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ENROLLING BY INVITATION
NCT06435312
PHASE3

An Open-label Extension Study to Evaluate Subcutaneous Zilucoplan in Pediatric Participants With Generalized Myasthenia Gravis

Sponsor: UCB Biopharma SRL

View on ClinicalTrials.gov

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

Interventions

DRUG

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