) | 2011-03-31 | 2018-12-12 | F. Hoffmann-La Roche AG | Procédés d'administration d'antagonistes de l'intégrine bêta7 |
| EP2903691B1 (fr) | 2012-10-05 | 2019-05-22 | F.Hoffmann-La Roche Ag | Méthodes de diagnostic et de traitement de maladie intestinale inflammatoire |
| KR20220065091A (ko) | 2014-03-27 | 2022-05-19 | 제넨테크, 인크. | 염증성 장 질환의 진단 및 치료 방법 |
| WO2016011940A1 (fr) | 2014-07-25 | 2016-01-28 | 江苏恒瑞医药股份有限公司 | Dérivé d'indole-amide, son procédé de préparation et son application en médecine |
| WO2016086147A1 (fr) * | 2014-11-26 | 2016-06-02 | Millennium Pharmaceuticals, Inc. | Vedolizumab utilisable en vue du traitement de la maladie de crohn fistulisante |
| KR20170120601A (ko) | 2015-02-26 | 2017-10-31 | 제넨테크, 인크. | 인테그린 베타7 길항제 및 크론병을 치료하는 방법 |
| MA47697A (fr) * | 2017-02-28 | 2020-01-08 | Morphic Therapeutic Inc | Inhibiteurs de l'(alpha-v)(bêta-6) intégrine |
| US10246451B2 (en) | 2017-04-26 | 2019-04-02 | Aviara Pharmaceuticals, Inc. | Propionic acid derivatives and methods of use thereof |
| US10875875B2 (en) * | 2017-04-26 | 2020-12-29 | Aviara Pharmaceuticals, Inc. | Propionic acid derivatives and methods of use thereof |
| JP7365358B2 (ja) * | 2018-04-12 | 2023-10-19 | モーフィック セラピューティック,インコーポレイテッド | ヒトインテグリンα4β7のアンタゴニスト |
| KR102659859B1 (ko) | 2018-10-30 | 2024-04-25 | 길리애드 사이언시즈, 인코포레이티드 | 알파4β7 인테그린의 억제를 위한 화합물 |
| EP4541422A3 (fr) | 2018-10-30 | 2025-06-25 | Gilead Sciences, Inc. | Dérivés de quinoléine utilisés en tant qu'inhibiteurs de l'intégrine alpha4bêta7 |
| AU2019373242B2 (en) * | 2018-10-30 | 2023-07-13 | Gilead Sciences, Inc. | Compounds for inhibition of alpha 4 beta 7 integrin |
| CN112969700B (zh) | 2018-10-30 | 2024-08-20 | 吉利德科学公司 | 作为α4β7整合素抑制剂的咪唑并吡啶衍生物 |
| WO2021076890A1 (fr) * | 2019-10-16 | 2021-04-22 | Morphic Therapeutic, Inc. | INHIBITION DE L'INTÉGRINE HUMAINE α4β7 |
-
2020
- 2020-10-16 WO PCT/US2020/055986 patent/WO2021076890A1/fr not_active Ceased
- 2020-10-16 EP EP20875989.4A patent/EP4045039B1/fr active Active
- 2020-10-16 JP JP2022509595A patent/JP7437490B2/ja active Active
- 2020-10-16 PE PE2022000633A patent/PE20221829A1/es unknown
- 2020-10-16 BR BR112022007284A patent/BR112022007284A2/pt unknown
- 2020-10-16 CR CR20220205A patent/CR20220205A/es unknown
- 2020-10-16 SI SI202030622T patent/SI4045039T1/sl unknown
- 2020-10-16 PL PL20875989.4T patent/PL4045039T3/pl unknown
- 2020-10-16 JP JP2022523102A patent/JP7437495B2/ja active Active
- 2020-10-16 EP EP25157767.2A patent/EP4559525A3/fr active Pending
- 2020-10-16 CA CA3154269A patent/CA3154269A1/fr active Pending
- 2020-10-16 AR ARP200102870A patent/AR120244A1/es unknown
- 2020-10-16 HR HRP20250749TT patent/HRP20250749T1/hr unknown
- 2020-10-16 US US17/072,797 patent/US11104661B1/en active Active
- 2020-10-16 TW TW112116098A patent/TWI857592B/zh active
- 2020-10-16 CN CN202080088450.4A patent/CN115087444B/zh active Active
- 2020-10-16 ES ES20875989T patent/ES3035561T3/es active Active
- 2020-10-16 TW TW111127993A patent/TWI802477B/zh active
- 2020-10-16 MX MX2022004406A patent/MX2022004406A/es unknown
- 2020-10-16 US US17/769,003 patent/US20240174632A1/en active Pending
- 2020-10-16 PH PH1/2022/550886A patent/PH12022550886A1/en unknown
- 2020-10-16 WO PCT/US2020/056001 patent/WO2021076902A1/fr not_active Ceased
- 2020-10-16 RS RS20250645A patent/RS66976B1/sr unknown
- 2020-10-16 PY PY202002065718A patent/PY2065718A/es unknown
- 2020-10-16 CU CU2022000027A patent/CU20220027A7/es unknown
- 2020-10-16 CN CN202411308053.XA patent/CN119192137A/zh active Pending
- 2020-10-16 UA UAA202201185A patent/UA130059C2/uk unknown
- 2020-10-16 TW TW109136036A patent/TWI775182B/zh active
- 2020-10-16 DK DK20875989.4T patent/DK4045039T3/da active
- 2020-10-16 UY UY0001038926A patent/UY38926A/es unknown
- 2020-10-16 KR KR1020227015040A patent/KR20220102669A/ko active Pending
- 2020-10-16 PT PT208759894T patent/PT4045039T/pt unknown
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