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A Study of Pegcetacoplan in Pediatric Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
Sponsor: Apellis Pharmaceuticals, Inc.
Summary
The purpose of this study is to evaluate the safety, effectiveness, and biological activity (how the investigational medication is processed by the body) of pegcetacoplan in 12-17 year-olds (adolescents) who have paroxysmal nocturnal hemoglobinuria (PNH).
Official title: An Open Label, Single-Arm, Phase 2 Study to Evaluate the Safety, Pharmacokinetics, and Biologic Activity of Pegcetacoplan in Pediatric Patients With Paroxysmal Nocturnal Hemoglobinuria
Key Details
Gender
All
Age Range
12 Years - 17 Years
Study Type
INTERVENTIONAL
Enrollment
12
Start Date
2021-02-04
Completion Date
2028-12
Last Updated
2025-06-11
Healthy Volunteers
No
Interventions
Pegcetacoplan
Complement (C3) inhibitor
Locations (12)
Children's Hospital of Atlanta
Atlanta, Georgia, United States
Motol University Hospital
Prague, Czechia
Robert-Debré Hospital Paris
Paris, France
Hospital Ampang
Ampang, Malaysia
Radboud University Hospital Nijmegen
Nijmegen, Netherlands
University Medical Center Utrecht
Utrecht, Netherlands
University Children's Hospital
Belgrade, Serbia
University Hospital Vall d'Hebron
Barcelona, Spain
University Hospital 12 de Octubre
Madrid, Spain
Phramongkutklao Hospital and College of Medicine
Bangkok, Thailand
Maharaj Nakorn Chiang Mai hospital
Chiang Mai, Thailand
St. Mary's Hospital
London, United Kingdom