iRegene doses first US Parkinson’s patient, launches landmark MSA trial in China
The move follows encouraging Phase I data and a series of regulatory wins from the U.S. Food and Drug Administration
The move follows encouraging Phase I data and a series of regulatory wins from the U.S. Food and Drug Administration
The RMAT designation accelerates the development of regenerative medicine therapies for serious or life-threatening diseases
NouvNeu001 is the world’s first allogeneic iPSC-derived cell therapy for Parkinson’s disease to receive this designation
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