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A Study to Evaluate Subcutaneous Zilucoplan in Pediatric Participants With Generalized Myasthenia Gravis
Sponsor: UCB Biopharma SRL
Summary
The purpose of this study is to assess the pharmacokinetics, pharmacodynamics, safety, tolerability, immunogenicity and activity of zilucoplan (ZLP) in pediatric study participants with generalized myasthenia gravis (gMG).
Official title: A Multicenter Open-Label, Uncontrolled Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, Tolerability, and Activity of Zilucoplan in Pediatric Study Participants From 2 to Less Than 18 Years of Age With Acetylcholine Receptor Antibody Positive Generalized Myasthenia Gravis
Key Details
Gender
All
Age Range
12 Years - 17 Years
Study Type
INTERVENTIONAL
Enrollment
8
Start Date
2024-10-16
Completion Date
2026-12-25
Last Updated
2026-03-27
Healthy Volunteers
No
Conditions
Interventions
Zilucoplan
Zilucoplan will be administered subcutaneously to pediatric study participants.
Locations (9)
Mg0014 50168
Chicago, Illinois, United States
Mg0014 50574
Flower Mound, Texas, United States
Mg0014 40144
Milan, Italy
Mg0014 40774
Katowice, Poland
Mg0014 40218
Warsaw, Poland
Mg0014 20104
Seoul, South Korea
Mg0014 20220
Seoul, South Korea
Mg0014 40735
Glasgow, United Kingdom
Mg0014 40736
London, United Kingdom