JP2001247459A5 - - Google Patents

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JP2001247459A5
JP2001247459A5 JP2000232871A JP2000232871A JP2001247459A5 JP 2001247459 A5 JP2001247459 A5 JP 2001247459A5 JP 2000232871 A JP2000232871 A JP 2000232871A JP 2000232871 A JP2000232871 A JP 2000232871A JP 2001247459 A5 JP2001247459 A5 JP 2001247459A5
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JP2000232871A
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【特許請求の範囲】
【請求項1】 癌の治療方法において、そのような治療を必要とする哺乳類に、同時にまたは連続的に、(i)パクリタキセル(paclitaxel)およびドセタキセル(docetaxel) から選ばれる化合物と、(ii)下記式の化合物
【化1】
Figure 2001247459
(式中、R、RおよびRは、H、C〜Cアルキル、ハロゲン、CF、CN、NO、NH、OH、OR、NHCOR、NHSOR、SR、SORおよびNHRから成る群からそれぞれ独立に選ばれ、各Rは独立に、ヒドロキシ、アミノおよびメトキシから選ばれる1つ以上の置換基で場合によっては置換されたC〜Cアルキルであり、R、RおよびRのそれぞれは、1〜8位の使用できるどの位置に存在してもよく;
かつ式(I)の炭素環式芳香環のそれぞれにおいて、メチン(−CH=)基の2つまでがアザ(−N=)基で置換されてもよく;
かつR、RおよびRのいずれか2つは付加的に一緒に結合して−CH=CH−CH=CH−基を表わしてもよく、この基は、それが結合している炭素または窒素原子と共に縮合六員芳香環を形成してもよい)
またはその薬学的に許容し得る塩もしくはエステルとを投与する段階を含む方法。
【請求項2】 哺乳類がヒトである、請求項1記載の方法。
【請求項3】 式(I)の化合物が下記式の化合物
【化2】
Figure 2001247459
またはその薬学的に許容し得る塩もしくはエステルである、請求項1または2記載の方法。
【請求項4】 式(Ia)の化合物が、5,6−ジメチルキサンテノン−4−酢酸またはその薬学的に許容し得る塩もしくはエステルである、請求項3記載の方法。
【請求項5】 薬剤の製造における請求項1記載の式(I)の化合物またはその薬学的に許容し得る塩もしくはエステルの使用であって、該薬剤は、該薬剤と、パクリタキセルおよびドセタキセルから選ばれる化合物とを連続的にまたは同時に共投与することにより哺乳類の癌を治療するためのものである、使用。
【請求項6】 薬剤の製造におけるドセタキセルおよびパクリタキセルから選ばれる化合物の使用であって、該薬剤は、該薬剤と、請求項1記載の式(I)の化合物またはその薬学的に許容し得る塩もしくはエステルとを連続的にまたは同時に共投与することにより哺乳類の癌を治療するためのものである、使用。
【請求項7】 1つ以上の薬学的に許容し得る担体または賦形剤との組み合わせで、請求項1記載の式(I)の化合物またはその薬学的に許容し得る塩もしくはエステルと、パクリタキセルおよびドセタキセルから選ばれる化合物とを含む、癌を治療するのに適した薬剤組成物。
他の面において、本発明は、薬剤の製造における上に定義した式(I)の化合物またはその薬学的に許容し得る塩もしくはエステルの使用であって、該薬剤は、該薬剤と、パクリタキセルおよびドセタキセルから選ばれる化合物とを連続的にまたは同時に共投与(co-administration)することにより哺乳類の癌を治療するためのものである、使用を提供する。
更に他の面において、本発明は、薬剤の製造におけるドセタキセルおよびパクリタキセルから選ばれる化合物の使用であって、該薬剤は、該薬剤と、上記に定義した式(I)の化合物またはその薬学的に許容し得る塩もしくはエステルとを連続的にまたは同時に共投与することにより哺乳類の癌を治療するためのものである、使用を提供する。


JP2000232871A 2000-03-03 2000-08-01 癌の組み合わせ療法 Pending JP2001247459A (ja)

Applications Claiming Priority (2)

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NZ50319900 2000-03-03
NZ503199 2000-03-03

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JP2001247459A JP2001247459A (ja) 2001-09-11
JP2001247459A5 true JP2001247459A5 (ja) 2006-12-07

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