drugset / Trial / NCT03593200

A Phase IIa Study to Assess the Safety, Efficacy, and Pharmacokinetics of Subcutaneously Administered Pegcetacoplan (APL-2) in Subjects With PNH

NCT03593200

Phase 2 Completed 4 enrolled Apellis Pharmaceuticals, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase IIa, open-label, multiple dose, study in patients with PNH who have not received eculizumab (Soliris ®) in the past. A single cohort of subjects is planned for evaluation.

Timeline

Start
2018-08-16
Primary completion
2019-10-22
Completion
2019-10-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Pegcetacoplan Peptide 360 mg Subcutaneous