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SCYNEXIS Presents New Preclinical Data on Second Generation Fungerp SCY-247 at the 11th Congress on Trends in Medical Mycology (TIMM)

Key Takeaway: SCYNEXIS, Inc. announced the presentation of preclinical data on SCY-247, its second-generation antifungal candidate, at the 11th Congress on Trends in Medical Mycology. The data reveals SCY-247's potent in vitro activity against a broad range of fungal pathogens, including drug-resistant strains. Its favorable tissue distribution, including brain penetration, indicates potential for effective treatment of systemic fungal infections. Clinical studies for SCY-247 are planned to begin in the second half of 2024.
Price reaction · baseline $13.76 (2023-10-23 close) · hit after-hours · clean, no other SCYX news in the window
day 0 close · peak
-3.8%

Market Sentiment Analysis

POSITIVE FACTORS

  • SCY-247 shows potent broad-spectrum activity against various fungal pathogens.
  • The compound has demonstrated effective brain penetration and dose-dependent efficacy.
  • SCYNEXIS expects potential FDA designations that could accelerate its development.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+56%
120-day peak, hindsight
Typical move
12.1%
average across 3 past catalysts
Cash runway
~11 mo
Medium dilution risk
Lead asset
Ibrexafungerp
Phase 3 · Vulvovaginal Candidiasis

Full Press Release Details

JERSEY CITY, N.J., Oct. 24, 2023 (GLOBE NEWSWIRE) -- SCYNEXIS, Inc. (NASDAQ: SCYX), a biotechnology company pioneering innovative medicines to overcome and prevent difficult-to-treat and drug-resistant infections, today announced the presentation of preclinical data on its second generation fungerp candidate, SCY-247, against a broad panel of fungal pathogens. The analyses were presented by Mahmoud Ghannoum, Ph.D, Professor and Director Center for Medical Mycology, Case Western Reserve University, in an oral presentation titled, “SCY-247, a Second-generation IV/Oral Triterpenoid Antifungal: In Vitro Activity Against a Broad-spectrum of Fungal Pathogens, and Dose-dependent Tissue Distribution In Vivo” at the 11th Congress on Trends in Medical Mycology (TIMM) held in Athens Greece October 20-23, 2023.
“We are excited to see the progress in the development of this novel compound from the fungerp family,” said Dr. Martin Hoenigl, FECMM, Associate Professor of Translational Mycology at University of Graz, Austria and president of the European Confederation of Medical Mycology (ECMM). “With the growing concern over antifungal resistance and the increase in the number of vulnerable patients susceptible to deadly fungal infections, there is an urgent need to address current gaps in our armamentarium with new therapies, particularly potent and broad-spectrum antifungals with oral and IV formulations and low risk for drug-drug interactions.”
The preclinical study evaluated the activity of second-generation triterpenoid antifungal candidate SCY-247 against a range of fungal pathogens, including multi-drug resistant strains. Results illustrated the potent and broad-spectrum in vitro activity of SCY-247, including against a large array of yeasts, molds and dimorphic fungi. Results also demonstrated SCY-247’s extensive tissue distribution in mice, including brain penetration. Finally, SCY-247 demonstrated fungicidal activity against multi-drug resistant strains, including Candida albicans and Candida auris, as well as evidence of dose-dependent in vivo efficacy in a mouse model of invasive candidiasis.
SCY-247 is a second-generation antifungal compound from a novel class of structurally-distinct glucan synthase inhibitors, triterpenoids (fungerps), under development as a therapeutic option for systemic fungal diseases. The fungerps represent the first new class of antifungal compounds since 2001. These agents combine the well-established activity of glucan synthase inhibitors with the potential flexibility for oral and intravenous (IV) routes of administration. SCY-247 has demonstrated broad-spectrum antifungal activity, in vitro and in vivo, and SCYNEXIS anticipates that the U.S. Food and Drug Administration (FDA) may grant SCY-247 Qualified Infectious Disease Product (QIDP) and Fast Track designations for its IV and oral formulations. SCYNEXIS plans to begin clinical studies in the second half of 2024.
SCYNEXIS, Inc. (NASDAQ: SCYX) is a biotechnology company pioneering innovative medicines to help millions of patients worldwide overcome and prevent difficult-to-treat infections that are becoming increasingly drug-resistant. SCYNEXIS is developing the company’s proprietary antifungal platform, known as “fungerps”. Ibrexafungerp, the first representative of this novel class, has been licensed to GSK. The FDA approved BREXAFEMME® (ibrexafungerp tablets) in June 2021, for its first indication in vulvovaginal candidiasis (VVC), followed by a second indication in November 2022, for reduction in the incidence of recurrent VVC. Late-stage clinical investigation of ibrexafungerp for the treatment of life-threatening invasive fungal infections in hospitalized patients is ongoing. Additional antifungal assets from this novel class are currently in pre-clinical and discovery phase, including the compound SCY-247. For more information, visit www.scynexis.com.
Forward-Looking Statements
Statements contained in the last two sentences of the section “About SCY-247” in this press release are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, and are subject to risks and uncertainties, and actual results may differ materially from those expressed or implied by such forward-looking statements. For information regarding these risks and uncertainties, see SCYNEXIS' most recent Annual Report on Form 10-K filed on March 31, 2023, including under the caption "Risk Factors." These forward-looking statements contained in this press release speak only as of the date on which they were made. SCYNEXIS undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.

Frequently Asked Questions

What is SCY-247?

SCY-247 is a second-generation antifungal from the novel class of triterpenoids.

What pathogens does SCY-247 target?

It targets a broad range of fungal pathogens, including drug-resistant strains.

When will clinical studies for SCY-247 begin?

SCYNEXIS plans to initiate clinical studies in the second half of 2024.

What are the advantages of using SCY-247?

SCY-247 offers broad-spectrum activity with oral and IV administration options.

Is SCY-247 eligible for FDA designations?

Yes, SCY-247 may receive FDA's QIDP and Fast Track designations for its formulations.

Last updated: Oct 24, 2023