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:
2025-12-25 @ 4:57 AM
Ignite Modification Date:
2025-12-25 @ 4:57 AM
NCT ID:
NCT04742218
Eligibility Criteria:
Inclusion Criteria:
* Subject provides written informed consent before any study-specific evaluation is performed;
* Subject is a healthy adult male or female volunteer between the ages of 18 and 45 years, inclusive, at screening;
* Subject has a BMI of 18 to 30 kg/m2, inclusive, at screening
* Subject meets all inclusion criteria outlined in the clinical study protocol
Exclusion Criteria:
* Subject is a woman who is pregnant or breastfeeding;
* Subject has clinically significant abnormalities in the screening or check-in assessments;
* Subject has received an investigational drug within 30 days or 5 half-lives (whichever is longer) before the first dose of study drug
* Subject does not meet any other exclusion criteria outlined in clinical study protocol.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT04742218
Study Brief:
Protocol Section:
NCT04742218