IL261721B - Combinations of lsd1 inhibitors for use in the treatment of solid tumors - Google Patents
Combinations of lsd1 inhibitors for use in the treatment of solid tumorsInfo
- Publication number
- IL261721B IL261721B IL261721A IL26172118A IL261721B IL 261721 B IL261721 B IL 261721B IL 261721 A IL261721 A IL 261721A IL 26172118 A IL26172118 A IL 26172118A IL 261721 B IL261721 B IL 261721B
- Authority
- IL
- Israel
- Prior art keywords
- cancer
- pharmaceutically acceptable
- acceptable salt
- inhibitor
- diamine
- Prior art date
Links
Classifications
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- 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
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
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- A—HUMAN NECESSITIES
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- A61K31/12—Ketones
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- A—HUMAN NECESSITIES
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- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
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- A61K31/282—Platinum compounds
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- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
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- 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
- A61K31/4402—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 2, e.g. pheniramine, bisacodyl
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- 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
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- A61K31/47—Quinolines; Isoquinolines
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- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/475—Quinolines; Isoquinolines having an indole ring, e.g. yohimbine, reserpine, strychnine, vinblastine
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- 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
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/52—Purines, e.g. adenine
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
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- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
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- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
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- A61K31/7068—Compounds 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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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pain & Pain Management (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Inorganic Chemistry (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662308529P | 2016-03-15 | 2016-03-15 | |
| PCT/EP2017/055784 WO2017157825A1 (en) | 2016-03-15 | 2017-03-13 | Combinations of lsd1 inhibitors for use in the treatment of solid tumors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL261721A IL261721A (en) | 2018-10-31 |
| IL261721B true IL261721B (en) | 2022-07-01 |
Family
ID=58266657
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL261721A IL261721B (en) | 2016-03-15 | 2017-03-13 | Combinations of lsd1 inhibitors for use in the treatment of solid tumors |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US10265279B2 (enExample) |
| EP (1) | EP3429571B1 (enExample) |
| JP (2) | JP7158023B2 (enExample) |
| KR (2) | KR102511024B1 (enExample) |
| CN (2) | CN120661674A (enExample) |
| AR (1) | AR107871A1 (enExample) |
| AU (2) | AU2017233898B2 (enExample) |
| CA (1) | CA3017411C (enExample) |
| EA (1) | EA201892075A1 (enExample) |
| IL (1) | IL261721B (enExample) |
| MX (2) | MX381890B (enExample) |
| MY (1) | MY199967A (enExample) |
| SG (2) | SG10201913331VA (enExample) |
| WO (1) | WO2017157825A1 (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3736265A1 (en) | 2011-10-20 | 2020-11-11 | Oryzon Genomics, S.A. | (hetero)aryl cyclopropylamine compounds as lsd1 inhibitors |
| EP3090998A1 (en) | 2015-05-06 | 2016-11-09 | F. Hoffmann-La Roche AG | Solid forms |
| EP3307267B1 (en) | 2016-06-10 | 2019-04-10 | Oryzon Genomics, S.A. | Multiple sclerosis treatment |
| AU2017233898B2 (en) | 2016-03-15 | 2022-12-15 | Oryzon Genomics, S.A. | Combinations of LSD1 inhibitors for use in the treatment of solid tumors |
| KR102646126B1 (ko) * | 2016-03-15 | 2024-03-11 | 오리존 지노믹스 에스.에이. | 혈액 악성 종양의 치료를 위한 lsd1 억제제의 조합물 |
| US11685782B2 (en) | 2017-10-23 | 2023-06-27 | Children's Medical Center Corporation | Methods of treating cancer using LSD1 inhibitors in combination with immunotherapy |
| MA50564A (fr) | 2017-11-06 | 2020-09-16 | Hutchinson Fred Cancer Res | Association d'une thérapie cellulaire et d'un inhibiteur de gamma secrétase |
| WO2019108789A1 (en) * | 2017-11-29 | 2019-06-06 | The Trustees Of Columbia University In The City Of New York | Combination therapy of lymphoma |
| KR20210006426A (ko) * | 2018-05-04 | 2021-01-18 | 오리존 지노믹스 에스.에이. | 안정한 약제학적 제제 |
| MX2020011826A (es) | 2018-05-06 | 2021-01-15 | Ayala Pharmaceuticals Inc | Composiciones de combinacion que comprenden compuestos de bisfluoroalquil-1,4-benzodiazepinona y metodos de uso de las mismas. |
| CN109265462B (zh) * | 2018-10-31 | 2020-06-02 | 郑州大学 | 嘧啶并1,2,4-三氮唑类化合物及其制备方法和应用 |
| SG11202109025XA (en) * | 2019-03-25 | 2021-09-29 | Oryzon Genomics Sa | Combinations of iadademstat for cancer therapy |
| JP2022546908A (ja) * | 2019-07-05 | 2022-11-10 | オリゾン・ゲノミクス・ソシエダッド・アノニマ | Kdm1a阻害剤を使用した小細胞肺がんの個別化された処置のためのバイオマーカーおよび方法 |
| CN110863047B (zh) * | 2019-11-15 | 2022-09-13 | 西安交通大学医学院第一附属医院 | 人ccdc154基因的用途及相关产品 |
| WO2021154878A1 (en) | 2020-01-28 | 2021-08-05 | PAIGE.AI, Inc. | Systems and methods for processing electronic images for biomarker localization |
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| WO2021228146A1 (zh) * | 2020-05-12 | 2021-11-18 | 石药集团中奇制药技术(石家庄)有限公司 | 一种lsd1抑制剂的用途 |
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- 2017-03-13 CN CN202510879513.2A patent/CN120661674A/zh active Pending
- 2017-03-13 KR KR1020187029530A patent/KR102511024B1/ko active Active
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- 2017-03-13 JP JP2018548076A patent/JP7158023B2/ja active Active
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2018
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2022
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| WO2013057322A1 (en) * | 2011-10-20 | 2013-04-25 | Oryzon Genomics, S.A. | (hetero)aryl cyclopropylamine compounds as lsd1 inhibitors |
| WO2015134973A1 (en) * | 2014-03-07 | 2015-09-11 | The Johns Hopkins University | Inhibitors of histone lysine specific demethylase (lsd1) and histone deacetylases (hdacs) |
| WO2016025635A2 (en) * | 2014-08-13 | 2016-02-18 | Epizyme, Inc. | Combination therapy for treating cancer |
| CN105233292A (zh) * | 2015-10-19 | 2016-01-13 | 中国科学院北京基因组研究所 | Ory-1001联合放疗和化疗用于治疗人三阴性乳腺癌的用途 |
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| SINGH, MELISSA M., ET AL., PRECLINICAL ACTIVITY OF COMBINED HDAC AND KDM1A INHIBITION IN GLIOBLASTOMA., 19 March 2015 (2015-03-19) * |
Also Published As
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| MX2018011102A (es) | 2019-01-10 |
| CN109195593A (zh) | 2019-01-11 |
| MY199967A (en) | 2023-11-30 |
| AR107871A1 (es) | 2018-06-13 |
| KR20180118229A (ko) | 2018-10-30 |
| SG11201807965YA (en) | 2018-10-30 |
| JP7158023B2 (ja) | 2022-10-21 |
| MX2021004639A (es) | 2022-02-21 |
| AU2017233898B2 (en) | 2022-12-15 |
| KR102511024B1 (ko) | 2023-03-16 |
| CA3017411C (en) | 2024-06-25 |
| JP2019508440A (ja) | 2019-03-28 |
| US20170281567A1 (en) | 2017-10-05 |
| CA3017411A1 (en) | 2017-09-21 |
| SG10201913331VA (en) | 2020-03-30 |
| BR112018068565A2 (pt) | 2019-02-12 |
| JP2023011569A (ja) | 2023-01-24 |
| EP3429571A1 (en) | 2019-01-23 |
| EP3429571B1 (en) | 2025-10-08 |
| CN120661674A (zh) | 2025-09-19 |
| WO2017157825A1 (en) | 2017-09-21 |
| AU2017233898A1 (en) | 2018-11-01 |
| MX381890B (es) | 2025-03-13 |
| KR20230042756A (ko) | 2023-03-29 |
| IL261721A (en) | 2018-10-31 |
| US20220378722A1 (en) | 2022-12-01 |
| US10265279B2 (en) | 2019-04-23 |
| EA201892075A1 (ru) | 2019-04-30 |
| AU2023201580A1 (en) | 2023-04-13 |
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