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Drug Evaluations

The development of the tumor vascular-disrupting agent ASA404 (vadimezan, DMXAA): current status and future opportunities

, MB ChB & , FRACP FRCP(Edin) PhD
Pages 295-304 | Published online: 06 Jan 2010

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Wenkui Li, Hui Lin, Harold T. Smith & Francis L.S. Tse. (2011) Developing a robust ultrafiltration-LC–MS/MS method for quantitative analysis of unbound vadimezan (ASA404) in human plasma. Journal of Chromatography B 879:21, pages 1927-1933.
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Xuexin He, Su Li, He Huang, Zhiming Li, Likun Chen, Sheng Ye, Jiajia Huang, Jing Zhan & Tongyu Lin. (2011) A pharmacokinetic and safety study of single dose intravenous combretastatin A4 phosphate in Chinese patients with refractory solid tumours. British Journal of Clinical Pharmacology 71:6, pages 860-870.
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A Palumbo, F Hauler, P Dziunycz, K Schwager, A Soltermann, F Pretto, C Alonso, G F Hofbauer, R W Boyle & D Neri. (2011) A chemically modified antibody mediates complete eradication of tumours by selective disruption of tumour blood vessels. British Journal of Cancer 104:7, pages 1106-1115.
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Kari Ann Shirey, Quan M Nhu, Kevin C Yim, Zachary J Roberts, John R Teijaro, Donna L Farber, Jorge C Blanco & Stefanie N Vogel. (2011) The anti-tumor agent, 5,6-dimethylxanthenone-4-acetic acid (DMXAA), induces IFN-β-mediated antiviral activity in vitro and in vivo. Journal of Leukocyte Biology 89:3, pages 351-357.
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Shi-Jie Zhang & Wei-Xiao Hu. (2010) Vadimezan: 2-(5,6-dimethyl-9-oxo-9 H -xanthen-4-yl)acetic acid . Acta Crystallographica Section E Structure Reports Online 66:8, pages o2082-o2083.
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