King's College London, Intercytex and Debra begin Phase II trial with ICX-RHY in patients with severe genetic skin disorder
The placebo controlled trial will involve 20 RDEB patients. It will be led by Professor John McGrath, Professor of Molecular Dermatology at King’s College London and Honorary Consultant Dermatologist at Guy’s and St Thomas’ NHS Foundation Trust, London, who will administer a single series of ICX-RHY injections or placebo around the margins of several selected skin erosions. The injections will take place at the Clinical Research Facilities at Guy’s Hospital. Patients will then be assessed initially over a three month period to measure end points including time to wound closure, wound recurrence and erosion pain. The trial, which is scheduled for completion early in the autumn, is funded jointly by Intercytex, The Technology Strategy Board and DEBRA.
Professor McGrath has already used ICX-RHY successfully to treat 14 EB patients on a compassionate use basis. Commenting on the start of the trial, Prof McGrath said ‘Finding out whether a new treatment can help people with EB heal their wounds faster makes this an important clinical trial. We plan to test cells called “fibroblasts” to see if injection into the skin affects wound healing. The trial represents a significant step forward in taking research from the laboratory to the clinic.’
One in 227 people have a defective gene that causes EB and the disease affects around 1 in 17,000 live births. It is estimated that there are half a million sufferers world wide and 5,000 people with EB in the UK. RDEB is one of the more severe, debilitating forms of the disease, with a prevalence of around 2 in 100,000.
ICX-RHY is a suspension of human dermal fibroblasts (HDFs, which are naturally derived skin cells) in cell storage medium, for injection into the skin. The newly introduced HDFs are thought to repair the extracellular matrix to improve skin structure and function.
ICX-RHY is designated as one of the first Advanced Therapy Medicinal Products (ATMP) by the European Medical Agency and has already been used in clinical trials and compassionate use programmes in over 100 patients in a variety of indications.
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