SCYNEXIS patent for triterpenoid antifungals treating Pneumocystis pneumonia
Summary
The USPTO issued patent US12594266B2 to SCYNEXIS, INC. on April 7, 2026, covering eufumafungin derivative triterpenoid antifungal compounds and their use in treating or preventing Pneumocystis pneumonia (PCP). The patent includes 16 claims encompassing the compound structures, pharmaceutical compositions, and methods of treatment.
What changed
The USPTO granted patent US12594266B2 to SCYNEXIS, INC. for triterpenoid antifungal compounds derived from eufumafungin, which demonstrate unexpected efficacy against Pneumocystis spp. and can reduce lung burden of both cyst and trophic fungal forms. The compounds function as (1,3)-β-D-glucan synthesis inhibitors with potent in vivo activity, adequate lung tissue penetration, and favorable tolerability profiles. The 16-claim patent covers the compound structures, pharmaceutical formulations, and methods of use for treating or preventing PCP.
Affected parties including pharmaceutical companies, drug manufacturers, and researchers developing antifungal therapies should monitor this intellectual property grant as it may restrict freedom to operate in the PCP antifungal treatment space. Generic or biosimilar developers seeking to commercialize triterpenoid-based antifungals for Pneumocystis pneumonia will need to evaluate licensing options or design-around strategies to avoid infringing the granted claims.
What to do next
- Monitor patent portfolio for newly granted pharmaceutical patents
- Review patent claims for potential infringement on antifungal treatments
- Assess commercial opportunities for licensed or developed PCP therapies
Source document (simplified)
Triterpenoid antifungals for the treatment or prevention of Pneumocystis spp. pneumonia
Grant US12594266B2 Kind: B2 Apr 07, 2026
Assignee
SCYNEXIS, INC.
Inventors
David A. Angulo Gonzalez, Stephen Andrew Barat
Abstract
Eufumafungin derivative triterpenoid antifungal compounds are used to treat and/or prevent Pneumocystis pneumonia (PCP) due to their unexpected efficacy against Pneumocystis spp. including their ability to reduce the lung burden of cyst and trophic forms of this fungi. The enfumafungin derivative triterpenoids (or pharmaceutically acceptable salts or hydrates thereof) are inhibitors of (1,3)-β-D-glucan synthesis and are useful in the treatment and/or prevention of PCP since they demonstrate potent activity against Pneumocystis spp. in in vivo models, exhibit adequate tissue penetration into lungs, and are well tolerated.
CPC Classifications
A61K 31/4439 A61P 31/10 A61P 11/00
Filing Date
2020-02-25
Application No.
17432926
Claims
16
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