A randomized, single-dose, double-blind, 2-way crossover,2-sequence study to assess the bioavailability of FF-20 incomparison with normal unformulated active ingredient (UF)supplementation in healthy volunteers.

Akay Natural Ingredients Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新: 2021年11月24日

研究概览

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•1.Subjects who are willing to give their written informed consent and comply with the protocol
•requirements.
•2. Females of child bearing age, agree to use approved birth control methods during the study, and have
•negative urine pregnancy test (UPT) at screening
•3. Subject understands the study procedures, is ready to comply and provide signed informed consent
•form (ICF) to participate in the study

•1.Subjects having symptoms of viral infection, including COVID-19 infection
•2. Pregnant or lactating women.
•3. Subjects with known hypersensitivity to the investigational products.
•4. Subjects who have participated in any clinical trial in the past 1 month.
•5. Any subjects found to have entered in to the study in violation of this protocol or if the subject is
•uncooperative during the study.
•6. Any other condition that in the opinion of the investigator that does not justify the subjectâ??s
•participation in the trial.

发起方

Akay Natural Ingredients Pvt Ltd