MX2021005011A - Métodos de tratamiento del cáncer en pacientes identificados por biomarcadores con inhibidores no covalentes de cinasa 7 dependiente de ciclina (cdk7). - Google Patents

Métodos de tratamiento del cáncer en pacientes identificados por biomarcadores con inhibidores no covalentes de cinasa 7 dependiente de ciclina (cdk7).

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Publication number
MX2021005011A
MX2021005011A MX2021005011A MX2021005011A MX2021005011A MX 2021005011 A MX2021005011 A MX 2021005011A MX 2021005011 A MX2021005011 A MX 2021005011A MX 2021005011 A MX2021005011 A MX 2021005011A MX 2021005011 A MX2021005011 A MX 2021005011A
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Mexico
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methods
cdk7
identified
cyclin
biomarker
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MX2021005011A
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English (en)
Inventor
Liv Helena Johannessen
John Graeme Hodgson
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Syros Pharmaceuticals Inc
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Publication of MX2021005011A publication Critical patent/MX2021005011A/es

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    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C07F9/65583Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
    • AHUMAN NECESSITIES
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non 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
    • AHUMAN NECESSITIES
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
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    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/56Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/565Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
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    • A61K47/26Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
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    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
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    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
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    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled

Abstract

La presente invención se refiere a métodos para identificar pacientes que padezcan varios tipos de cáncer que tengan más probabilidades de responder al tratamiento con un inhibidor de CDK7 conforme a la Fórmula estructural (I), (Ia), una especie del mismo o una forma específica del mismo (tal como descrito en el presente documento), ya sea cuando se administre o se use solo o en combinación con un segundo agente terapéutico (por ejemplo, otra terapia contra el cáncer). Los pacientes se identifican en función de una o más características (por ejemplo, número de copias de genes o nivel de expresión) de ciertos biomarcadores (por ejemplo, RB1 u otro miembro de la vía de E2F). Además, la presente invención se refiere a métodos para tratar a un paciente identificado con un compuesto que se ajusta a la Fórmula estructural (I), (Ia), una especie del mismo o una forma específica del mismo, ya sea solo o en combinación con un segundo agente terapéutico. En otro aspecto, la presente invención presenta kits que incluyen instrucciones para tratar a un paciente identificado como se describe en el presente documento.
MX2021005011A 2018-11-01 2019-11-01 Métodos de tratamiento del cáncer en pacientes identificados por biomarcadores con inhibidores no covalentes de cinasa 7 dependiente de ciclina (cdk7). MX2021005011A (es)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201862754398P 2018-11-01 2018-11-01
US201962877189P 2019-07-22 2019-07-22
US201962915983P 2019-10-16 2019-10-16
US201962927469P 2019-10-29 2019-10-29
PCT/US2019/059535 WO2020093006A1 (en) 2018-11-01 2019-11-01 Methods of treating cancer in biomarker-identified patients with non-covalent inhibitors of cyclin-dependent kinase 7 (cdk7)

Publications (1)

Publication Number Publication Date
MX2021005011A true MX2021005011A (es) 2021-07-21

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Family Applications (2)

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MX2021005007A MX2021005007A (es) 2018-11-01 2019-11-01 Inhibidores de cinasa 7 dependiente de ciclina (cdk7).
MX2021005011A MX2021005011A (es) 2018-11-01 2019-11-01 Métodos de tratamiento del cáncer en pacientes identificados por biomarcadores con inhibidores no covalentes de cinasa 7 dependiente de ciclina (cdk7).

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MX2021005007A MX2021005007A (es) 2018-11-01 2019-11-01 Inhibidores de cinasa 7 dependiente de ciclina (cdk7).

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US (3) US20210401859A1 (es)
EP (2) EP3873462A4 (es)
JP (2) JP2022508055A (es)
KR (1) KR20210118812A (es)
CN (2) CN113226306A (es)
AU (2) AU2019371454A1 (es)
BR (1) BR112021008516A2 (es)
CA (2) CA3118330A1 (es)
CO (1) CO2021007230A2 (es)
CR (1) CR20210287A (es)
IL (1) IL282737A (es)
MX (2) MX2021005007A (es)
PH (1) PH12021550995A1 (es)
SG (1) SG11202104438VA (es)
WO (2) WO2020093011A1 (es)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110036004A (zh) * 2016-07-13 2019-07-19 希洛斯医药品股份有限公司 细胞周期蛋白依赖性激酶7(cdk7)的抑制剂
WO2019143719A1 (en) 2018-01-16 2019-07-25 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
EP3740206B1 (en) 2018-01-16 2024-03-06 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
CA3118330A1 (en) * 2018-11-01 2020-05-07 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
IL292519A (en) * 2019-10-29 2022-06-01 Syros Pharmaceuticals Inc Methods for treating cancer in patients identified with a biomarker with cyclin-dependent kinase 7 (cdk7) inhibitors
AU2021280351A1 (en) * 2020-05-29 2023-01-05 Syros Pharmaceuticals, Inc. Methods of treating cancer in patients with an anomalous KRAS gene or deletions within chromosome 9
CN112661745A (zh) 2020-07-24 2021-04-16 浙江同源康医药股份有限公司 用作cdk7激酶抑制剂的化合物及其应用
WO2022063212A1 (zh) * 2020-09-24 2022-03-31 广州费米子科技有限责任公司 嘧啶基衍生物、其制备方法及其用途
EP4229038A1 (en) * 2020-10-16 2023-08-23 Syros Pharmaceuticals, Inc. Dosing regimens for cyclin-dependent kinase 7 (cdk7) inhibitors
WO2022089444A1 (zh) * 2020-10-28 2022-05-05 恒元生物医药科技(苏州)有限公司 一种含氮杂环化合物及其应用
JP2024501833A (ja) 2020-12-24 2024-01-16 ジーティー アペイロン セラピューティクス リミテッド 芳香族複素環式化合物、並びにその薬学的組成物及び用途
EP4319744A1 (en) * 2021-04-10 2024-02-14 MEI Pharma, Inc. Voruciclib dosing regimens and methods of treatment including the same
WO2023014817A1 (en) * 2021-08-03 2023-02-09 Syros Pharmaceuticals, Inc. Compositions and methods for treating lymphomas with a cdk7 inhibitor in combination with a btk inhibitor
WO2023040998A1 (en) * 2021-09-17 2023-03-23 Taizhou Eoc Pharma Co., Ltd. A cyclin-dependent kinase inhibitor
WO2023049691A1 (en) * 2021-09-23 2023-03-30 Zeno Management, Inc. Cdk7 inhibitors and methods of treating cancer
WO2023109876A1 (en) * 2021-12-16 2023-06-22 Edigene Therapeutics (Beijing) Inc. Biomarkers for colorectal cancer treatment
TW202340211A (zh) * 2021-12-22 2023-10-16 香港商英矽智能科技知識產權有限公司 嘧啶雜環化合物、其製法與醫藥上的用途
US11945785B2 (en) 2021-12-30 2024-04-02 Biomea Fusion, Inc. Pyrazine compounds as inhibitors of FLT3
CN114736204A (zh) * 2022-05-06 2022-07-12 湖北工业大学 一种培西达替尼结构类似物的制备方法及其抗肿瘤中的应用
WO2023246371A1 (zh) * 2022-06-24 2023-12-28 中国科学院基础医学与肿瘤研究所(筹) 具有嘧啶并噻吩结构的小分子化合物及其应用
CN117384135A (zh) * 2022-07-04 2024-01-12 浙江同源康医药股份有限公司 用作cdk7激酶抑制剂的化合物及其应用
CN116082337B (zh) * 2023-03-16 2023-06-23 英矽智能科技(上海)有限公司 炔基取代的杂环化合物,其制法与医药上的用途

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7351834B1 (en) 1999-01-13 2008-04-01 Bayer Pharmaceuticals Corporation ω-Carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
EP2298311B1 (en) 1999-01-13 2012-05-09 Bayer HealthCare LLC w-Carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors
WO2001026147A1 (fr) 1999-10-04 2001-04-12 Seiko Epson Corporation Dispositif a semi-conducteur, son procede de fabrication, carte de circuit imprime et dispositif electronique
GB0000313D0 (en) 2000-01-10 2000-03-01 Astrazeneca Uk Ltd Formulation
US7235576B1 (en) 2001-01-12 2007-06-26 Bayer Pharmaceuticals Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
IL161156A0 (en) 2001-10-30 2004-08-31 Novartis Ag Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity
MXPA04007832A (es) 2002-02-11 2005-09-08 Bayer Pharmaceuticals Corp Aril-ureas con actividad inhibitoria de angiogenesis.
GB0308466D0 (en) * 2003-04-11 2003-05-21 Novartis Ag Organic compounds
TWI324604B (en) 2003-06-18 2010-05-11 Novartis Ag New use of staurosporine derivatives
SG155996A1 (en) 2004-09-29 2009-10-29 Bayer Schering Pharma Ag Thermodynamically stable form of bay 43-9006 tosylate
WO2006038001A1 (en) * 2004-10-06 2006-04-13 Celltech R & D Limited Aminopyrimidine derivatives as jnk inhibitors
AU2006220809B2 (en) 2005-03-04 2009-06-11 Merck Sharp & Dohme Corp. Fused aromatic compounds having anti-diabetic activity
SG160364A1 (en) 2005-03-07 2010-04-29 Bayer Schering Pharma Ag Pharmaceutical composition comprising an omega-carboxyaryl substituted diphenyl urea for the treatment of cancer
ES2761180T3 (es) 2005-12-23 2020-05-19 Ariad Pharma Inc Compuestos bicíclicos de heteroarilo
US8338458B2 (en) 2007-05-07 2012-12-25 Merck Sharp & Dohme Corp. Method of treatment using fused aromatic compounds having anti-diabetic activity
EP2239264A4 (en) 2007-12-28 2012-01-11 Mitsubishi Tanabe Pharma Corp ANTITUMOR AGENT
CA2723961C (en) * 2008-05-21 2017-03-21 Ariad Pharmaceuticals, Inc. Phosphorous derivatives as kinase inhibitors
US8546399B2 (en) 2009-05-26 2013-10-01 Abbvie Inc. Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases
US8563567B2 (en) 2009-12-30 2013-10-22 Arqule, Inc. Substituted heterocyclic compounds
MX2013006467A (es) 2010-12-09 2013-10-01 Amgen Inc Compuestos biciclicos como inhibidores pim.
KR20200110711A (ko) 2012-09-07 2020-09-24 제넨테크, 인크. Ii형 항-cd20 항체와 선택적 bcl-2 억제제와의 병용 치료요법
US20140296218A1 (en) 2012-10-25 2014-10-02 Whitehead Institute For Biomedical Research Super-enhancers and methods of use thereof
CA3022250A1 (en) 2012-12-12 2014-06-12 Ariad Pharmaceuticals, Inc. Crystalline forms of 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide mono hydrochloride
US9145387B2 (en) 2013-02-08 2015-09-29 Celgene Avilomics Research, Inc. ERK inhibitors and uses thereof
ES2676734T3 (es) * 2013-10-18 2018-07-24 Syros Pharmaceuticals, Inc. Compuestos heteroatómicos útiles para el tratamiento de enfermedades proliferativas
JP6491202B2 (ja) * 2013-10-18 2019-03-27 デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド サイクリン依存性キナーゼ7(cdk7)の多環阻害剤
WO2015058163A2 (en) * 2013-10-18 2015-04-23 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
CN106458990B (zh) * 2014-04-04 2019-06-07 希洛斯医药品股份有限公司 细胞周期蛋白依赖性激酶7(cdk7)的抑制剂
EP3805218A1 (en) * 2014-04-05 2021-04-14 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
CN106660993B (zh) 2014-06-12 2020-09-11 上海复尚慧创医药研究有限公司 一类激酶抑制剂
SI3157916T1 (sl) 2014-06-19 2019-05-31 Ariad Pharmaceuticals, Inc. Heteroarilne spojine za zaviranja kinaze
WO2016058544A1 (en) * 2014-10-16 2016-04-21 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
CA2978518C (en) 2015-03-27 2023-11-21 Nathanael S. Gray Inhibitors of cyclin-dependent kinases
SG11201805092WA (en) * 2015-12-23 2018-07-30 Harvard College Cortistatin analogs and uses thereof
CN110036004A (zh) * 2016-07-13 2019-07-19 希洛斯医药品股份有限公司 细胞周期蛋白依赖性激酶7(cdk7)的抑制剂
WO2018098473A1 (en) 2016-11-28 2018-05-31 Dana-Farber Cancer Institute, Inc. Reagents and methods for analysis of proteins and metabolites targeted by covalent probes
CN117343049A (zh) 2017-06-30 2024-01-05 北京泰德制药股份有限公司 Rho相关蛋白激酶抑制剂、包含其的药物组合物及其制备方法和用途
WO2019143719A1 (en) 2018-01-16 2019-07-25 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
EP3740206B1 (en) * 2018-01-16 2024-03-06 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
WO2019204781A1 (en) 2018-04-20 2019-10-24 Design Therapeutics Inc. Methods and compounds for the treatment of genetic disease
EP4234553A3 (en) 2018-05-09 2023-09-06 Design Therapeutics, Inc. Methods and compounds for the treatment of genetic disease
CA3118330A1 (en) * 2018-11-01 2020-05-07 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
AU2021280351A1 (en) * 2020-05-29 2023-01-05 Syros Pharmaceuticals, Inc. Methods of treating cancer in patients with an anomalous KRAS gene or deletions within chromosome 9

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JP2022515705A (ja) 2022-02-22
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KR20210118812A (ko) 2021-10-01
US20200190126A1 (en) 2020-06-18
CN113226306A (zh) 2021-08-06
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US20210403495A1 (en) 2021-12-30
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AU2019371454A1 (en) 2021-05-27
US10738067B2 (en) 2020-08-11
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JP2022508055A (ja) 2022-01-19
WO2020093006A8 (en) 2022-01-06
US20210401859A1 (en) 2021-12-30
CA3118330A1 (en) 2020-05-07
PH12021550995A1 (en) 2021-10-04
MX2021005007A (es) 2021-07-21
CO2021007230A2 (es) 2021-10-29
AU2019374142A1 (en) 2021-05-27
BR112021008516A2 (pt) 2021-09-14
CR20210287A (es) 2022-02-15

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