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A Study to Assess Zilucoplan Concentration in Breast Milk of Healthy Lactating Women

StatusRecruiting
PhasePhase 1
Started2025-07-09
View on ClinicalTrials.gov ↗

Amendment history

2026-08-26
Study Status, Contacts/Locations v6
Study sitesdetails revised at 1 of 2 sites
2026-03-19
Study Status v5
Primary completion date2026-07-22→2027-03-23
Completion date2026-07-22→2027-03-23
2025-08-04
Study Status v4
Primary completion date2026-05-25→2026-07-22
Completion date2026-05-25→2026-07-22
2025-07-30
2 amendments v2-v3
2 re-verifications since 2025-07-21, no change to tracked fields
2025-07-16
Not Yet Recruiting→Recruiting Study Status, Study Description, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2025-05-12→confirmed 2025-07-09
Study sites0→2
2025-04-29
Original filing
The purpose of this study is to assess the steady state (SS) concentrations of zilucoplan (ZLP) and its major metabolites in mature breast milk of healthy study participants following injection of repeated once-daily doses of ZLP.
Trial Details
NCT Number NCT06961747
Lead Sponsor UCB Biopharma SRL
Conditions Healthy Participants
Enrollment 15 participants
Start Date 2025-07-09
Primary Completion 2027-03-23 (estimated)
Study Completion 2027-03-23 (estimated)
Updated on ClinicalTrials.gov 2026-08-27