Clinical trial of cell therapy developed by CZECRIN infrastructure for patients with “butterfly children” disease is ongoing at Brno University Hospital

Clinical Trials

28 November, 2022

Záhlaví

Clinical trial of cell therapy developed by CZECRIN infrastructure for patients with “butterfly children” disease is ongoing at Brno University Hospital

An academic clinical trial for patients with the rare congenital disease epidermolysis bullosa (EB), also known as “butterfly children” disease, has been initiated in collaboration between the CZECRIN infrastructure (MU Faculty of Medicine) and the University Hospital Brno. The clinical trial aims to test the drug’s safety and obtain the first information on how the cell therapy administered promotes the healing of chronic wounds. 

Drug was given to the first patient

A team of doctors and nurses is conducting the clinical trial from the Burns and Plastic Surgery Clinic of the Brno University Hospital and the EB Centre at the Children’s Dermatology Department of the Paediatric Clinic of the Brno University Hospital. In mid-October 2022, the drug was given to the first patient. After the necessary 24-hour observation, the man was discharged home from the hospital in good condition and will have regular follow-ups and repeat applications. He will be monitored in the study for one year. Three more patients will begin the treatment by the end of 2022 and early 2023. An initial safety analysis of the treatment will take place, and if the results are favourable, additional patients will be included in the study.

Cell therapy

The cell therapy drug consists of mesenchymal stromal cells (MSCs). These cells in the human body help repair damaged structures and regulate the exaggerated functions of the immune system. According to existing research, MSCs have healing potential in acute and chronic wounds of various origins. Experts from the Advanced Cell Immunotherapy Unit (ACIU) at the Institute of Pharmacology of the Faculty of Medicine (MUNI) have been working on the development of the product for several years, preparing the MSC medicine from fat tissue of healthy volunteers in a “clean room” (GMP) environment.

The above-mentioned clinical study is supported by the patient organization DEBRA CZ, z.ú.

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