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Recruiting No phase listed Observational

A Study to Assess the Incidence of Skin Cancers in Patients With Epidermolysis Bullosa Receiving Filsuvez

ClinicalTrials.gov ID: NCT06423573

Public ClinicalTrials.gov record NCT06423573. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 1, 2026, 8:52 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Long-term Non-interventional Study to Assess the Incidence of Skin Malignancies in Patients With Dystrophic and Junctional Epidermolysis Bullosa Receiving Treatment With Filsuvez

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

In patients with epidermolysis bullosa (EB), collagen does not form properly, so their skin is very fragile and blisters easily. Such patients are also at greatly increased risk of developing skin cancers. Filsuvez is a topical gel used to promote healing of skin lesions in patients with certain types of EB. In this observational study, patients with either dystrophic EB (DEB) or junctional EB (JEB) will receive standard of care treatment, whether Filsuvez or something else, and will be followed for a minimum of 3 years. The main purpose is to see if the use of Filsuvez affects the likelihood of developing skin malignancies in these patient populations.

Study identification

NCT ID
NCT06423573
Recruitment status
Recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
Chiesi Farmaceutici S.p.A.
Industry
Enrollment
170 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 18, 2024 (Actual)
Primary completion
Nov 30, 2031 (Estimated)
Completion
Aug 1, 2032 (Estimated)
Last update posted
Sep 28, 2026

2024 – 2032

United States locations

U.S. sites
6
U.S. states
6
U.S. cities
6
Facility City State ZIP Site status
Lucile Packard Children's Hospital Palo Alto California 94304 Not yet recruiting
UCHealth / Children's Hospital Colorado Aurora Colorado 80045 Not yet recruiting
UF College of Medicine Gainesville Florida 32606 Not yet recruiting
Cincinnati Children's Cincinnati Ohio 45229 Not yet recruiting
Childrens Hospital of Philadelphia Philadelphia Pennsylvania 19104 Not yet recruiting
Medical University of South Carolina Charleston South Carolina 29425 Not yet recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06423573, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 28, 2026 · Synced Oct 1, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06423573 live on ClinicalTrials.gov.

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