StemCyte, a subsidiary of StemCyte International, has secured approval from the US Food and Drug Administration for Regenecyte, a cord blood-derived stem cell therapy.
Regenecyte, an allogeneic hematopoietic stem cell therapy, is derived from human umbilical cord blood and is approved for unrelated donor hematopoietic progenitor cell transplants. The therapy is designed to reconstitute the hematopoietic and immune systems in patients with inherited, acquired, or treatment-related hematopoietic disorders.
In addition to Regenecyte, the firm is advancing Phase II clinical trials investigating cord blood-derived therapies for long COVID and acute stroke, alongside exploring potential treatments for aging-related diseases and chronic fatigue syndrome.
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