Safety and Efficacy of Ev.FV in Epidermolysis Bullosa Patients, A Randomized Clinical Trial, Phase 1 , 2

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

Epidermolysis bullosa (EB) is a hereditary disease of skin tissues that causes painful bleeding blisters in the skin and mucous membrane. The prevalence of this disease is 1 in 50,000. The severity of the disease varies depending on the type of disease and may even lead to death. This disease is caused by a genetic mutation in keratin or collagen, and its incidence is the same in all men and women of different human races. In these patients, the skin becomes extremely fragile and peels off with the slightest scratch. Many blisters are one of the most obvious symptoms of this disease. The possibility of skin cancer in people suffering from this disease is more than others. Nowadays, the preference of cell therapy methods is to use biological products produced by cells such as extracellular vesicles and mitochondria instead of stem cells. The use of Extracellular vesicles and engineered EVs as messenger carriers can introduce a new treatment method based on cell products for skin regeneration and as an alternative to cell therapy. Therefore, in this study, EV.FV will be applied topically to patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 35
Healthy Volunteers: f
View:

• DEB participants determined by electron microscopy, or genetic testing. Individuals with severe DEB (eg, RDEB patients with an absence of collagen VII) and milder forms of DEB (eg, RDEB patients with reduced levels of collagen VII) will be eligible.

• People with one or more active wounds (each between 10 and 50 square centimeters on the arms, legs or trunk.)

• Participants must be willing to comply with the requirements of the protocol and have consent to participate in the project.

• Participants must be negative in the urine drug screening visit.

Locations
Other Locations
Islamic Republic of Iran
Alzahra Hospital
RECRUITING
Isfahan
Contact Information
Primary
Leila Dehghani, Dr
l_dehghani2002@yahoo.com
36202020
Backup
Masoud Soleimani, Prof
soleimani.masoud@gmail.com
03136202020
Time Frame
Start Date: 2024-01-09
Estimated Completion Date: 2026-12-25
Participants
Target number of participants: 20
Treatments
Experimental: Treatment
Qualified patients who have confirmed chronic wounds (10-50cm2) are included in the study after completing the consent form
Sponsors
Leads: Isfahan University of Medical Sciences

This content was sourced from clinicaltrials.gov