Endoxifen, a New Cornerstone of Breast Cancer Therapy: Demonstration of Safety,Tolerability, and Systemic Bioavailability in Healthy Human Subjects

被引:59
作者
Ahmad, A. [1 ]
Shahabuddin, S. [1 ]
Sheikh, S. [1 ]
Kale, P. [2 ]
Krishnappa, M. [2 ]
Rane, R. C. [3 ]
Ahmad, I. [1 ]
机构
[1] Jina Pharmaceut Inc, Libertyville, IL USA
[2] Lambda Therapeut Res Ltd, Ahmadabad, Gujarat, India
[3] Intas Pharmaceut Ltd, Ahmadabad, Gujarat, India
关键词
RECEIVING ADJUVANT TAMOXIFEN; CLINICAL-OUTCOMES; CYP2D6; METABOLISM; CYP2D6-ASTERISK-10; PHARMACOGENETICS; PREVENTION; GENOTYPES; SURVIVAL; IMPACT;
D O I
10.1038/clpt.2010.196
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Endoxifen is an active metabolite of tamoxifen, a drug used in the treatment of breast cancer. In order to be clinically effective, tamoxifen must be converted to endoxifen by cytochrome P450 2D6 (CYP2D6). A study involving single escalating oral doses was conducted in humans to evaluate the safety, tolerability, and pharmacokinetics (PK) of endoxifen. This is the first study demonstrating that single oral doses of endoxifen are safe and well tolerated and have sufficient bioavailability to reach systemically effective levels in human subjects. Furthermore, it was found that endoxifen is rapidly absorbed and systemically available and that it displays dose proportionality in peak drug concentrations in plasma (C-max) and area under the concentration-time curve extrapolated from 0 to infinity (AUC(0-infinity).) over the dose range 0.5-4.0 mg.
引用
收藏
页码:814 / 817
页数:4
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