跳至主要内容
临床试验/CTRI/2019/03/017991
CTRI/2019/03/017991尚未招募1 期

To Evaluate the Safety, Tolerability and Sensory Evaluation of HQMZ111831 in Healthy Female Volunteers: Randomized Open Label, Two Arm Clinical Study - Quista_M

The Himalaya Drug Company0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
尚未招募

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

入选标准

  • 1)Healthy Adult female volunteers.
  • 2)Aged >=18 to <= 45 years.
  • 3)Subjects willing to sign the informed consent.
  • 4)Subjects to be refrained to take any other similar kind of intervention during the study period.

排除标准

  • 1)Subjects clinically diagnosed with any clinically significant systemic disorder.
  • 2)Subjects on any other nutritional supplements.
  • 3)A known history or present condition of allergic response to pharmaceutical products its components or ingredients in the test products.
  • 4)Genetic and Endocrinal disorders.
  • 5)Has participated in a similar clinical investigation in the past four weeks.
  • 6)Subjectâ??s parents who refused to sign informed consent.

研究者

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