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RECRUITING
NCT04901936
PHASE2

A Study of Pegcetacoplan in Pediatric Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

Sponsor: Apellis Pharmaceuticals, Inc.

View on ClinicalTrials.gov

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

DRUG

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