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RECRUITING
NCT06055959
PHASE2/PHASE3

A 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 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

Interventions

DRUG

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