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

Erythropoietic Protoporphyria Clinical Trial

Official title:
A Phase III, Safety Extension Study in Patients With Erythropoietic Protoporphyria (EPP)

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04578496
Study type Interventional
Source Clinuvel Pharmaceuticals Limited
Contact
Status Completed
Phase Phase 3
Start date July 11, 2011
Completion date February 27, 2014
View Details
See also
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