ContraFect Announces FDA Clearance Of CF-370 IND Application To Proceed With Phase 1 Clinical Study
Portfolio Pulse from Bill Haddad
ContraFect has received FDA clearance for its Investigational New Drug (IND) application for CF-370, allowing it to proceed with Phase 1 clinical trials.
October 16, 2023 | 11:31 am
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ContraFect's FDA clearance for CF-370 IND application could potentially boost its stock as it signifies progress in the company's drug development pipeline.
FDA clearance for an IND application is a significant milestone in drug development. It allows the company to proceed with clinical trials, which if successful, could lead to commercialization of the drug and potential revenue growth. This news could therefore be seen as a positive development by investors, potentially leading to an increase in ContraFect's stock price in the short term.
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