A randomized, single-dose, double-blind, multi-sequence crossover, study to assess the bioavailability of free curcumin in various curcumin formulations in comparison with standard curcumin in health volunteers.

incy Benzy Joshua0 个研究点目标入组 80 人开始时间: 待定最近更新: 2023年12月19日

试验速览

暂无简介。

•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 who have consumed curcumin containing food 2 days prior to screening
•2.Subjects having symptoms of viral infections
•3.Pregnant or lactating women.
•4.Subjects with known hypersensitivity to the investigational products.
•5.Subjects who have participated in any clinical trial in the past 1 month.
•6.Any subjects found to have entered in to the study in violation of this protocol or if the subject is uncooperative during the study.
•7.Any other condition that in the opinion of the investigator that does not justify the subject’s participation in the trial.

发起方

incy Benzy Joshua