GlaxoSmithKline (GSK) has selected MolMed to develop a production process for an experimental gene therapy for adenosine deaminase deficiency - severe combined immune deficiency (ADA-SCID).
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As per the terms of the agreement, GSK is responsible to pay up to EUR5.5m to MolMed in revenues for a term of two-year.
Developed by the San Raffaele Telethon Institute for Gene Therapy (HSR-TIGET), the gene therapy is in late stage clinical trials and was in-licensed by GSK to develop and commercialize the therapy.
MolMed chairman and CEO Claudio Bordignon said the company has expertise and know-how in the field of gene and cell therapy and this agreement with GSK is an important step on the way to provide gene therapy for patients with rare diseases.
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