drugset / Trial / NCT03500549

Study to Evaluate the Efficacy and Safety of APL-2 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

NCT03500549

Phase 3 Completed 80 enrolled Apellis Pharmaceuticals, Inc.
RandomizedCrossoverOpen-labelTreatment

Summary

Evaluation of the Efficacy and Safety of APL-2 in Patients with Paroxysmal Nocturnal Hemoglobinuria

Timeline

Start
2018-06-14
Primary completion
2019-11-14
Completion
2020-08-13

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Eculizumab Monoclonal antibody Intravenous
Subject Pegcetacoplan Peptide 1080 mg Subcutaneous