Survey to Identify Burdens and Unmet Needs of Patients With Epidermolysis Bullosa

Launched by AMICUS THERAPEUTICS · May 16, 2017

Keywords

ClinConnect Summary

Epidermolysis bullosa (EB) is a rare, often severe genetic disorder characterized by mechanical fragility and blistering or erosion of the skin, mucosa, or epithelial lining of other organs, in response to little or no apparent trauma.

EB is chronic, potentially disfiguring, and in some cases fatal. Patients with EB have painful wounds and blisters that can lead to infection and scarring. There are many genetic and symptomatic variations of EB, but all forms share the common symptom of fragile skin that blisters and tears, sometimes from the slightest friction or trauma. There is currently...

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Confirmed diagnosis of EB including subtype
• • Resident of the US
• • Informed Consent
• • Patient must be 18 years or older
• • If the survey is done by a caregiver, they must be a parent or legal guardian and must be 18 years or older to answer on behalf of a patient under 18 years or on behalf of a patient 18 years or older who is unable to answer for themselves.
• • Must participate in and complete a one hour telephone interview
• Exclusion Criteria:
• • Patient failing to meet the inclusion criteria above