Clinical Trial

Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of ALXN2230 in Healthy Participants

Recruiting Phase 1
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Summary
The primary objective of this study is to evaluate the safety and tolerability of single subcutaneous (SC) doses of ALXN2230 in healthy participants.
Protocol Amendment History 1 change
critical Recruitment opened 2026-04-10
Trial Details
NCT Number NCT07352423
Lead Sponsor Alexion Pharmaceuticals, Inc.
Conditions Healthy Adult Participants
Enrollment 48 participants
Start Date 2026-03-26
Primary Completion 2026-12-23 (estimated)
Study Completion 2026-12-23 (estimated)
Updated on ClinicalTrials.gov 2026-04-09