RU2011138835A - Применение производного рапамицина - Google Patents

Применение производного рапамицина Download PDF

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RU2011138835A
RU2011138835A RU2011138835/15A RU2011138835A RU2011138835A RU 2011138835 A RU2011138835 A RU 2011138835A RU 2011138835/15 A RU2011138835/15 A RU 2011138835/15A RU 2011138835 A RU2011138835 A RU 2011138835A RU 2011138835 A RU2011138835 A RU 2011138835A
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Russia
Prior art keywords
ramapicin
derivative
application
rapamycin
hydroxyethyl
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RU2011138835/15A
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English (en)
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RU2483727C1 (ru
Inventor
Хейди ЛАНЕ
Теренс О'РЕЙЛЛИ
Джинетта Марджори ВУД
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Новартис Аг
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26245731&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=RU2011138835(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from GB0104072A external-priority patent/GB0104072D0/en
Priority claimed from GB0124957A external-priority patent/GB0124957D0/en
Application filed by Новартис Аг filed Critical Новартис Аг
Publication of RU2011138835A publication Critical patent/RU2011138835A/ru
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    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/436Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
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Abstract

1. Применение 40-O-(2-гидроксиэтил)-рапамицина для получения фармацевтической композиции, предназначенной для лечения опухоли поджелудочной железы.2. Применение по п.1, где единичная доза 40-O-(2-гидроксиэтил)-рапамицина, составляющая от 0, 1 до 25 мг, вводится ежедневно.3. Применение по любому из пп.1 или 2, дополнительно включающее один или более фармацевтически приемлемый растворитель или носитель.

Claims (3)

1. Применение 40-O-(2-гидроксиэтил)-рапамицина для получения фармацевтической композиции, предназначенной для лечения опухоли поджелудочной железы.
2. Применение по п.1, где единичная доза 40-O-(2-гидроксиэтил)-рапамицина, составляющая от 0, 1 до 25 мг, вводится ежедневно.
3. Применение по любому из пп.1 или 2, дополнительно включающее один или более фармацевтически приемлемый растворитель или носитель.
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