IRCT20200105046010N21招募中未知
Pharmacokinetic assessments of Neotadin® tablet with brand drugs AERIUS® 5mg, FC Schering-Plough Belgium.
ABIDI Pharmaceutical Company0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 24
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 60 years(—)
- 性别
- All
入选标准
- •General health
- •Body mass index(18-28)
- •Informed consent
- •Age(18-60)
排除标准
- •A history of cardiovascular disease
- •A history of liver & kidney disease
- •Alcohol & Drug addiction
- •Hypersensitivity to the drug
研究者
相似试验
进行中(未招募)
不适用
Evaluation of pharmacokinetic and pharmacodynamic interactions between escitalopram and drugs used for the treatment of bipolar disorders. - NDbipolar disordersMedDRA version: 9.1Level: LLTClassification code 10057667Term: Bipolar disorderEUCTR2008-000370-20-ITAZIENDA OSPEDALIERA PISANA
尚未招募
不适用
In-vivo Bioequivalence Test of Tramadol® tablet with brand drugs (ULTRAM® 100mg, Junssen Cilage, Switzerland).In this study, the disease is not examined. Subject bioequivalence test and reference tablets Tramadol studied..IRCT20200105046010N23Zagross Darou Pharmaceutical Company24
进行中(未招募)
不适用
Farmacokinetische evaluatie van enteraal toegediende omeprazole-suspensie bij patiënten met cerebral palsy.gastro-oesophagale refluxMedDRA version: 9.1Level: LLTClassification code 10017924Term: Gastroesophageal refluxEUCTR2007-000099-17-BEniversity Hospital Gent
已完成
不适用
Supralimus-Core(TM) Pharmacokinetic(PK) StudyCTRI/2009/091/000426Sahajanand Medical Technologies Pvt Ltd20
尚未招募
不适用
In-vivo Bioequivalence Test Fampridine tablet with brand drug FAMPYRA Made by Biogen Idec, UK.The aim of this study is evaluation of bioequivalence of test and reference drugs and the study will one by healthy volunteers.IRCT20200105046010N19Pharan shimi Pharmaceutical Company24
