MX2012000682A - Formas de bases libres cristalinas de un compuesto de bifenilo. - Google Patents
Formas de bases libres cristalinas de un compuesto de bifenilo.Info
- Publication number
- MX2012000682A MX2012000682A MX2012000682A MX2012000682A MX2012000682A MX 2012000682 A MX2012000682 A MX 2012000682A MX 2012000682 A MX2012000682 A MX 2012000682A MX 2012000682 A MX2012000682 A MX 2012000682A MX 2012000682 A MX2012000682 A MX 2012000682A
- Authority
- MX
- Mexico
- Prior art keywords
- crystalline
- crystalline freebase
- biphenyl compound
- freebases
- freebase forms
- Prior art date
Links
- 239000012458 free base Substances 0.000 title abstract 3
- 235000010290 biphenyl Nutrition 0.000 title 1
- 239000004305 biphenyl Substances 0.000 title 1
- -1 biphenyl compound Chemical class 0.000 title 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 title 1
- QMOVGVNKXUTCQU-UHFFFAOYSA-N (2-phenylphenyl)carbamic acid Chemical compound OC(=O)NC1=CC=CC=C1C1=CC=CC=C1 QMOVGVNKXUTCQU-UHFFFAOYSA-N 0.000 abstract 1
- 208000019693 Lung disease Diseases 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D211/62—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/12—Aerosols; Foams
- A61K9/124—Aerosols; Foams characterised by the propellant
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
- A61K9/1623—Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D211/62—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
- C07D211/64—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4 having an aryl radical as the second substituent in position 4
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Dispersion Chemistry (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Dos formas de bases libres cristalinas del éster 1-(2-[4-(4-carbamilpiperidin-l-ilmetil)benzoíl]metilamino}etil)pi peridin-4-ílico de ácido bifenil-2-ilcarbámico. Composiciones farmacéuticas que comprenden estas bases libres cristalinas o que se preparan usando estas bases libres cristalinas. Procesos e intermediarios para preparar estas bases libres cristalinas. Métodos para usar estas bases libres cristalinas en el tratamiento de los trastornos pulmonares.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22580309P | 2009-07-15 | 2009-07-15 | |
| PCT/US2010/041903 WO2011008809A1 (en) | 2009-07-15 | 2010-07-14 | Crystalline freebase forms of a biphenyl compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2012000682A true MX2012000682A (es) | 2012-02-28 |
Family
ID=42562758
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2012000682A MX2012000682A (es) | 2009-07-15 | 2010-07-14 | Formas de bases libres cristalinas de un compuesto de bifenilo. |
Country Status (20)
| Country | Link |
|---|---|
| US (12) | US8541451B2 (es) |
| EP (2) | EP2987490B1 (es) |
| JP (4) | JP5651174B2 (es) |
| KR (1) | KR101742252B1 (es) |
| CN (1) | CN102470130B (es) |
| AU (1) | AU2010273514B2 (es) |
| BR (1) | BR112012000890A2 (es) |
| CA (2) | CA2989129C (es) |
| DK (1) | DK2453894T3 (es) |
| ES (2) | ES2639642T3 (es) |
| HR (1) | HRP20151344T1 (es) |
| HU (1) | HUE026414T2 (es) |
| IL (1) | IL216995A (es) |
| MX (1) | MX2012000682A (es) |
| PL (2) | PL2453894T3 (es) |
| PT (1) | PT2453894E (es) |
| SG (2) | SG10201407913UA (es) |
| SI (1) | SI2453894T1 (es) |
| SM (1) | SMT201600019B (es) |
| WO (1) | WO2011008809A1 (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI341836B (en) | 2004-03-11 | 2011-05-11 | Theravance Inc | Biphenyl compounds useful as muscarinic receptor antagonists |
| MX2012000682A (es) | 2009-07-15 | 2012-02-28 | Theravance Inc | Formas de bases libres cristalinas de un compuesto de bifenilo. |
| SG186708A1 (en) * | 2010-07-13 | 2013-02-28 | Theravance Inc | Process for preparing a biphenyl-2-ylcarbamic acid |
| TR201816077T4 (tr) * | 2013-02-21 | 2018-11-21 | Pfizer | Seçici bir cdk4/6 inhibitörünün katı formları. |
| WO2015070366A1 (en) | 2013-11-12 | 2015-05-21 | Merck Sharp & Dohme Corp. | Aryl linked imidazole and triazole derivatives and methods of use thereof for improving the pharmacokinetics of a drug |
| WO2020047225A1 (en) | 2018-08-30 | 2020-03-05 | Theravance Biopharma R&D Ip, Llc | Methods for treating chronic obstructive pulmonary disease |
| CN112694434B (zh) * | 2020-12-29 | 2023-06-16 | 浙江和泽医药科技股份有限公司 | 一种雷芬那辛新中间体及其活性亲电砌块和雷芬那辛的新制备方法 |
| CN118401497A (zh) | 2021-12-09 | 2024-07-26 | 医药化学公司 | 雷芬那辛的结晶型丙酮溶剂化物 |
| CN114276290B (zh) * | 2021-12-24 | 2024-05-28 | 浙江和泽医药科技股份有限公司 | 一种雷芬那辛无水晶型及其制备方法 |
| CN117263848A (zh) * | 2023-09-19 | 2023-12-22 | 山东京卫制药有限公司 | 一种雷芬那辛的吸入喷雾剂 |
| CN117180235A (zh) * | 2023-09-19 | 2023-12-08 | 山东京卫制药有限公司 | 一种无定型雷芬那辛吸入制剂 |
| CN117263849A (zh) * | 2023-09-19 | 2023-12-22 | 山东京卫制药有限公司 | 一种雷芬那辛三水合物晶型及其制备方法 |
| US20250136550A1 (en) | 2023-10-27 | 2025-05-01 | Theravance Biopharma R&D Ip, Llc | Processes for preparing revefenacin and compositions comprising the same |
| CN119775192B (zh) * | 2024-12-31 | 2025-11-28 | 山东京卫制药有限公司 | 一种三苯乙酸雷芬那辛晶型及其制备方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| DE2425983C3 (de) * | 1973-06-12 | 1978-09-14 | Toyama Chemical Co. Ltd., Tokio | Sulfonsäuresalze von Acylcholinen, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Zusammensetzung |
| BR8007911A (pt) | 1979-12-06 | 1981-06-16 | Glaxo Group Ltd | Inalador aperfeicoado |
| ATE23272T1 (de) | 1981-07-08 | 1986-11-15 | Draco Ab | Pulverinhalator. |
| NZ217006A (en) | 1985-07-30 | 1989-04-26 | Glaxo Group Ltd | Inhaler for finely divided medicament includes plunger to open medicament container |
| US5225183A (en) | 1988-12-06 | 1993-07-06 | Riker Laboratories, Inc. | Medicinal aerosol formulations |
| HU213221B (en) | 1990-03-02 | 1997-03-28 | Glaxo Group Ltd | Inhalation device and medicine packet for device |
| US6006745A (en) | 1990-12-21 | 1999-12-28 | Minnesota Mining And Manufacturing Company | Device for delivering an aerosol |
| US5874063A (en) | 1991-04-11 | 1999-02-23 | Astra Aktiebolag | Pharmaceutical formulation |
| WO1992022286A1 (en) | 1991-06-12 | 1992-12-23 | Minnesota Mining And Manufacturing Company | Albuterol sulfate suspension aerosol formulations |
| US5337740A (en) | 1991-08-01 | 1994-08-16 | New England Pharmaceuticals, Inc. | Inhalation devices |
| EP0717987B1 (en) | 1991-12-18 | 2001-08-29 | Minnesota Mining And Manufacturing Company | Suspension aerosol formulations |
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| US5415162A (en) | 1994-01-18 | 1995-05-16 | Glaxo Inc. | Multi-dose dry powder inhalation device |
| CA2182568A1 (en) | 1994-02-10 | 1995-08-17 | Makoto Takeuchi | Novel carbamate derivative and medicinal composition containing the same |
| US5983956A (en) | 1994-10-03 | 1999-11-16 | Astra Aktiebolag | Formulation for inhalation |
| US5637820A (en) * | 1995-01-06 | 1997-06-10 | Wittman; Kenneth L. | Stringed instrument with on-board tuner |
| SE9501384D0 (sv) | 1995-04-13 | 1995-04-13 | Astra Ab | Process for the preparation of respirable particles |
| BR9604977A (pt) | 1995-04-14 | 1998-06-09 | Glaxo Wellcome Inc | Inalador de dose medida sistema inalador de dose medida e uso do mesmo |
| US6040344A (en) | 1996-11-11 | 2000-03-21 | Sepracor Inc. | Formoterol process |
| WO1999016766A1 (en) | 1997-10-01 | 1999-04-08 | Kyowa Hakko Kogyo Co., Ltd. | Benzodioxole derivatives |
| ATE270278T1 (de) | 1998-03-14 | 2004-07-15 | Altana Pharma Ag | Phthalazinone pde iii/iv hemmer |
| JP2002512183A (ja) | 1998-04-18 | 2002-04-23 | グラクソ グループ リミテッド | 医薬用エアゾール製剤 |
| GB9808802D0 (en) | 1998-04-24 | 1998-06-24 | Glaxo Group Ltd | Pharmaceutical formulations |
| SE9804000D0 (sv) | 1998-11-23 | 1998-11-23 | Astra Ab | New composition of matter |
| US6693202B1 (en) * | 1999-02-16 | 2004-02-17 | Theravance, Inc. | Muscarinic receptor antagonists |
| PT1169019E (pt) | 1999-04-14 | 2003-07-31 | Glaxo Group Ltd | Formulacao farmaceutica em aerossol |
| UA73965C2 (en) | 1999-12-08 | 2005-10-17 | Theravance Inc | b2 ADRENERGIC RECEPTOR ANTAGONISTS |
| GB0103630D0 (en) | 2001-02-14 | 2001-03-28 | Glaxo Group Ltd | Chemical compounds |
| ES2288543T3 (es) | 2001-03-08 | 2008-01-16 | Glaxo Group Limited | Agonistas de beta-adrenorreceptores. |
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| US20030018019A1 (en) * | 2001-06-23 | 2003-01-23 | Boehringer Ingelheim Pharma Kg | Pharmaceutical compositions based on anticholinergics, corticosteroids and betamimetics |
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| PE20050973A1 (es) * | 2003-10-29 | 2005-11-19 | Theravance Inc | Sales de acido naftalen-1,5-disulfonico de un compuesto de 4-amino-1-(piridilmetil)piperidina como antagonistas de receptores muscarinicos |
| TWI341836B (en) | 2004-03-11 | 2011-05-11 | Theravance Inc | Biphenyl compounds useful as muscarinic receptor antagonists |
| TW200540154A (en) * | 2004-06-10 | 2005-12-16 | Theravance Inc | Crystalline form of a substituted pyrrolidine compound |
| WO2006099166A1 (en) * | 2005-03-10 | 2006-09-21 | Theravance, Inc. | Crystalline forms of a biphenyl compound |
| TWI372749B (en) | 2005-03-10 | 2012-09-21 | Theravance Inc | Crystalline forms of a biphenyl compound |
| US7465870B1 (en) * | 2008-03-11 | 2008-12-16 | Homan Randy W | Illuminated heart-shaped guitar with strobe lights and a modified bridge |
| MX2012000682A (es) | 2009-07-15 | 2012-02-28 | Theravance Inc | Formas de bases libres cristalinas de un compuesto de bifenilo. |
| SG186708A1 (en) | 2010-07-13 | 2013-02-28 | Theravance Inc | Process for preparing a biphenyl-2-ylcarbamic acid |
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2010
- 2010-07-14 MX MX2012000682A patent/MX2012000682A/es active IP Right Grant
- 2010-07-14 JP JP2012520734A patent/JP5651174B2/ja active Active
- 2010-07-14 EP EP15178848.6A patent/EP2987490B1/en active Active
- 2010-07-14 ES ES15178848.6T patent/ES2639642T3/es active Active
- 2010-07-14 HU HUE10732616A patent/HUE026414T2/hu unknown
- 2010-07-14 CA CA2989129A patent/CA2989129C/en active Active
- 2010-07-14 US US12/835,964 patent/US8541451B2/en active Active
- 2010-07-14 AU AU2010273514A patent/AU2010273514B2/en active Active
- 2010-07-14 HR HRP20151344TT patent/HRP20151344T1/hr unknown
- 2010-07-14 CA CA2765621A patent/CA2765621C/en active Active
- 2010-07-14 PT PT107326167T patent/PT2453894E/pt unknown
- 2010-07-14 DK DK10732616.7T patent/DK2453894T3/en active
- 2010-07-14 CN CN2010800304581A patent/CN102470130B/zh active Active
- 2010-07-14 BR BR112012000890A patent/BR112012000890A2/pt not_active Application Discontinuation
- 2010-07-14 SG SG10201407913UA patent/SG10201407913UA/en unknown
- 2010-07-14 ES ES10732616.7T patent/ES2557553T3/es active Active
- 2010-07-14 EP EP10732616.7A patent/EP2453894B1/en active Active
- 2010-07-14 PL PL10732616T patent/PL2453894T3/pl unknown
- 2010-07-14 KR KR1020127004005A patent/KR101742252B1/ko active Active
- 2010-07-14 PL PL15178848T patent/PL2987490T3/pl unknown
- 2010-07-14 SG SG2012003067A patent/SG178036A1/en unknown
- 2010-07-14 WO PCT/US2010/041903 patent/WO2011008809A1/en not_active Ceased
- 2010-07-14 SI SI201031095T patent/SI2453894T1/sl unknown
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2011
- 2011-12-15 IL IL216995A patent/IL216995A/en active IP Right Grant
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2013
- 2013-08-22 US US13/973,174 patent/US8921396B2/en active Active
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2014
- 2014-10-07 JP JP2014206123A patent/JP6338505B2/ja active Active
- 2014-11-19 US US14/547,455 patent/US9226896B2/en active Active
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2015
- 2015-11-04 JP JP2015216372A patent/JP2016026214A/ja active Pending
- 2015-12-01 US US14/955,515 patent/US9415041B2/en active Active
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2016
- 2016-01-20 SM SM201600019T patent/SMT201600019B/it unknown
- 2016-07-11 US US15/206,877 patent/US9765028B2/en active Active
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2017
- 2017-07-10 JP JP2017134632A patent/JP2017171692A/ja active Pending
- 2017-08-15 US US15/677,264 patent/US10100013B2/en active Active
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2018
- 2018-09-13 US US16/130,079 patent/US10550081B2/en active Active
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2019
- 2019-12-16 US US16/715,225 patent/US11008289B2/en active Active
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2021
- 2021-04-15 US US17/301,820 patent/US11691948B2/en active Active
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2022
- 2022-06-15 US US17/841,567 patent/US11649209B2/en active Active
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2023
- 2023-05-19 US US18/199,812 patent/US11858898B2/en active Active
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2024
- 2024-07-02 US US18/762,102 patent/US20250179019A1/en active Pending
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