Epidermolysis Bullosa
Conditions
Keywords
epidermolysis bullosa, chronic wound, wound healing, dermal repair, fibroblasts, Dermagraft
Brief summary
The purpose of this study is to evaluate the efficacy and safety of ABH001 in the treatment of patients with epidermolysis bullosa who have wounds that are not healing. It is hypothesized that ABH001 may initiate and continue wound healing in patients with epidermolysis bullosa.
Interventions
BIOLOGICALABH001
ABH001 applications topically every 4 weeks (±1 week) with protocol-specified dressings until wound healed or up to 44 weeks
OTHERControl wound treatment
Control wound care with protocol-specified dressings every 4 weeks (±1 week) up to 20 weeks with optional cross-over to ABH001 for additional 20 weeks
Sponsors
Shire Regenerative Medicine, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
1. The subject or legal guardian must have read, understood and signed an Institutional Review Board/Ethics Committee (IRB/EC) approved Informed Consent or Assent Form and must be able to and willing to follow study procedures and instructions 2. Male and female subjects. 3. Stable nutritional status. 4. Subjects with a confirmed diagnosis of generalized Epidermolysis Bullosa (EB) 5. Cutaneous wounds meeting the following criteria: 1. Anatomical location: arms, legs, thorax, or back above the waistline and below the neck. 2. Documented age (duration) of the wound(s). 3. One or more wounds capable of potentially meeting the following wound selection criteria at the end of the observation period: i. Two clinically non-infected cutaneous wounds with no clinically meaningful change in wound size during the observation period. ii. Two matched wounds. 6. Negative urine pregnancy test for women of child-bearing potential. 7. Female subjects of childbearing potential and male subjects of procreative capacity must agree to use an effective method of contraception.
Exclusion criteria
1. Pregnant or nursing women. 2. Diagnosis of non-genetic generalized EB. 3. Localized, active clinical infection of study wounds. 4. Diseases or conditions that could interfere with the assessment of safety and efficacy of the study treatment and compliance of the subject with study visits/procedures. 5. Known allergy to bovine products. 6. Known allergy to silver products. 7. Systemic infection at the time of enrolment in the study. 8. Currently receiving or have received oral steroid therapy within the previous 4 weeks. 9. Taking, or have participated in other clinical studies involving gene therapy, stem cell therapy, recombinant DNA/protein therapy. 10. Received ABH001, or other biologic or cell therapy for the treatment of EB in the study wound sites within the previous 3 months. 11. Hypersensitivity to any of the therapeutic agents. 12. History of malignant skin disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in wound surface area | 24 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Patient global impression of change (PGIC) | 24 weeks |
| Clinician global impression of change (CGIC) | 24 weeks |
| Proportion of subjects achieving reduction in wound surface area | 24 weeks |
| Change in wound pain and wound itch | 24 weeks |
| Durability of wound healing | 24 weeks |
| Incidence, relatedness and severity of adverse events | Up to 48 Weeks |
| Time to reduction of wound surface area and duration of reduction | 24 weeks |
Countries
Austria, Canada, France, Germany, Poland, Portugal, Spain, United States
Outcome results
None listed