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An Open-label Extension 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 long-term safety and tolerability of an additional 52 weeks of Zilucoplan treatment administered by subcutaneous injection once daily in pediatric study participants
Official title: An Open-Label Extension Study to Evaluate the Long-Term Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Activity of Zilucoplan in Pediatric Study Participants With Acetylcholine Receptor Antibody Positive Generalized Myasthenia Gravis
Key Details
Gender
All
Age Range
12 Years - Any
Study Type
INTERVENTIONAL
Enrollment
8
Start Date
2024-11-19
Completion Date
2027-11-19
Last Updated
2026-03-27
Healthy Volunteers
No
Conditions
Interventions
Zilucoplan
Zilucoplan will be administered subcutaneously to pediatric study participants
Locations (7)
Mg0015 40144
Milan, Italy
Mg0015 40774
Katowice, Poland
Mg0015 40218
Warsaw, Poland
Mg0015 20104
Seoul, South Korea
Mg0015 20220
Seoul, South Korea
Mg0015 40735
Glasgow, United Kingdom
Mg0015 40736
London, United Kingdom