JP2009545600A5 - - Google Patents
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- JP2009545600A5 JP2009545600A5 JP2009522882A JP2009522882A JP2009545600A5 JP 2009545600 A5 JP2009545600 A5 JP 2009545600A5 JP 2009522882 A JP2009522882 A JP 2009522882A JP 2009522882 A JP2009522882 A JP 2009522882A JP 2009545600 A5 JP2009545600 A5 JP 2009545600A5
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutical composition
- isoindol
- dione
- piperidine
- dihydro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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Claims (16)
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンを含む、ヒトのマントル細胞リンパ腫を治療するための医薬組成物。
- 前記マントル細胞リンパ腫が、再発性、難治性、又は従来の療法に抵抗性である、請求項1記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンが、約1〜約50mg/日の量で投与されるように用いられることを特徴とする、請求項1又は2記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンが、約10、15、20又は25mg/日の量で投与されるように用いられることを特徴とする、請求項3記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンが、約25mg/日の量で投与されるように用いられることを特徴とする、請求項4記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンが、鏡像異性的に純粋である、請求項3記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンが、S鏡像異性体である、請求項6記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンが、R鏡像異性体である、請求項6記載の医薬組成物。
- 経口投与用に製剤されている、請求項3記載の医薬組成物。
- カプセル又は錠剤の形態である、請求項9記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンが、28日のサイクルにおいて、21日間投与され、続いて7日間休薬されるように用いられることを特徴とする、請求項3記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンが、28日のサイクルにおいて、約25mg/日の量で21日間投与され、続いて7日間休薬されるように用いられることを特徴とする、請求項11記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンとともに又は別々に、リツキシマブが毎週静脈内注射によって375mg/m2の量で投与されるように用いられることを特徴とする、請求項12記載の医薬組成物。
- 3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンを含む、マントル細胞リンパ腫を治療するための医薬組成物であって、3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンとともに又は別々に、第2の活性薬剤が投与されるように用いられることを特徴とする、前記医薬組成物。
- 前記第2の活性薬剤が、抗体、造血成長因子、サイトカイン、抗癌剤、抗生物質、cox-2阻害剤、免疫調節剤、免疫抑制剤、コルチコステロイド又は薬理活性変異体、或いはそれらの誘導体である、請求項14記載の医薬組成物。
- 前記第2の活性薬剤が、リツキシマブである、請求項14記載の医薬組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83575206P | 2006-08-03 | 2006-08-03 | |
US60/835,752 | 2006-08-03 | ||
PCT/US2007/017343 WO2008019065A1 (en) | 2006-08-03 | 2007-08-02 | Use of 3- (4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for the treatment of mantle cell lymphomas |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013168932A Division JP2013256514A (ja) | 2006-08-03 | 2013-08-15 | マントル細胞リンパ腫治療のための3−(4−アミノ−1−オキソ−1,3−ジヒドロ−イソインドール−2−イル)−ピペリジン−2,6−ジオンの使用 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2009545600A JP2009545600A (ja) | 2009-12-24 |
JP2009545600A5 true JP2009545600A5 (ja) | 2010-09-02 |
JP5465005B2 JP5465005B2 (ja) | 2014-04-09 |
Family
ID=38691762
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009522882A Active JP5465005B2 (ja) | 2006-08-03 | 2007-08-02 | マントル細胞リンパ腫治療のための3−(4−アミノ−1−オキソ−1,3−ジヒドロ−イソインドール−2−イル)−ピペリジン−2,6−ジオンの使用 |
JP2013168932A Withdrawn JP2013256514A (ja) | 2006-08-03 | 2013-08-15 | マントル細胞リンパ腫治療のための3−(4−アミノ−1−オキソ−1,3−ジヒドロ−イソインドール−2−イル)−ピペリジン−2,6−ジオンの使用 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013168932A Withdrawn JP2013256514A (ja) | 2006-08-03 | 2013-08-15 | マントル細胞リンパ腫治療のための3−(4−アミノ−1−オキソ−1,3−ジヒドロ−イソインドール−2−イル)−ピペリジン−2,6−ジオンの使用 |
Country Status (26)
Country | Link |
---|---|
US (7) | US20080038263A1 (ja) |
EP (1) | EP2046331B1 (ja) |
JP (2) | JP5465005B2 (ja) |
KR (2) | KR20140082859A (ja) |
CN (2) | CN102908346A (ja) |
AR (1) | AR062265A1 (ja) |
AT (1) | ATE486601T1 (ja) |
AU (1) | AU2007282027B2 (ja) |
CA (2) | CA2659774C (ja) |
CL (1) | CL2007002218A1 (ja) |
CY (1) | CY1110989T1 (ja) |
DE (1) | DE602007010303D1 (ja) |
DK (1) | DK2046331T3 (ja) |
ES (1) | ES2351069T3 (ja) |
HR (1) | HRP20100664T1 (ja) |
IL (1) | IL196885A (ja) |
ME (1) | ME01937B (ja) |
MX (1) | MX2009001268A (ja) |
PE (1) | PE20081311A1 (ja) |
PL (1) | PL2046331T3 (ja) |
PT (1) | PT2046331E (ja) |
RS (1) | RS51567B (ja) |
RU (1) | RU2446804C2 (ja) |
SI (1) | SI2046331T1 (ja) |
TW (1) | TWI430797B (ja) |
WO (1) | WO2008019065A1 (ja) |
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EA201071058A1 (ru) * | 2008-03-11 | 2011-02-28 | Др. Редди'С Лабораторис Лтд. | Получение леналидомида |
US20110280913A1 (en) * | 2008-07-31 | 2011-11-17 | The Ohio State University | Methods and Compositions for Delivering Therapeutic Agents in the Treatment of B-Cell Related Disorders |
CN103068386A (zh) * | 2010-03-12 | 2013-04-24 | 细胞基因公司 | 使用来那度胺治疗非霍奇金淋巴瘤的方法及作为预测因子的基因和蛋白质生物标记 |
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CN104004056B (zh) * | 2014-06-23 | 2016-08-17 | 王方杰 | 一种关于Cyclin D蛋白抑制剂多肽及其应用 |
CN104004060B (zh) * | 2014-06-23 | 2016-04-13 | 重庆医科大学 | Cyclin D蛋白抑制剂多肽及其应用 |
CN104031122B (zh) * | 2014-06-23 | 2016-05-11 | 常州市肿瘤医院 | 有关Cyclin D蛋白抑制剂多肽及其应用 |
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US11584733B2 (en) | 2017-01-09 | 2023-02-21 | Shuttle Pharmaceuticals, Inc. | Selective histone deacetylase inhibitors for the treatment of human disease |
CN111372585A (zh) | 2017-11-16 | 2020-07-03 | C4医药公司 | 用于靶蛋白降解的降解剂和降解决定子 |
US10537585B2 (en) | 2017-12-18 | 2020-01-21 | Dexcel Pharma Technologies Ltd. | Compositions comprising dexamethasone |
ES2983284T3 (es) | 2018-01-09 | 2024-10-22 | Shuttle Pharmaceuticals Inc | Inhibidores selectivos de histona deacetilasa para el tratamiento de enfermedades humanas |
CN111902141A (zh) | 2018-03-26 | 2020-11-06 | C4医药公司 | 用于ikaros降解的羟脑苷脂结合剂 |
CN112312904B (zh) | 2018-04-16 | 2025-01-07 | C4医药公司 | 螺环化合物 |
EP3578561A1 (en) | 2018-06-04 | 2019-12-11 | F. Hoffmann-La Roche AG | Spiro compounds |
EP3846800A4 (en) | 2018-09-04 | 2022-08-24 | C4 Therapeutics, Inc. | Compounds for the degradation of brd9 or mth1 |
EP3897631A4 (en) | 2018-12-20 | 2022-11-23 | C4 Therapeutics, Inc. | TARGETED PROTEIN DEGRADATION |
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JP2023538517A (ja) | 2020-08-05 | 2023-09-08 | シーフォー セラピューティクス, インコーポレイテッド | Retの標的分解のための化合物 |
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2007
- 2007-07-31 CL CL200702218A patent/CL2007002218A1/es unknown
- 2007-08-01 TW TW096128250A patent/TWI430797B/zh active
- 2007-08-01 US US11/888,881 patent/US20080038263A1/en not_active Abandoned
- 2007-08-02 CA CA2659774A patent/CA2659774C/en active Active
- 2007-08-02 SI SI200730446T patent/SI2046331T1/sl unknown
- 2007-08-02 CA CA2836006A patent/CA2836006A1/en not_active Abandoned
- 2007-08-02 RS RS20100541A patent/RS51567B/en unknown
- 2007-08-02 AT AT07811048T patent/ATE486601T1/de active
- 2007-08-02 CN CN2012103235264A patent/CN102908346A/zh active Pending
- 2007-08-02 ME MEP-2010-541A patent/ME01937B/me unknown
- 2007-08-02 KR KR1020147014837A patent/KR20140082859A/ko not_active Ceased
- 2007-08-02 EP EP07811048A patent/EP2046331B1/en active Active
- 2007-08-02 ES ES07811048T patent/ES2351069T3/es active Active
- 2007-08-02 CN CN200780036550.7A patent/CN101583359B/zh active Active
- 2007-08-02 JP JP2009522882A patent/JP5465005B2/ja active Active
- 2007-08-02 RU RU2009107535/15A patent/RU2446804C2/ru not_active IP Right Cessation
- 2007-08-02 DE DE602007010303T patent/DE602007010303D1/de active Active
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- 2007-08-02 DK DK07811048.3T patent/DK2046331T3/da active
- 2007-08-02 PT PT07811048T patent/PT2046331E/pt unknown
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- 2007-08-02 WO PCT/US2007/017343 patent/WO2008019065A1/en active Application Filing
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2009
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2014
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2018
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2019
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