CTRI/2022/06/043510尚未招募未知
An Open-Label, Single-Arm Clinical Study to evaluate the Safety and Tolerability of Purim Tablet in Healthy Adultsâ??
试验速览
- 阶段
- 未知
- 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 subjects of either sex aged between >=18 to <=50 years.
- •2. Subjects willing to sign informed consent and follow the study procedure.
- •3. Has not participated in a similar investigation in the past four weeks.
- •4. Subjects willing to refrain taking any other nutritional supplement during the study period
排除标准
- •1. Subjects with clinically significant serious cardiovascular, cerebrovascular, respiratory, liver, renal disease, congenital or any other disorder.
- •2. Subjects with any abnormal lab values detected at screening shall be excluded.
- •3. A known history or present condition of allergic response to pharmaceutical products its components or ingredients in the investigational products (IP).
- •4. Pre-existing systemic disease necessitating long-term medications.
- •5. Genetic and endocrinal disorders.
- •6. Subjects who refused to sign informed consent.
- •7. Pregnant and lactating women.
研究者
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