JP2005502690A5 - - Google Patents

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Publication number
JP2005502690A5
JP2005502690A5 JP2003526411A JP2003526411A JP2005502690A5 JP 2005502690 A5 JP2005502690 A5 JP 2005502690A5 JP 2003526411 A JP2003526411 A JP 2003526411A JP 2003526411 A JP2003526411 A JP 2003526411A JP 2005502690 A5 JP2005502690 A5 JP 2005502690A5
Authority
JP
Japan
Prior art keywords
day
chloroanilino
pyridylmethyl
pharmaceutical composition
phthalazine
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.)
Pending
Application number
JP2003526411A
Other languages
English (en)
Other versions
JP2005502690A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2002/010194 external-priority patent/WO2003022282A1/en
Publication of JP2005502690A publication Critical patent/JP2005502690A/ja
Publication of JP2005502690A5 publication Critical patent/JP2005502690A5/ja
Pending legal-status Critical Current

Links

Description

イバンドロン酸は、約1〜4mgの範囲で変化する用量で3〜4週間ごとにヒトに投与され得る。
パミドロン酸は、約15〜90mgの範囲で変化する用量で3〜4週間ごとにヒトに投与され得る。

Claims (7)

  1. (a)1−(4−クロロアニリノ)−4−(4−ピリジルメチルフタラジン、(b)オキサリプラチンおよび5−フルオロウラシル、ならびにフォリン酸を含み、ただしそれぞれの場合において有効成分は遊離形態または医薬上許容される塩形態で存在するものとし、さらに少なくとも1種の医薬上許容される担体を含んでいてもよい、同時、個別または連続使用される組合せ剤。
  2. 固形腫瘍疾患の処置に使用する、請求項1に記載の組合せ剤。
  3. 請求項1に記載の組合せ剤において、1−(4−クロロアニリノ)−4−(4−ピリジルメチル)フタラジンの血管形成に対して有効である量を含む、固形腫瘍疾患の処置のための医薬組成物。
  4. 組成物が500mg/日〜4000mg/日の範囲の用量の1−(4−クロロアニリノ)−4−(4−ピリジルメチル)フタラジン、またはその塩の均等内容量を含む、請求項3に記載の医薬組成物。
  5. 範囲が500mg/日〜2000mg/日である、請求項4に記載の医薬組成物。
  6. 組成物が500、1000、1500または2000mg/日の1−(4−クロロアニリノ)−4−(4−ピリジルメチル)フタラジン、またはその塩の均等内容量を含む、請求項5に記載の医薬組成物。
  7. 腫瘍疾患が結腸直腸癌である、請求項3〜6のいずれか1項に記載の医薬組成物。
JP2003526411A 2001-09-12 2002-09-11 癌治療についての4−ピリジルメチルフタラジンの使用 Pending JP2005502690A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US31869401P 2001-09-12 2001-09-12
US33102501P 2001-09-12 2001-09-12
US32204401P 2001-09-14 2001-09-14
US38816302P 2002-06-12 2002-06-12
PCT/EP2002/010194 WO2003022282A1 (en) 2001-09-12 2002-09-11 Use of 4-pyridylmethylphthalazines for cancer treatment

Publications (2)

Publication Number Publication Date
JP2005502690A JP2005502690A (ja) 2005-01-27
JP2005502690A5 true JP2005502690A5 (ja) 2009-08-06

Family

ID=27502161

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003526411A Pending JP2005502690A (ja) 2001-09-12 2002-09-11 癌治療についての4−ピリジルメチルフタラジンの使用

Country Status (22)

Country Link
US (2) US20040258770A1 (ja)
EP (1) EP1427420B1 (ja)
JP (1) JP2005502690A (ja)
KR (1) KR20040029172A (ja)
CN (1) CN1330308C (ja)
AT (2) ATE421880T1 (ja)
AU (2) AU2002342678B2 (ja)
BR (1) BR0212446A (ja)
CA (1) CA2457848A1 (ja)
CO (1) CO5560545A2 (ja)
CY (1) CY1105189T1 (ja)
DE (2) DE60231068D1 (ja)
DK (1) DK1427420T3 (ja)
ES (2) ES2266590T3 (ja)
HR (1) HRP20040241A2 (ja)
IL (1) IL160382A0 (ja)
NO (1) NO327358B1 (ja)
NZ (1) NZ531484A (ja)
PL (1) PL367349A1 (ja)
PT (1) PT1427420E (ja)
RS (1) RS16804A (ja)
WO (1) WO2003022282A1 (ja)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0223341D0 (en) * 2002-10-08 2002-11-13 Groningen Acad Ziekenhuis Organic compounds
WO2004058234A2 (en) * 2002-12-27 2004-07-15 Schering Aktiengesellschaft Pharmaceutical combinations of phthalazine vegf inhibitors and benzamide hdac inhibitors
WO2004105747A1 (en) * 2003-05-20 2004-12-09 Aronex Pharmaceuticals, Inc Combination chemotherapy comprising capecitabine and a liposomal platinum complex
US20080085902A1 (en) * 2003-09-23 2008-04-10 Guido Bold Combination Of A Vegf Receptor Inhibitor Or With A Chemotherapeutic Agent
GB0610925D0 (en) * 2006-06-02 2006-07-12 Novartis Ag Use of vascular endothelial growth factor receptor inhibitors for the treatment of cancer
KR101037292B1 (ko) * 2010-09-03 2011-05-27 (주)슈추어 신발 장식구

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2224130T3 (es) * 1994-08-09 2005-03-01 Eisai Co., Ltd. Compuesto de piridazina condensada.
KR100489174B1 (ko) * 1996-03-05 2005-09-30 제네카-파마 소시에떼아노님 4-아닐리노퀴나졸린유도체
US6096904A (en) * 1996-12-03 2000-08-01 The Trustees Of The University Of Pennsylvania Synthetic techniques and intermediates for polyhydroxy, dienyl lactone derivatives
CO4950519A1 (es) * 1997-02-13 2000-09-01 Novartis Ag Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion

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