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RecruitingNCT07612267Updated Sep 8, 2026

A Study to Measure Mirikizumab Levels in Breast Milk of Lactating Participants Receiving Mirikizumab Therapeutically for an Approved Indication

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

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Phase
Phase 4
Study type
Interventional
Enrollment
14
Allocation
Not applicable
Ages
3 Weeks and older
Sex
Female
01

Study summary

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.

02

Conditions studied

  • Lactation
  • Inflammatory Bowel Disease
03

In context

Breast Feeding

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
3 Weeks and older
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

Study Participants:

  • Mothers who are at minimum 18 years of age and their infants who are at least 36 weeks gestation age at birth and at least 3 weeks old by Study Day 0
  • Multiple births may be allowed following discussion with the medical monitor.

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

  • Lactation history is well established, with the mother exclusively breastfeeding her infant
  • Mother participant is receiving mirikizumab therapeutically for an approved diagnosis (having received at least 2 doses of mirikizumab SC maintenance therapy every 4 weeks prior to study Day 0)
  • Have a breastfed infant who can feed from a bottle with previously stored breast milk or formula

Exclusion criteria

Exclusion Criteria:

  • Have a history of inadequate lactation, for multiparous participants who have previously breastfed
  • Have a significant previous or current history of comorbidities capable of significantly altering the absorption, metabolism, or elimination of drugs, or of constituting a risk when taking mirikizumab, or of interfering with the interpretation of data
  • Have any condition that fulfills any contraindication stated in the label. All warnings and precautions stated in the label need to be considered
  • Have a history of breast augmentation procedures judged to have a clinical impact on breast milk expression such as breast reduction surgery and some breast implants, or current evidence of acute or chronic conditions affecting breasts and potentially interfering with breast milk collection
  • Have received any live vaccine (that is, live attenuated) within less than 4 weeks or inactivated vaccine within less than 2 weeks before enrollment or intend to receive a live vaccine during the study or an inactivated vaccine 2 weeks postdose, the mother participant must be given the vaccine at an injection site remote from mirikizumab administration
05

Study design

Phase
Phase 4
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
14 participants (estimated)

Study arms

  • Other
    Mirikizumab

    Participants will continue to use previously prescribed Mirikizumab administered subcutaneously (SC).

    Drug: Mirikizumab

Interventions

  • DrugMirikizumab

    Administered SC

    Also known as: LY3074828

06

What researchers measure

Primary outcomes

  1. Concentration of Mirikizumab in Breast Milk

    Time frame: Predose up to 28 Days

Secondary outcomes

  1. Pharmacokinetic (PK): Average Concentration During a Dosing Interval in Steady State of Mirikizumab in Breast Milk

    Time frame: Predose up to 28 Days

  2. 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

  3. Breastfed Infant Safety as Assessed through Measurement of Infant Weight

    Time frame: Predose up to 28 Days

07

Study locations

2 of 20 sites recruiting
  • Northwest Gastroenterologist
    Glenview, Illinois 60026-8000, United States
    • Nina Merel · Principal investigator
    Not yet recruiting
  • University of Iowa
    Iowa City, Iowa 52242, United States
    • Steven Polyak · Principal investigator
    Not yet recruiting
  • Johns Hopkins Bayview Medical Center
    Baltimore, Maryland 21224-2735, United States
    • Muniz Pedrogo David · Principal investigator
    Not yet recruiting
  • Digestive Disease Medicine of Central New York
    Utica, New York 13502, United States
    • Harvey Allen · Principal investigator
    Not yet recruiting
  • University Hospitals Cleveland Medical Center
    Cleveland, Ohio 44106, United States
    • Angelina Gangestad · Principal investigator
    Not yet recruiting
  • GI Research
    Columbia, V6G 2Z6, Canada
    • Yvette Leung · Principal investigator
    Not yet recruiting
  • Aarhus Universitetshospital, Aarhus Sygehus
    Aarhus N, 82000, Denmark
    • Mette Juelsgaard · Principal investigator
    Not yet recruiting
  • Slagelse Hospital
    Slagelse, 4200, Denmark
    • Natalia Pedersen · Principal investigator
    Not yet recruiting
  • Interdisziplinäres Crohn Colitis Centrum Rhein-Main
    Frankfurt am Main, 60594, Germany
    • Juergen Stein · Principal investigator
    Not yet recruiting
  • Klinikum Ernst von Bergmann
    Potsdam, D-14467, Germany
    • Daniel Baumgart · Principal investigator
    Not yet recruiting
  • Rabin Medical Center - PPDS
    HaMerkaz, Israel
    • Irit Avni-Biron · Principal investigator
    Not yet recruiting
  • Shaare Zedek Medical Center
    Jerusalem, 9013102, Israel
    • Ariella Shitrit · Principal investigator
    Recruiting
  • Chaim Sheba Medical Center
    Ramat Gan, 52621, Israel
    • Bella Ungar · Principal investigator
    Not yet recruiting
  • Tel Aviv Sourasky Medical Center Ichilov - PPDS
    Tel Aviv, 6423906, Israel
    • Nathaniel Cohen · Principal investigator
    Recruiting
  • Fondazione Policlinico Universitario A Gemelli - Rome - PPDS
    Lazio, 00136, Italy
    • Antonio Gasbarrini · Principal investigator
    Not yet recruiting
  • Ospedale San Raffaele S.r.l. - PPDS
    Lombardia, 20132, Italy
    • Silvio Danese · Principal investigator
    Not yet recruiting
  • Ospedale di Rho - UOC Gastroenterologia
    Rho, 20017, Italy
    • Simone Saibeni · Principal investigator
    Not yet recruiting
  • Ospedale Sandro Pertini
    Roma, 00157, Italy
    • Roberta Pica · Principal investigator
    Not yet recruiting
  • DC-MED Micha Kowalski S.K. - ul. Kilinskiego 6
    Radom, 26-610, Poland
    • Romanowski Janusz · Principal investigator
    Not yet recruiting
  • WIP Warsaw IBD Point Profesor Kierkus
    Warsaw, 04-501, Poland
    • Jaroslaw Kierkus · Principal investigator
    Not yet recruiting
08

References and documents

Individual participant data

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.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07612267
Lead sponsor
Eli Lilly and Company
Responsible party
Sponsor
First posted
May 28, 2026
Start date
Aug 5, 2026
Primary completion
Sep 2028 (estimated)
Completion
Sep 2028 (estimated)
Last update
Sep 8, 2026

Study contacts

Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
Contact
LillyTrials@Lilly.com
1-317-615-4559
Physicians interested in becoming principal investigators please contact
Contact
clinical_inquiry_hub@lilly.com
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST)
study director · Eli Lilly and Company

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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