Clinical Trials Directory

Trials / Completed

CompletedNCT02537054

Intravitreal Aflibercept for Therapy of Patients With Pseudoxanthoma Elasticum (PXE)

Intravitreal Aflibercept (Eylea) for Therapy of Choroidal Neovascularization (CNV) and Fibrovascular Proliferation (FVP) in Patients With Pseudoxanthoma Elasticum (PXE)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
15 (actual)
Sponsor
University Hospital, Bonn · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether Aflibercept (Eylea) is effective in the treatment of choroidal neovascularization and fibrovascular proliferation in patients with pseudoxanthoma elasticum (PXE) in terms of preservation or improvement of visual acuity.

Conditions

Interventions

TypeNameDescription
DRUGAfliberceptIntravitreal injection

Timeline

Start date
2015-09-01
Primary completion
2018-07-02
Completion
2018-07-02
First posted
2015-09-01
Last updated
2019-05-07

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02537054. Inclusion in this directory is not an endorsement.