The ThinkEquity Conference 2024
Logotype for Quince Therapeutics Inc

Quince Therapeutics (QNCX) The ThinkEquity Conference 2024 summary

Event summary combining transcript, slides, and related documents.

Logotype for Quince Therapeutics Inc

The ThinkEquity Conference 2024 summary

3 Feb, 2026

Clinical 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.

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