Targeting the Underlying Biology of Severe Rare Diseases

SCYNEXIS is a clinical-stage biotechnology company developing differentiated therapies for severe rare diseases, led by SCY-770 for autosomal dominant polycystic kidney disease (ADPKD) and SCY-247 for the treatment and prevention of serious fungal infections, addressing significant unmet needs for patients with limited treatment options.

Targeting the Underlying Biology of Severe Rare Diseases

SCYNEXIS is a clinical-stage biotechnology company developing differentiated therapies for severe rare diseases, led by SCY-770 for autosomal dominant polycystic kidney disease (ADPKD) and SCY-247 for the treatment and prevention of serious fungal infections, addressing significant unmet needs for patients with limited treatment options.

Validated Science. Disciplined Execution.

Our strategy is built on advancing programs with validated mechanisms, well-understood regulatory pathways, and clear potential to improve patient outcomes. Following the successful development and FDA approval of ibrexafungerp (BREXAFEMME®), now licensed to GSK, we are focused on developing innovative therapies for patients facing serious and underserved diseases.

Years Advancing Innovation
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Clinical-Stage Programs
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FDA-Approved Medicine
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Focused on Areas of Greatest Need

Our pipeline targets diseases where patients continue to face limited treatment options, including autosomal dominant polycystic kidney disease (ADPKD) and invasive fungal infections, where significant unmet medical need remains.

RARE KIDNEY DISEASE

ADPKD

A progressive inherited disease in which cyst growth drives declining kidney function, affecting approximately 140,000 diagnosed patients in the United States. SCYNEXIS is developing SCY-770, a first-in-class direct AMPK activator designed to address the metabolic biology underlying cyst formation.

INFECTIOUS DISEASE

Invasive Fungal Infections

Life-threatening fungal infections continue to present significant treatment challenges as resistance to existing therapies increases. SCYNEXIS is advancing next-generation antifungals with a differentiated mechanism and both oral and intravenous formulations, designed to expand treatment options for the treatment and prevention of serious fungal infections.

Two Clinical Programs. Multiple Opportunities.

Our portfolio includes SCY-770, a Phase 2 ready program targeting the underlying biology of autosomal dominant polycystic kidney disease (ADPKD), and SCY-247, a next-generation antifungal designed to address resistant fungal pathogens.

Complementary to these programs are additional antifungals in our preclinical portfolio; ibrexafungerp, an FDA-approved medicine developed by SCYNEXIS and now partnered with GSK; and the potential for SCY-770 to be developed for multiple other indications.

Clinical Development

SCY-770

Rare Kidney Disease (ADPKD)

A first-in-class direct AMPK activator developed to address the metabolic biology underlying cyst growth in autosomal dominant polycystic kidney disease.

Clinical Development

SCY-247

Next-Generation Antifungal Therapy

A second-generation fungerp in development for oral and intravenous treatment and prevention of serious and difficult-to-treat fungal infections.

Preclinical Research

Fungerp Analogs

Expanding the Antifungal Platform

Structurally distinct antifungal compounds advancing the next generation of the fungerp platform.

Approved & Licensed

BREXAFEMME®

Approved & Partnered Therapy

The first approved medicine from the Fungerp platform, demonstrating SCYNEXIS’ ability to advance innovative therapies through regulatory approval. GSK holds rights in most major markets, with an anticipated product relaunch expected to further demonstrate the long-term commercial value of the Fungerp platform.

Collaboration That Extends Our Reach