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RU2019120680A - Фармацевтическая композиция для лечения опухоли - Google Patents

Фармацевтическая композиция для лечения опухоли Download PDF

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RU2019120680A
RU2019120680A RU2019120680A RU2019120680A RU2019120680A RU 2019120680 A RU2019120680 A RU 2019120680A RU 2019120680 A RU2019120680 A RU 2019120680A RU 2019120680 A RU2019120680 A RU 2019120680A RU 2019120680 A RU2019120680 A RU 2019120680A
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pharmaceutical composition
tumor
lenvatinib
pharmaceutically acceptable
acceptable salt
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RU2019120680A
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RU2750539C2 (ru
RU2019120680A3 (ru
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Йоити ОДЗАВА
Юсаку ХОРИ
Кадзухико ЯМАДА
Хироси КАМИЯМА
Масахиро МАЦУКИ
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Эйсай Ар Энд Ди Менеджмент Ко., Лтд.
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

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  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Claims (23)

1. Фармацевтическая композиция для лечения опухоли, содержащая (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамид, где (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамид вводят в комбинации с ленватинибом или его фармацевтически приемлемой солью.
2. Фармацевтическая композиция для лечения опухоли, содержащая ленватиниб или его фармацевтически приемлемую соль, где ленватиниб или его фармацевтически приемлемую соль вводят в комбинации с (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамидом.
3. Фармацевтическая композиция по п. 1 или 2, где ленватиниб или его фармацевтически приемлемая соль представляет собой ленватиниба мезилат.
4. Фармацевтическая композиция по любому из пп. 1–3, дополнительно содержащая вспомогательное вещество.
5. Фармацевтическая композиция по любому из пп. 1–4, где ленватиниб или его фармацевтически приемлемая соль и (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамид вводят одновременно, по отдельности, непрерывно или через определенные интервалы времени.
6. Фармацевтическая композиция по любому из пп. 1–5, где опухоль представляет собой рак молочной железы, рак щитовидной железы, гепатоцеллюлярную карциному, колоректальный рак, почечноклеточную карциному, рак головы и шеи, рак эндометрия или меланому.
7. Фармацевтическая композиция по п. 6, где опухоль представляет собой рак молочной железы.
8. Фармацевтическая композиция по п. 6, где опухоль представляет собой рак щитовидной железы.
9. Фармацевтическая композиция по п. 8, где рак щитовидной железы представляет собой анапластический рак щитовидной железы.
10. Фармацевтическая композиция по п. 6, где опухоль представляет собой гепатоцеллюлярную карциному.
11. Фармацевтическая композиция по п. 6, где опухоль представляет собой колоректальный рак.
12. Фармацевтическая композиция по п. 6, где опухоль представляет собой почечноклеточную карциному.
13. Фармацевтическая композиция по п. 6, где опухоль представляет собой рак головы и шеи.
14. Фармацевтическая композиция по п. 6, где опухоль представляет собой рак эндометрия.
15. Фармацевтическая композиция по п. 6, где опухоль представляет собой меланому.
16. Терапевтическое средство для лечения опухоли, содержащее (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамид, где (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамид вводят в комбинации с ленватинибом или его фармацевтически приемлемой солью.
17. Терапевтическое средство для лечения опухоли, содержащее ленватиниб или его фармацевтически приемлемую соль, где ленватиниб или его фармацевтически приемлемую соль вводят в комбинации с (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамидом.
18. Способ лечения опухоли, включающий введение ленватиниба или его фармацевтически приемлемой соли и (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамида нуждающемуся в этом пациенту.
19. Применение (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамида для получения фармацевтической композиции для лечения опухоли, где (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамид вводят в комбинации с ленватинибом или его фармацевтически приемлемой солью.
20. Применение ленватиниба или его фармацевтически приемлемой соли с целью получения фармацевтической композиции для лечения опухоли, где ленватиниб или его фармацевтически приемлемую соль вводят в комбинации с (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамидом.
21. (6S,9aS)–N–Бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамид для применения в лечении опухоли в комбинации с ленватинибом или его фармацевтически приемлемой солью.
22. Ленватиниб или его фармацевтически приемлемая соль для применения в лечении опухоли в комбинации с (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамидом.
23. Фармацевтическая композиция для лечения опухоли, содержащая ленватиниб или его фармацевтически приемлемую соль и (6S,9aS)–N–бензил–8–({6–[3–(4–этилпиперазин–1–ил)азетидин–1–ил]пиридин–2–ил}метил)–6–(2–фтор–4–гидроксибензил)–4,7–диоксо–2–(проп–2–ен–1–ил)гексагидро–2H–пиразино[2,1–c][1,2,4]триазин–1(6H)–карбоксамид.
RU2019120680A 2017-02-08 2018-02-06 Фармацевтическая композиция для лечения опухоли RU2750539C2 (ru)

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PCT/JP2018/004007 WO2018147275A1 (ja) 2017-02-08 2018-02-06 腫瘍治療用医薬組成物

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