Targeting Collagen VII Antibodies With IV IgG in Dystrophic Epidermolysis Bullosa

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

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6
Healthy Volunteers: f
View:

• Diagnosis of generalized Recessive dystrophic epidermolysis bullosa (RDEB) demonstrated by COL7A1 mutations.

• Diagnosis of EBA demonstrated by the presence of levels of serum C7 antibodies above the normal ELISA range

• Baseline skin blistering greater than 5% total body surface area

• 1 wound at least 20 cm\^2 able to be entirely treated with Vyjuvek weekly

• 1 wound at least 20 cm\^2 that has never been treated with Vyjuvek

• Ongoing VYJUVEK treatment.

Locations
United States
California
Stanford University
RECRUITING
Redwood City
Contact Information
Primary
Clinical Research Coordinator
cimino@stanford.edu
650-723-3439
Backup
Clinical Research Coordinator
kunju@stanford.edu
6507214902
Time Frame
Start Date: 2025-08-04
Estimated Completion Date: 2026-03-06
Participants
Target number of participants: 8
Treatments
Experimental: Intra-Personal Control
There is one arm of the study. First, each participant undergoes a 3-month observational period, during which they continue application of their prescribed Vyjuvek. After 3 months, they enter the treatment period, during which they continue their Vyjuvek application and, in addition, receive the IV IgG treatment.
Sponsors
Leads: M. Peter Marinkovich
Collaborators: Epidermolysis Bullosa Research Partnership

This content was sourced from clinicaltrials.gov

Similar Clinical Trials