Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:31 PM
Ignite Modification Date:
2025-12-24 @ 6:31 PM
NCT ID:
NCT02114957
Eligibility Criteria:
Inclusion Criteria:
* Health subjects weighing between 50 to 91 kilograms (110 to 200 pounds)
* Subjects 18 to 65 years of age
* Subjects having normal hepatic, renal and bone marrow function as assessed by history, physical and clinical chemistry analysis
Exclusion Criteria:
* Subjects positive for HIV, HBV and HCV
* Subjects with diabetes-due to length of fasting
* Subjects regularly taking any kind of prescription medications
* Subjects taking oral contraception, hormone-containing IUDs, contraception implants, or Depo medroxyprogesterone injections
* Subjects taking any food or herbal supplements containing AGN (e.g. CognIQTM, D-Cursinol, Decursinol-50™, Ache Action™, Fast-Acting Joint Formula, EstroG-100™) within 30 days of the study.
* Female subjects that are pregnant, \<6 months postpartum, or breastfeeding women.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT02114957
Study Brief:
Protocol Section:
NCT02114957