drugset / Trial / NCT02588833

Pilot Study to Assess Safety, Preliminary Efficacy and Pharmacokinetics of S.C. Pegcetacoplan (APL-2) in PNH Subjects.

NCT02588833

Phase 1 Completed 23 enrolled Apellis Pharmaceuticals, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The objectives of the study are to assess the safety, tolerability, preliminary efficacy and PK of multiple subcutaneous (SC) doses of pegcetacoplan in subjects with paroxysmal nocturnal hemoglobinuria (PNH) who have not received treatment with eculizumab in the past. An exploratory objective of the study is to assess the pharmacodynamics (PD) of multiple SC doses of pegcetacoplan when administered to PNH patients.

Timeline

Start
2015-12-01
Primary completion
2019-08-26
Completion
2019-08-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Pegcetacoplan Peptide 180 mg Subcutaneous
Subject Pegcetacoplan Peptide 270 mg Subcutaneous