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巴泽多昔芬(惠氏公司)。

Bazedoxifene (Wyeth).

作者信息

Gruber Christian, Gruber Doris

机构信息

Department of Gynecological Endocrinology and Reproductive Medicine, University of Vienna Medical School, A-1090 Vienna, Wahringer Gurtel 18-20, Austria.

出版信息

Curr Opin Investig Drugs. 2004 Oct;5(10):1086-93.

PMID:15535430
Abstract

Bazedoxifene is a tissue-specific selective estrogen receptor modulator being developed by Wyeth Pharmaceuticals (formerly Wyeth-Ayerst Laboratories) to be used alone for the prevention and treatment of osteoporosis in postmenopausal women and in combination with Premarin for menopausal symptoms. As of March and June 2004, worldwide phase III trials for bazedoxifene, and bazedoxifene in combination with Premarin, were ongoing.

摘要

巴泽多昔芬是惠氏制药公司(前身为惠氏-艾尔斯特实验室)正在研发的一种组织特异性选择性雌激素受体调节剂,拟单独用于预防和治疗绝经后女性的骨质疏松症,并与结合雌激素联合用于治疗更年期症状。截至2004年3月和6月,巴泽多昔芬以及巴泽多昔芬与结合雌激素联合用药的全球III期试验正在进行中。

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Bazedoxifene (Wyeth).巴泽多昔芬(惠氏公司)。
Curr Opin Investig Drugs. 2004 Oct;5(10):1086-93.
2
Efficacy and safety of bazedoxifene, a novel selective estrogen receptor modulator for the prevention and treatment of postmenopausal osteoporosis.用于预防和治疗绝经后骨质疏松症的新型选择性雌激素受体调节剂——巴多昔芬的疗效和安全性。
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Bazedoxifene: a new selective estrogen receptor modulator for the treatment of postmenopausal osteoporosis.巴多昔芬:一种用于治疗绝经后骨质疏松症的新型选择性雌激素受体调节剂。
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Bazedoxifene: a third-generation selective estrogen receptor modulator for treatment of postmenopausal osteoporosis.巴多昔芬:一种用于治疗绝经后骨质疏松症的第三代选择性雌激素受体调节剂。
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Bazedoxifene: bazedoxifene acetate, TSE 424, TSE-424, WAY 140424.巴多昔芬:醋酸巴多昔芬、TSE 424、TSE - 424、WAY 140424。
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Bazedoxifene: a new selective estrogen receptor modulator for postmenopausal osteoporosis.巴多昔芬:一种用于绝经后骨质疏松症的新型选择性雌激素受体调节剂。
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[Bazedoxifene as a new-generation SERM].[巴多昔芬作为新一代选择性雌激素受体调节剂]
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Tissue-selective estrogen complexes with bazedoxifene prevent metabolic dysfunction in female mice.贝达昔芬与雌二醇形成的组织选择性雌激素复合物可预防雌性小鼠代谢功能障碍。
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Efficacy and safety of bazedoxifene for postmenopausal osteoporosis.巴泽多昔芬治疗绝经后骨质疏松症的疗效和安全性。
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