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托莫西汀(LY139603)治疗新入院抑郁症患者的早期II期临床试验。

An early phase II clinical trial of tomoxetine (LY139603) in the treatment of newly admitted depressed patients.

作者信息

Chouinard G, Annable L, Bradwejn J

出版信息

Psychopharmacology (Berl). 1984;83(1):126-8. doi: 10.1007/BF00427436.

DOI:10.1007/BF00427436
PMID:6429697
Abstract

In a 6-week open-label study, ten newly admitted depressed patients were treated with tomoxetine , a selective inhibitor of noradrenaline reuptake. After 7 days of drug washout, patients were given an initial dose of 40 mg/day which was gradually increased to a maximum of 70 mg/day (median 50 mg/day). There was a statistically (P less than 0.001) and clinically significant improvement in the mean symptomatology of the patients measured on the Hamilton Depression Rating Scale. The drug had an early onset of action, a specific effect on mood, and no sedative properties.

摘要

在一项为期6周的开放标签研究中,10名新入院的抑郁症患者接受了托莫西汀治疗,托莫西汀是一种去甲肾上腺素再摄取选择性抑制剂。在停药7天后,患者开始服用初始剂量为40毫克/天的药物,该剂量逐渐增加至最大70毫克/天(中位数为50毫克/天)。根据汉密尔顿抑郁量表测量,患者的平均症状在统计学上(P小于0.001)和临床上均有显著改善。该药物起效早,对情绪有特定作用,且无镇静作用。

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本文引用的文献

1
A new inhibitor of norepinephrine uptake devoid of affinity for receptors in rat brain.一种对大鼠脑内受体无亲和力的去甲肾上腺素摄取新抑制剂。
J Pharmacol Exp Ther. 1982 Jul;222(1):61-5.
2
On the methods and theory of reliability.论可靠性的方法与理论。
J Nerv Ment Dis. 1976 Nov;163(5):307-17. doi: 10.1097/00005053-197611000-00003.
小鼠前额叶皮质对抗抑郁药的神经化学反应及其在焦虑样和抑郁样行为临床前模型中的疗效:一项比较和相关性研究。
Psychopharmacology (Berl). 2008 May;197(4):567-80. doi: 10.1007/s00213-008-1070-6. Epub 2008 Feb 15.
4
The search for new off-label indications for antidepressant, antianxiety, antipsychotic and anticonvulsant drugs.寻找抗抑郁药、抗焦虑药、抗精神病药和抗惊厥药的新的未标记适应症。
J Psychiatry Neurosci. 2006 May;31(3):168-76.
5
Clinical pharmacokinetics of atomoxetine.托莫西汀的临床药代动力学
Clin Pharmacokinet. 2005;44(6):571-90. doi: 10.2165/00003088-200544060-00002.
6
Non-stimulant medications in the treatment of ADHD.非兴奋剂药物治疗注意力缺陷多动障碍
Eur Child Adolesc Psychiatry. 2004;13 Suppl 1:I102-16. doi: 10.1007/s00787-004-1010-x.
7
Canine cataplexy is preferentially controlled by adrenergic mechanisms: evidence using monoamine selective uptake inhibitors and release enhancers.犬猝倒症优先受肾上腺素能机制控制:使用单胺选择性摄取抑制剂和释放增强剂的证据
Psychopharmacology (Berl). 1993;113(1):76-82. doi: 10.1007/BF02244337.