Alpha Tau Receives FDA Approval To Begin Multi-Center Study Of Alpha DaRT For Immunocompromised Patients With Recurrent cSCC
Portfolio Pulse from Benzinga Newsdesk
Alpha Tau Medical has received FDA approval to start a multi-center study of its Alpha DaRT technology for treating immunocompromised patients with recurrent cutaneous squamous cell carcinoma (cSCC). This approval marks a significant step in the company's efforts to expand the use of its innovative cancer treatment technology.
September 20, 2024 | 12:31 pm
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Alpha Tau Medical's FDA approval for a multi-center study of Alpha DaRT in immunocompromised patients with recurrent cSCC is a significant regulatory milestone. This could enhance the company's market position and investor confidence.
The FDA approval is a critical regulatory milestone for Alpha Tau Medical, potentially leading to increased market confidence and future revenue growth. This development is likely to positively impact the stock price in the short term.
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