Overview

A Safety Extension Study in Patients With Erythropoietic Protoporphyria (EPP)

Status:
Completed
Trial end date:
2014-02-27
Target enrollment:
Participant gender:
Summary
The main objectives of the study were to evaluate the safety and tolerability of afamelanotide by measuring treatment emergent adverse events (AEs) and to determine whether afamelanotide can improve the quality of life of EPP patients.
Phase:
Phase 3
Details
Lead Sponsor:
Clinuvel Pharmaceuticals Limited
Treatments:
Afamelanotide