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 @ 7:07 PM
Ignite Modification Date:
2025-12-24 @ 7:07 PM
NCT ID:
NCT05892757
Eligibility Criteria:
Inclusion Criteria:
* Healthy, lactating, female volunteers who delivered one or more normal-term infants and established lactation from 1 - 6 months post-partum at the time of enrollment.
* Had a normal pregnancy (gestation of 37-42 weeks) with no clinically significant complications.
* Willing to permit the use of pasteurized donor milk, infant formula, or previously pumped/stored human milk to feed the infant.
* Agree to the use of provided breast pumps for the pumping of breast milk during the milk collection regimen of the study.
Exclusion Criteria:
\- Prior exposure to ubrogepant or atogepant within the past 30 days.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT05892757
Study Brief:
Protocol Section:
NCT05892757