FDA Clearance Received to Complete Enrollment in REGAIN Recurrent GBM Trial and Addition of Two US Clinical Sites
Uzi Sofer, CEO of Alpha Tau, commented, “Glioblastoma is one of the most devastating diagnoses in oncology and is a core strategic indication for the Company. Since the fantastic interim results we released last month from our first three recurrent GBM treatments, clinicians have been overwhelmingly demanding that we keep treating patients as quickly as possible. This clearance, combined with the expansion to additional leading U.S. centers, hopefully brings us meaningfully closer to making Alpha DaRT a real option for these patients.”
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