drugset / Trial / NCT04558918

Study of Efficacy and Safety of Twice Daily Oral LNP023 in Adult PNH Patients With Residual Anemia Despite Anti-C5 Antibody Treatment

NCT04558918 ↗

Phase 3 Completed 97 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

This study was a multi-center, randomized, open-label, active comparator-controlled, parallel group study. The purpose of this Phase 3 study in PNH patients presenting with residual anemia despite treatment with anti-C5 antibody, was to determine whether iptacopan is efficacious and safe for the treatment of PNH through demonstration of superiority of iptacopan compared to anti-C5 antibody treatment.

Timeline

Start
2021-01-25
Primary completion
2022-09-26
Completion
2023-03-06

Outcome

Met primary endpoint

registry analysis (superiority test); LNP023 200mg b.i.d. vs Anti-C5 Antibody; p <0.0001 NCT04558918 ↗

release “pivotal Phase III APPLY-PNH trial met its two primary endpoints” novartis.com ↗

release “APPLY-PNH trial in patients with residual anemia (hemoglobin < 10 g/dL) despite prior anti-C5 treatment who switched to Fabhalta, which demonstrated superiority” novartis.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Eculizumab Monoclonal antibody — Intravenous
Subject Iptacopan Small molecule 200 mg Oral
Comparator Ravulizumab Monoclonal antibody — Intravenous