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Clinical Trials/EUCTR2020-002936-55-CZ
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

Masarykova univerzita0 sites15 target enrollmentAugust 3, 2020

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.

Registry
who.int
Start Date
August 3, 2020
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

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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