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ACTIVE NOT RECRUITING
NCT06892639
PHASE3

Evaluation of D-Fi for the Treatment of Wounds Due to DEB

Sponsor: Castle Creek Biosciences, LLC.

View on ClinicalTrials.gov

Summary

The purpose of this study is to determine whether administration of D-Fi in addition to standard of care improves wound healing as compared to standard of care alone (control) in children, adolescents, and adults with Dystrophic Epidermolysis Bullosa.

Official title: Evaluation of Dabocemagene Autoficel (D-Fi; FCX-007; Genetically Modified Autologous Human Dermal Fibroblasts) for the Treatment of Wounds Due to Dystropic Epidermolysis Bullosa

Key Details

Gender

All

Age Range

2 Years - Any

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2025-03-27

Completion Date

2042-02

Last Updated

2026-03-13

Healthy Volunteers

No

Interventions

BIOLOGICAL

D-Fi

D-Fi is composed of fibroblasts isolated from the subject's skin biopsies which are genetically corrected with the full length COL7A1 gene encoding for type VII collagen.

Locations (4)

Stanford University School of Medicine, Dermatology

Redwood City, California, United States

Mission Dermatology

Santa Margarita, California, United States

Children's Hospital Colorado

Aurora, Colorado, United States

University of Massachusetts

Worcester, Massachusetts, United States