Epidermolysis Bullosa Simplex
Epidermolysis bullosa simplex (EBS) is a rare genetic skin disorder characterized by extremely fragile skin that blisters easily, often in response to minor injuries or friction.
We are investigating whether apremilast can improve symptoms in patients over 6 years old with epidermolysis bullosa simplex. The study will also look at the safety of the treatment and how it affects quality of life.
Health conditions and diseases that the clinical trial is designed to study and treat.
Epidermolysis bullosa simplex (EBS) is a rare genetic skin disorder characterized by extremely fragile skin that blisters easily, often in response to minor injuries or friction.
These questions help us understand your situation so we can let the trial team know whether you might be a potential match. This is not a medical evaluation and is not part of the official screening, the study doctor will make the final decision..
Don't worry if you don't know the medicines tested in the trial. There is a chance you have heard about the similar medicines. Check the list below to see if you are familiar with any of them.
Locations and medical facilities where this clinical trial is currently recruiting or conducting research. Select the locations where you would like to participate.
Disclaimer: Parts of this content have been automatically extracted from the EU Clinical Trials registry. While we strive for accuracy, please always contact the trial site or sponsor directly for correct and official information before making any decisions about participation. View on EU Clinical Trials.