Gefurulimab
Combination ProductCombination product consisting of syringe prefilled with gefurulimab will be administered weekly via subcutaneous (SC) injection.
NCT Number: NCT06607627
The primary objective of this study is to assess the pharmacokinetics and pharmacodynamics of gefurulimab in pediatric participants with AChR+ gMG for the duration of the study.
Interested in participating?
Request Info6 year–17 year
All sexes
Interventional
Phase 3
Research Site, Joinville, Brazil
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
United States of America (USA) specific inclusion criterion:
Rest of World (ROW) specific inclusion criteria:
Global inclusion criteria:
Exclusion criteria
Combination product consisting of syringe prefilled with gefurulimab will be administered weekly via subcutaneous (SC) injection.
Time frame: Day 1 predose through Week 18 predose
Time frame: Day 1 predose through Week 18 predose
Time frame: Day 1 through Week 134
Time frame: Baseline through Week 18
Time frame: Baseline through Week 18
Time frame: Baseline through Week 18
Time frame: Baseline through Week 18
Time frame: Baseline through Week 134
Time frame: Baseline through Week 134
Time frame: Baseline through Week 134
Contact information is provided by the study sponsor or research team.
Alexion Pharmaceuticals, Inc.
Industry
An Open-Label, Single-arm Study to Evaluate the Pharmacokinetics (PK), Pharmacodynamics (PD), Safety, and Efficacy of Gefurulimab in Pediatric Patients (6 to < 18 Years of Age) With Generalized Myasthenia Gravis (gMG) Who Express Acetylcholine Receptor Antibodies (AChR+)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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