Quince Therapeutics (QNCX) The ThinkEquity Conference 2024 summary
Event summary combining transcript, slides, and related documents.
The ThinkEquity Conference 2024 summary
3 Feb, 2026Clinical program highlights
Pivotal Phase III NEAT trial of EryDex for ataxia-telangiectasia (A-T) is underway, with topline results expected in Q4 2025 and cash runway into early 2026.
The phase III study is risk-mitigated with FDA Special Protocol Assessment, Fast Track, and Orphan Drug Designation, enabling faster progress and cost savings.
The study focuses on 6- to 9-year-old patients, leveraging prior data showing efficacy in this subgroup.
An open-label extension and label expansion for older patients are underway.
Prior Phase 3 ATTEST study showed EryDex was well-tolerated and improved outcomes in A-T patients.
Technology and therapeutic approach
EryDex uses proprietary AIDE technology to encapsulate dexamethasone in autologous red blood cells, enabling monthly infusions with unique biodistribution and reduced steroid side effects.
Over 270 patients have received EryDex, with nearly 6,000 doses administered and no serious safety concerns or typical steroid side effects observed.
The device is CE marked in Europe, with IP protection extending globally to 2034 and in the U.S. to 2035.
The process is fully automated, takes 1.5 hours, and is designed for scalability and flexibility across therapeutic classes.
Over $100 million has been invested in AIDE technology development.
Market opportunity and commercial strategy
EryDex targets a $1+ billion global peak commercial opportunity for A-T, with an estimated 10,000 patients in the U.S., U.K., and major European countries.
No approved treatments exist for A-T, and EryDex has first-to-market potential with no known late-stage competition.
Pricing is benchmarked against Skyclarys ($370,000/year), with cost of goods under 1%.
Commercial rollout will begin in centers of excellence and infusion centers, with potential for mobile delivery in rural areas.
Plans include exploring partnerships, out-licensing opportunities, and potential out-licensing of ex-U.S. territories.
Latest events from Quince Therapeutics
- Phase III data for a chronic steroid therapy in rare disease expected Q4, with strong safety and market potential.QNCX
The Citizens JMP Life Sciences Conference 20253 Feb 2026 - EryDex's phase III trial targets a $1B+ rare disease market with broad expansion potential.QNCX
LD Micro Main Event XVII18 Jan 2026 - Biotech seeks up to $200M, including $75M at-the-market, to fund R&D and operations.QNCX
Registration Filing16 Dec 2025 - Biotech registers resale of 17.3M shares after $11.5M private placement to fund rare disease therapy.QNCX
Registration Filing16 Dec 2025 - Red blood cell-encapsulated steroid therapy nears pivotal data in AT, targeting major rare disease markets.QNCX
Oppenheimer 35th Annual Healthcare Life Sciences Conference (Virtual) 202516 Dec 2025 - eDSP nears pivotal phase III readout in AT, with strong safety, regulatory, and commercial momentum.QNCX
Investor Day 202514 Dec 2025 - eDSP offers a novel, safe corticosteroid therapy for A-T, targeting a billion-dollar rare disease market.QNCX
Investor Presentation8 Dec 2025 - Pivotal trial for a novel AT therapy targets 2024 NDA filing and broad U.S. patient access.QNCX
Piper Sandler 37th Annual Healthcare Conference4 Dec 2025 - Red blood cell-encapsulated steroid therapy for A-T nears pivotal trial results in late 2025.QNCX
Investor Update2 Dec 2025