A Phase 4 interventional study of Mirikizumab in Lactation and Inflammatory Bowel Disease, sponsored by Eli Lilly and Company. Recruiting at 20 sites in 7 countries. Open to female participants aged 3 Weeks and older. Per ClinicalTrials.gov, last updated 2026-09-08.
Sponsored by Eli Lilly and Company · Phase 4, Interventional, and Other
The main purpose of this study is to assess the amount of mirikizumab in breast milk in women who are breastfeeding who are receiving stable maintenance doses of mirikizumab for an approved indication.
Participation in this study could last up to 94 days, including screening and follow-up period.
262 studies on the registry are indexed under Breast Feeding; 112 are open to participants now.
This study's planned enrollment of 14 is below the median of 95 across 210 interventional studies indexed under Breast Feeding.
Browse Breast Feeding studies →Eli Lilly and Company is the lead sponsor of 2,048 studies on the registry; 140 are open to participants now.
Of its 521 completed or terminated interventional studies of FDA-regulated products, 341 (65%) have results posted.
Counted across the registry records on this site, refreshed daily.
Study Participants:
Note: in the opinion of the healthcare practitioner (HCP), there are no infant or maternal issues that would preclude the mother participant or the infant from participation
Exclusion Criteria:
Participants will continue to use previously prescribed Mirikizumab administered subcutaneously (SC).
Drug: Mirikizumab
Administered SC
Also known as: LY3074828
Concentration of Mirikizumab in Breast Milk
Time frame: Predose up to 28 Days
Pharmacokinetic (PK): Average Concentration During a Dosing Interval in Steady State of Mirikizumab in Breast Milk
Time frame: Predose up to 28 Days
Pharmacokinetic (PK): Area Under the Concentration Versus Time Curve Over a Dosing Interval [AUC(0-tau)] of Mirikizumab in Breast Milk
Time frame: Predose up to 28 Days
Breastfed Infant Safety as Assessed through Measurement of Infant Weight
Time frame: Predose up to 28 Days
Plan to share: Yes — Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.
Supporting information: Study protocol, Sap, Csr
No publications or documents are linked to this record.
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