Epidermolysis Bullosa

3

Review clinical trials related to Epidermolysis Bullosa. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Targeting Collagen VII Antibodies With IV IgG in Dystrophic Epidermolysis Bullosa

The study objective is to see if IV IgG treatment in Recessive Dystrophic Epidermolysis Bullosa (RDEB) skin in conjunction with VYJUVEK treatment improves wound healing and affects the levels of C7 and HSV-1 antibody levels in serum. Fewer wounds, more rapidly healing wounds, and decreased C7 and HSV-1 antibodies could improve quality of life.

Participants needed: 8
Trial details
Phase: Phase 1, Phase 2Age: 6+Biological sex: AllType: InterventionalSponsor: M. Peter MarinkovichUpdated: May 5, 2026Locations: 1
Eligibility criteria

Diagnosis of generalized Recessive dystrophic epidermolysis bullosa (RDEB) demon... [+5]

History of thrombotic event(s) [+3]

Status: Recruiting

A Study to Learn About the Safety and Efficacy of the Drug Oleogel-S10 in Japanese Patients With Epidermolysis Bullosa

The goal of this clinical trial is to learn if Oleogel-S10 gel works to treat skin wounds from two types of inherited epidermolysis bullosa (EB): junctional EB (JEB) or dystrophic EB (DEB) in the Japanese population. Children and adults may participate. The trial also looks at the safety of Oleogel-S10 gel. The main questions it will answer are: * Does Oleogel-S10 gel close wounds from JEB or DEB within 45 days or reduce the size of the wounds? * Are there any medical problems when using Oleogel-S10 gel? * How much of the drug ends up in your blood? The study has 2 parts. In Part 1, participants will: * Apply Oleogel-S10 gel to the EB wound dressings at least once every 4 days for 45 days. * Visit the clinic once every 2 weeks for checkups and tests. If participants complete Part 1, they may participate in Part 2 if they choose to. In Part 2, participants will continue to receive Oleogel-S10 gel until the product is available to buy in Japan or until the trial is stopped by the company.

Participants needed: 6
Trial details
Phase: Phase 3Age: 21+Biological sex: AllType: InterventionalSponsor: Chiesi Farmaceutici S.p.A.Updated: Dec 22, 2025Locations: 6
Eligibility criteria

Male or female aged ≥ 21 days [+17]

Hypersensitivity to Oleogel-S10 or any of its excipients [+12]

Status: Recruiting

Qualitative Study in Patients With Genodermatoses and Healthcare Professionals on Reproductive Counselling

The goal of this observational study is to understand the perspectives and needs of patients with genodermatoses and their partners who wish to have children, regarding their decision-making process and their consideration of reproductive options. Additionally, the investigators aim to investigate the level of knowledge and perspectives of healthcare professionals (such as clinical geneticists, dermatologists and other clinicians involved), and want to explore to what extent patients and their partners are well informed about these reproductive options. To achieve this, the investigators will conduct individual semi-structured qualitative interviews with participants affected by genodermatoses (and their partners) and with healthcare professionals.

Participants needed: 25
Trial details
Biological sex: AllType: ObservationalSponsor: Maastricht University Medical CenterUpdated: May 18, 2025Locations: 1
Eligibility criteria

Adult patients with genodermatosis (i.e, keratinisation disorders, skin fragilit... [+2]

Not being able to communicate verbally in Dutch or English