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CYTORA at The International MSA Congress Boston 2025: Prof. Sandu Pitaru, Co-founder, CSO,  VP R&D & Clin Affairs and Prof. Tanya Gurevich, KOL of MSA, presented interim results of the Phase I clinical study for treating patients with moderate and advanced Multiple System Atrophy (MSA) with hOMSC300.

10 May 2025

Prof. Sandu Pitaru, Co-founder, CSO, VP R&D & Clin Affairs and Prof. Tanya Gurevich, KOL of MSA presented the interim results of the Phase I clinical study for treating moderate and advanced Multiple System Atrophy (MSA) as well as preclinical results from a mouse model of MSA at the International MSA Congress in Boston 2025. The safety data collected to date demonstrate that intrathecal administration of hOMSC300, CYTORA’s investigational, allogeneic, off the shelf cell therapy, is safe. In addition, preliminary efficacy data suggest that hOMSC may be efficient as a disease modifying therapy in moderate stages of MSA.

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Cytora’s patented platform technology is based on the discovery of a novel and unique stem cell population in the human oral mucosa (hOMSC), the origin of which is the embryonic nervous system. hOMSC are endowed with properties of neural crest, neural and mesenchymal stem cells. Cytora’s products are allogeneic, off-the-shelf, easily scalable, with a very competitive cost of goods (COG). The products were found to be safe and effective in early phase clinical trials in two indications: Diabetic Foot Ulcers (DFU) and Multiple System Atrophy (MSA).

Our products have high potential for treating complicated multifactorial diseases such as chronic and neurodegenerative diseases, incurable wounds and autoimmune diseases.

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