SCYNEXIS Doses First Participants in Phase 1 IV SCY-247 SAD/MAD Trial

Reuters

Feb 26

SCYNEXIS Doses First Participants in Phase 1 IV SCY-247 SAD/MAD Trial

SCYNEXIS Inc. announced that the first participants have been dosed in a Phase 1 single ascending dose and multiple ascending dose clinical trial evaluating an intravenous formulation of its second-generation triterpenoid antifungal candidate SCY-247. The study is assessing IV SCY-247 for development as a treatment for invasive candidiasis and as prophylaxis for invasive fungal disease. Results from this Phase 1 trial are expected to be reported in 2026; results have not yet been presented.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. SCYNEXIS Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202602260823PRIMZONEFULLFEED9662059) on February 26, 2026, and is solely responsible for the information contained therein.

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The study is assessing IV SCY-247 for development as a treatment for invasive candidiasis and as prophylaxis for invasive fungal disease. Results from this Phase 1 trial are expected to be reported in 2026; results have not yet been presented.\n      \n\n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. SCYNEXIS Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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