MA30988B1 - Composes destines a inhiber la progression mitotique - Google Patents
Composes destines a inhiber la progression mitotiqueInfo
- Publication number
- MA30988B1 MA30988B1 MA31985A MA31985A MA30988B1 MA 30988 B1 MA30988 B1 MA 30988B1 MA 31985 A MA31985 A MA 31985A MA 31985 A MA31985 A MA 31985A MA 30988 B1 MA30988 B1 MA 30988B1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- mitotic progression
- inhibiting mitotic
- cancer
- treatment
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 230000002401 inhibitory effect Effects 0.000 title 1
- 230000008600 mitotic progression Effects 0.000 title 1
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 201000011510 cancer Diseases 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 102000004000 Aurora Kinase A Human genes 0.000 abstract 1
- 108090000461 Aurora Kinase A Proteins 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Enzymes And Modification Thereof (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
LA PRÉSENTE INVENTION CONCERNE DES COMPOSÉS REPRÉSENTÉS PAR LA FORMULE GÉNÉRALE (I), AINSI QUE DES PROCÉDÉS DESTINÉS AU TRAITEMENT DU CANCER. L'INVENTION CONCERNE PLUS PARTICULIÈREMENT DE PUISSANTS INHIBITEURS DE LA KINASE AURORA A, DES COMPOSITIONS PHARMACEUTIQUES COMPRENANT LES COMPOSÉS, AINSI QUE DES PROCÉDÉS D'UTILISATION DE CES COMPOSÉS POUR LE TRAITEMENT DU CANCER.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85934006P | 2006-11-16 | 2006-11-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30988B1 true MA30988B1 (fr) | 2009-12-01 |
Family
ID=39315133
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31985A MA30988B1 (fr) | 2006-11-16 | 2009-06-12 | Composes destines a inhiber la progression mitotique |
Country Status (34)
| Country | Link |
|---|---|
| US (7) | US8026246B2 (fr) |
| EP (4) | EP2086981B1 (fr) |
| JP (3) | JP5102839B2 (fr) |
| KR (2) | KR101342014B1 (fr) |
| CN (2) | CN101547924B (fr) |
| AR (1) | AR064246A1 (fr) |
| AT (1) | ATE556076T1 (fr) |
| AU (1) | AU2007322046B2 (fr) |
| BR (1) | BRPI0718803B8 (fr) |
| CA (1) | CA2669680C (fr) |
| CL (1) | CL2007003244A1 (fr) |
| CR (3) | CR10782A (fr) |
| CY (1) | CY1112828T1 (fr) |
| DK (2) | DK2497772T3 (fr) |
| EA (1) | EA015779B1 (fr) |
| ES (3) | ES2537451T3 (fr) |
| GE (1) | GEP20125459B (fr) |
| HR (2) | HRP20120490T1 (fr) |
| IL (1) | IL198690A0 (fr) |
| MA (1) | MA30988B1 (fr) |
| MX (3) | MX2009004670A (fr) |
| MY (1) | MY153243A (fr) |
| NO (1) | NO343338B1 (fr) |
| NZ (3) | NZ611898A (fr) |
| PH (1) | PH12012502057B1 (fr) |
| PL (2) | PL2497772T3 (fr) |
| PT (2) | PT2497772E (fr) |
| RS (2) | RS53788B1 (fr) |
| SG (2) | SG176443A1 (fr) |
| SI (2) | SI2086981T1 (fr) |
| TW (1) | TWI401255B (fr) |
| UA (1) | UA94129C2 (fr) |
| WO (1) | WO2008063525A1 (fr) |
| ZA (1) | ZA200903279B (fr) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104193750B (zh) | 2004-05-14 | 2018-04-27 | 千禧药品公司 | 通过抑制极光激酶抑制有丝分裂的化合物和方法 |
| CL2007003244A1 (es) * | 2006-11-16 | 2008-04-04 | Millennium Pharm Inc | Compuestos derivados de pirimido[5,4-d][2]benzazepina; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento del cancer. |
| WO2010065134A1 (fr) * | 2008-12-05 | 2010-06-10 | Millennium Pharmaceuticals, Inc. | 5, 7-dihydro- 6h-pyrimido [ 5, 4-d] [ 1 ] benzazépin-6-thiones utilisées en tant qu'inhibiteurs de plk |
| MX2011006725A (es) | 2008-12-22 | 2011-09-15 | Millennium Pharm Inc | Combinacion de inhibidores de aurora cinasa y anticuerpos anti-cd20. |
| JO3635B1 (ar) * | 2009-05-18 | 2020-08-27 | Millennium Pharm Inc | مركبات صيدلانية صلبة وطرق لانتاجها |
| JO3434B1 (ar) * | 2009-07-31 | 2019-10-20 | Millennium Pharm Inc | مركبات صيدلانية لمعالجة السرطان وامراض واضطرابات اخري |
| CN104031049A (zh) * | 2010-02-19 | 2014-09-10 | 米伦纽姆医药公司 | 极光激酶抑制剂的结晶形式 |
| US20120107304A1 (en) | 2010-04-27 | 2012-05-03 | Boehringer Ingelheim International Gmbh | Combination therapy in treatment of oncological and fibrotic diseases |
| WO2011161031A1 (fr) * | 2010-06-22 | 2011-12-29 | Glaxosmithkline Llc | Composés de benzotriazolodiazépine inhibiteurs de bromodomaines |
| AR086656A1 (es) * | 2011-06-03 | 2014-01-15 | Millennium Pharm Inc | Combinacion de inhibidores de mek e inhibidores selectivos de la quinasa aurora a |
| US20130303519A1 (en) * | 2012-03-20 | 2013-11-14 | Millennium Pharmaceuticals, Inc. | Methods of treating cancer using aurora kinase inhibitors |
| CN103772391A (zh) * | 2012-10-23 | 2014-05-07 | 杨子娇 | 一类治疗房角狭窄的化合物及其用途 |
| US9724354B2 (en) | 2013-03-22 | 2017-08-08 | Millennium Pharmaceuticals, Inc. | Combination of catalytic mTORC1/2 inhibitors and selective inhibitors of Aurora A kinase |
| WO2015085289A1 (fr) | 2013-12-06 | 2015-06-11 | Millennium Pharmaceuticals, Inc. | Combinaison d'inhibiteurs de kinase aurora et d'anticorps anti-cd30 |
| CA2972076A1 (fr) * | 2014-12-23 | 2016-06-30 | Millennium Pharmaceuticals, Inc. | Combinaison d'inhibiteurs de raf et d'inhibiteurs de kinases aurora |
| JP2018524292A (ja) | 2015-07-21 | 2018-08-30 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | オーロラキナーゼインヒビターと化学療法剤の投与 |
| CA2997769A1 (fr) | 2015-09-09 | 2017-03-16 | Icahn School Of Medicine At Mount Sinai | Sulfonamides heterocycliques tricycliques contraints en tant qu'agents anti-cancereux |
| CN108349961B (zh) | 2015-09-09 | 2022-02-18 | 西奈山伊坎医学院 | 杂环受限三环磺酰胺作为抗癌试剂 |
| US11340215B2 (en) | 2016-02-26 | 2022-05-24 | Japanese Foundation For Cancer Research | Screening method of anticancer agent focused on function of HP1 and evaluation system |
| CN109195593A (zh) | 2016-03-15 | 2019-01-11 | 奥莱松基因组股份有限公司 | 用于治疗实体瘤的lsd1抑制剂的组合 |
| JP6188986B1 (ja) * | 2017-03-23 | 2017-08-30 | 株式会社ノエビア | 時計遺伝子発現量調整剤及びエラスチン産生促進剤 |
| WO2019195658A1 (fr) | 2018-04-05 | 2019-10-10 | Dana-Farber Cancer Institute, Inc. | Niveaux sting comme biomarqueur pour l'immunothérapie du cancer |
| WO2020049208A1 (fr) | 2018-09-09 | 2020-03-12 | Fundacio Privada Institut De Recerca De La Sida - Caixa | Aurora cinasa comme cible pour traiter, prévenir ou soigner une infection par vih ou le sida |
| US20220305048A1 (en) | 2019-08-26 | 2022-09-29 | Dana-Farber Cancer Institute, Inc. | Use of heparin to promote type 1 interferon signaling |
| WO2023196959A1 (fr) | 2022-04-07 | 2023-10-12 | Eli Lilly And Company | Procédé de fabrication d'un inhibiteur de kras g12c |
| WO2023196887A1 (fr) | 2022-04-08 | 2023-10-12 | Eli Lilly And Company | Méthode de traitement comprenant des inhibiteurs de kras g12c et des inhibiteurs d'aurora a |
| IL317823A (en) | 2022-06-30 | 2025-02-01 | Lilly Co Eli | KRAS G12C inhibitor for cancer treatment |
| WO2025075211A1 (fr) | 2023-10-03 | 2025-04-10 | Takeda Pharmaceutical Company Limited | Alisertib et paclitaxel pour le traitement du cancer du poumon à petites cellules |
| WO2025245045A1 (fr) | 2024-05-21 | 2025-11-27 | The Regents Of The University Of California | Méthodes de traitement du cancer du poumon |
Family Cites Families (27)
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| US4099012A (en) * | 1975-08-28 | 1978-07-04 | Ciba-Geigy Corporation | 2-pyrazolyl-benzophenones |
| SU1181547A3 (ru) | 1979-02-07 | 1985-09-23 | Ф.Хоффманн-Ля Рош Унд Ко,Аг (Фирма) | Способ получени пиримидо-2-бензазепинов или их фармакологически совместимых кислотно-аддитивных солей (и его вариант) |
| US4481142A (en) * | 1979-02-07 | 1984-11-06 | Hoffmann-La Roche Inc. | Pyrimido-2-benzazepines |
| US4469633A (en) * | 1980-05-16 | 1984-09-04 | Hoffmann-La Roche Inc. | N-oxides of 5-oxo-1-phenyl-2-benzazepines |
| EP0273697A3 (fr) | 1986-12-30 | 1989-11-29 | Merck & Co. Inc. | 2-Benzazépines à cycles hétérocycliques de 5 et 6 côtés |
| US5166151A (en) * | 1988-03-25 | 1992-11-24 | Merck & Co., Inc. | 2-Benzazepines with 5- and 6-membered heterocyclic rings, compositions and medical methods of use thereof |
| US5210082A (en) * | 1991-05-16 | 1993-05-11 | Merck & Co., Inc. | 2-benzazepines with 5- and 6-membered heterocyclic rings to treat pain and anxiety disorders |
| GB9523675D0 (en) | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
| AU723860B2 (en) | 1996-03-08 | 2000-09-07 | Astrazeneca Ab | Azolobenzazepine derivatives as neurologically active agents |
| AU5330698A (en) * | 1996-12-23 | 1998-07-17 | Celltech Therapeutics Limited | Fused polycyclic 2-aminopyrimidine derivatives, their preparation and their use as protein tyrosine kinase inhibitors |
| GB9713087D0 (en) | 1997-06-20 | 1997-08-27 | Celltech Therapeutics Ltd | Chemical compounds |
| TW510902B (en) * | 1997-09-29 | 2002-11-21 | Meiji Seika Kaisha | Tricyclic triazolobenzazepine derivatives, process for producing the same, and antiallergic agents |
| US6277844B1 (en) * | 1998-09-14 | 2001-08-21 | Sydney Spector | Compound for selective treatment of malignant cells by inhibiting cell cycle progression, decreasing Bcl2, and increasing apoptosis |
| US6417207B1 (en) | 1999-05-12 | 2002-07-09 | Nitromed, Inc. | Nitrosated and nitrosylated potassium channel activators, compositions and methods of use |
| AU1651201A (en) | 1999-12-06 | 2001-06-18 | Ajinomoto Co., Inc. | Amidinophenylpyruvic acid derivative |
| CN102250071A (zh) * | 2000-12-21 | 2011-11-23 | 沃泰克斯药物股份有限公司 | 可用作蛋白激酶抑制剂的吡唑化合物 |
| US6686352B2 (en) | 2001-05-18 | 2004-02-03 | Hoffmann-La Roche Inc. | Substituted imidazo [1,5-a] pyrimido [5,4-d] [1] benzazepine derivatives |
| DE10135457A1 (de) * | 2001-07-20 | 2003-02-06 | Adc Automotive Dist Control | Optische Sensoranordnung |
| AU2002328999B8 (en) | 2001-08-09 | 2008-06-05 | Actelion Pharmaceuticals Ltd. | Novel benzo-fused heterocycles as endothelin antagonists |
| CN1897950A (zh) | 2003-10-14 | 2007-01-17 | 惠氏公司 | 稠合芳基和杂芳基衍生物及其使用方法 |
| CN104193750B (zh) * | 2004-05-14 | 2018-04-27 | 千禧药品公司 | 通过抑制极光激酶抑制有丝分裂的化合物和方法 |
| RU2007122485A (ru) | 2004-11-17 | 2008-12-27 | Мийкана Терапьютикс | Ингибиторы киназы |
| US20100160324A1 (en) | 2004-12-30 | 2010-06-24 | Astex Therapeutics Limited | Pyrazole derivatives as that modulate the activity of cdk, gsk and aurora kinases |
| ES2408318T3 (es) | 2005-12-23 | 2013-06-20 | Glaxosmithkline Llc | Inhibidores de azaindol de las cinasas Aurora |
| JP2010500352A (ja) | 2006-08-09 | 2010-01-07 | ミレニアム・ファーマシューティカルズ・インコーポレイテッド | 有糸分裂の進行を阻止するためのピリドベンゾアゼピン化合物および方法 |
| CL2007003244A1 (es) | 2006-11-16 | 2008-04-04 | Millennium Pharm Inc | Compuestos derivados de pirimido[5,4-d][2]benzazepina; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento del cancer. |
| JO3635B1 (ar) | 2009-05-18 | 2020-08-27 | Millennium Pharm Inc | مركبات صيدلانية صلبة وطرق لانتاجها |
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2007
- 2007-11-09 CL CL200703244A patent/CL2007003244A1/es unknown
- 2007-11-14 NZ NZ611898A patent/NZ611898A/en not_active IP Right Cessation
- 2007-11-14 RS RS20150047A patent/RS53788B1/sr unknown
- 2007-11-14 MX MX2009004670A patent/MX2009004670A/es active IP Right Grant
- 2007-11-14 EA EA200970486A patent/EA015779B1/ru unknown
- 2007-11-14 TW TW096143087A patent/TWI401255B/zh active
- 2007-11-14 EP EP07867449A patent/EP2086981B1/fr active Active
- 2007-11-14 CN CN2007800423837A patent/CN101547924B/zh active Active
- 2007-11-14 SG SG2011080652A patent/SG176443A1/en unknown
- 2007-11-14 DK DK12153131.3T patent/DK2497772T3/en active
- 2007-11-14 SI SI200730975T patent/SI2086981T1/sl unknown
- 2007-11-14 US US11/985,277 patent/US8026246B2/en active Active
- 2007-11-14 GE GEAP200711309A patent/GEP20125459B/en unknown
- 2007-11-14 KR KR1020117022355A patent/KR101342014B1/ko active Active
- 2007-11-14 PL PL12153131T patent/PL2497772T3/pl unknown
- 2007-11-14 JP JP2009537199A patent/JP5102839B2/ja active Active
- 2007-11-14 DK DK07867449.6T patent/DK2086981T3/da active
- 2007-11-14 EP EP15155821.0A patent/EP2944639B1/fr active Active
- 2007-11-14 BR BRPI0718803A patent/BRPI0718803B8/pt active IP Right Grant
- 2007-11-14 EP EP12153134.7A patent/EP2497773B1/fr active Active
- 2007-11-14 CA CA2669680A patent/CA2669680C/fr active Active
- 2007-11-14 AT AT07867449T patent/ATE556076T1/de active
- 2007-11-14 PL PL07867449T patent/PL2086981T3/pl unknown
- 2007-11-14 HR HRP20120490TT patent/HRP20120490T1/hr unknown
- 2007-11-14 KR KR1020097012501A patent/KR101110458B1/ko active Active
- 2007-11-14 ZA ZA200903279A patent/ZA200903279B/xx unknown
- 2007-11-14 RS RS20120247A patent/RS52313B/sr unknown
- 2007-11-14 MX MX2012011398A patent/MX343391B/es unknown
- 2007-11-14 ES ES12153134.7T patent/ES2537451T3/es active Active
- 2007-11-14 NZ NZ577042A patent/NZ577042A/en unknown
- 2007-11-14 ES ES12153131.3T patent/ES2528793T3/es active Active
- 2007-11-14 SG SG10201503350TA patent/SG10201503350TA/en unknown
- 2007-11-14 SI SI200731591T patent/SI2497772T1/sl unknown
- 2007-11-14 MX MX2012011396A patent/MX348568B/es unknown
- 2007-11-14 EP EP12153131.3A patent/EP2497772B1/fr active Active
- 2007-11-14 WO PCT/US2007/023948 patent/WO2008063525A1/fr not_active Ceased
- 2007-11-14 NZ NZ597252A patent/NZ597252A/xx unknown
- 2007-11-14 ES ES07867449T patent/ES2384123T3/es active Active
- 2007-11-14 PT PT121531313T patent/PT2497772E/pt unknown
- 2007-11-14 CN CN201310367332.9A patent/CN103483343B/zh active Active
- 2007-11-14 AU AU2007322046A patent/AU2007322046B2/en active Active
- 2007-11-14 MY MYPI20091846A patent/MY153243A/en unknown
- 2007-11-14 UA UAA200906211A patent/UA94129C2/ru unknown
- 2007-11-14 PT PT07867449T patent/PT2086981E/pt unknown
- 2007-11-16 AR ARP070105104A patent/AR064246A1/es unknown
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2009
- 2009-05-08 CR CR10782A patent/CR10782A/es unknown
- 2009-05-11 IL IL198690A patent/IL198690A0/en active IP Right Grant
- 2009-05-13 NO NO20091864A patent/NO343338B1/no unknown
- 2009-06-12 MA MA31985A patent/MA30988B1/fr unknown
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2011
- 2011-08-25 US US13/217,729 patent/US9988384B2/en active Active
- 2011-08-25 US US13/217,659 patent/US20110312942A1/en not_active Abandoned
- 2011-08-30 JP JP2011187930A patent/JP5452811B2/ja active Active
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2012
- 2012-06-06 CY CY20121100518T patent/CY1112828T1/el unknown
- 2012-10-12 PH PH12012502057A patent/PH12012502057B1/en unknown
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2013
- 2013-11-15 JP JP2013236439A patent/JP2014055166A/ja active Pending
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2014
- 2014-04-04 CR CR20140154A patent/CR20140154A/es unknown
- 2014-10-15 US US14/514,687 patent/US9765076B2/en active Active
- 2014-11-27 CR CR20140544A patent/CR20140544A/es unknown
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2015
- 2015-01-13 HR HRP20150047TT patent/HRP20150047T1/hr unknown
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2018
- 2018-06-01 US US15/996,166 patent/US10836766B2/en active Active
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2020
- 2020-11-16 US US17/099,266 patent/US11958855B2/en active Active
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2024
- 2024-03-07 US US18/598,629 patent/US20240400567A1/en active Pending
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