EUCTR2020-002936-55-CZ
Active, not recruiting
Phase 1
Safety and Efficacy of Allogenic Adipose Tissue-derived Mesenchymal Stromal Cells in Patients with Epidermolysis Bullosa: Clinical Trial Phase I/II - MSC-EB
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Masarykova univerzita
- Enrollment
- 15
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Age \> 1 year (incl.)
- •2\) Clinical diagnosis of hereditary EB supported by histological diagnosis (electron microscopy, immunofluorescence antigen mapping) and DNA analysis
- •3\) The extent of the disease is at least 10% of the body surface
- •4\) Participants in a clinical trial of childbearing potential must agree to the use of prescribed contraceptive methods for the duration of the clinical study and for at least 6 months following the last dose of the study medication:
- •a) Women \- Proper use of a highly reliable method of contraception, ie combined hormonal contraception (in oral, vaginal or transdermal dosage form), gestagen hormonal contraception associated with ovulation inhibition (in oral or injectable dosage form), non\-hormonal intrauterine device or intrauterine device releasing hormones, or the presence of bilateral tubal occlusion, a partner's vasectomy, or adherence to sexual abstinence as part of the patient's normal lifestyle.
- •b) Men \- Adherence to sexual abstinence or the use of an adequate contraceptive method (ie condom) in case of sexual intercourse.
- •5\) Willingness and ability to adhere to restrictions in the care of study lesions and to adhere to the schedule of visits and examinations during the course of the study.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 11
- •F.1\.2 Adults (18\-64 years) yes
Exclusion Criteria
- •1\) Systemic infection or sepsis 7 days before MSC administration
- •2\) Treatment with blood transfusion (erythrocyte concentrate or whole blood transfusion) 7 days before MSC administration
- •3\) Clinical signs of infection in the study lesions 7 days before MSC administration
- •4\) Inability to tolerate repeated skin injections (especially in pediatric patients)
- •5\) History of basal cell or squamous cell carcinoma of the skin in the last 5 years
- •6\) History of other malignancies of any type at any time during life
- •7\) Severe lung disease that requires home oxygenation
- •8\) Severe kidney or liver disease
- •9\) Dilatation cardiomyopathy
- •10\) Life expectancy less than 90 days
Outcomes
Primary Outcomes
Not specified
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