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临床试验/IRCT20220209053979N10
IRCT20220209053979N10尚未招募Unknown

Bioequivalence Study of Carvedilol 12.5 mg tablet manufactured by Shafa Pharmaceutical and Coreg manufactured by GSK in 24 Healthy Volunteers under fed condition

Shafa 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
Unknown
状态
尚未招募
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 55 years(—)
性别
All

入选标准

  • Healthy male or female volunteers
  • Body mass index (BMI) between 18 - 30
  • Volunteers who are willing to sign an informed consent form

排除标准

  • Familial history of heart disease
  • History of allergy to Carvedilol or formulation components
  • History or significant clinical evidence of any disease
  • Taking any type of medicine in the 14 days before the start of the study
  • Participation in any clinical study within 30 days prior to study initiation
  • Systolic blood pressure less than 11 and diastolic less than 7 mmHg

研究者

发起方
Shafa Pharmaceutical Company

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