SCYNEXIS (SCYX) Corporate presentation summary
Event summary combining transcript, slides, and related documents.
Corporate presentation summary
9 Nov, 2026Portfolio strategy
Portfolio targets the underlying biology of severe rare diseases, led by SCY-770 for ADPKD and SCY-247 for invasive fungal infections; BREXAFEMME is licensed to GSK.
Pipeline includes oral and IV SCY-247, preclinical fungerp analogs for resistant fungi, and approved ibrexafungerp tablets for VVC and recurrent VVC, partnered with GSK.
ADPKD opportunity and SCY-770
ADPKD affects >140K U.S. patients, with 6K new cases annually; 50% reach end-stage kidney disease by age 60. Jynarque had $1.5B in 2024 U.S. sales and ~11K U.S. patients.
SCY-770 is a first-in-class, selective oral direct AMPK activator with FDA Orphan Drug Designation; ~300 participants have been exposed across 9 clinical studies.
Phase 1 enrolled 25 healthy participants across three cohorts; SCY-770 was well tolerated at all doses, with loose stools the most common adverse event, and achieved the exposure target for efficacy.
Phase 2 proof-of-concept study in ADPKD is planned to start Q4 2026; interim analysis is expected Q4 2027, with study completion planned for 2H 2028.
Development plan anticipates potential accelerated FDA approval based on htTKV, followed by full approval based on eGFR; a single Phase 3 study is anticipated for approval.
SCY-247 and fungal infections
SCY-247 is a next-generation fungerp for invasive fungal infections, with oral and IV formulations, broad-spectrum fungicidal activity, tissue distribution, low DDI risk and favorable safety in ~148 clinical trial participants.
Oral and IV Phase 1 studies are complete; Phase 2 initiation is expected in 2027. SCY-247 has QIDP, Fast Track and Orphan Drug designations.
BARDA contract provides up to $214M if all options are exercised, including ~$18.5M in base-period funding, to support development through NDA submission without equity dilution.
U.S. invasive candidiasis market includes ~70K cases treated annually and a 20–40% mortality rate; estimated commercial opportunity for invasive fungal disease exceeds $700M annually.
Latest events from SCYNEXIS
- SCY-770 and BARDA-backed SCY-247 advance toward Phase II with runway into 2029.SCYX
3rd Annual Guggenheim Healthcare Innovation Conference - SCY-770 enters ADPKD Phase 2 as SCY-247 advances with up to $214M in BARDA support.SCYX
Corporate presentation - A $200 million shelf backs a clinical pipeline facing funding and development risks.SCYX
Registration filing - Clinical progress and BARDA funding support Phase 2 plans, with runway into 2029.SCYX
Q3 2026 - SCY-770 advances toward ADPKD proof-of-concept, with cash runway into 2029.SCYX
Corporate presentation - Phase II trial of SCY-770 for ADPKD to launch by year-end, targeting major unmet need.SCYX
12th Annual Cantor Fitzgerald Global Healthcare Conference - Q2 2026 net income was $7.4M, with strong cash reserves and key clinical milestones ahead.SCYX
Q2 2026 - All six proxy proposals were approved with no shareholder questions submitted.SCYX
AGM 2026 - Shareholders approved a reverse stock split and reduction of authorized shares.SCYX
EGM 2026