A comparative Bioavailability study of CCL in Healthy Volunteers
- Registration Number
- CTRI/2020/07/026856
- Lead Sponsor
- Akay Natural Ingredients Pvt Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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 food containing any ingredients of the formulation within 2 days prior to screening
2. Subjects having symptoms of viral infection, including COVID-19 infection
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 subjectâ??s participation in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method