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

Outcome

Met primary endpoint

registry analysis (superiority test); Pegcetacoplan to Pegcetacoplan vs Eculizumab to Pegcetacoplan; p <0.0001; LS mean difference 3.84 (95% CI 2.33 to 5.34); NCT03500549 ↗

paper Pegcetacoplan was superior to eculizumab with respect to the change in hemoglobin level from baseline to week 16, with an adjusted (least squares) mean difference of 3.84 g per deciliter (P<0.001). PMID 33730455 ↗

Publications

Drugs

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