H.C. Wainwright 28th Annual Global Investment Conference
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Maze Therapeutics (MAZE) H.C. Wainwright 28th Annual Global Investment Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Maze Therapeutics Inc

H.C. Wainwright 28th Annual Global Investment Conference summary

15 Sep, 2026

Pipeline overview and upcoming catalysts

  • Three clinical programs are in development: MZE829 for APOL1-mediated kidney disease (AMKD), MZE782 for PKU, and MZE782 for chronic kidney disease (CKD), all supported by a genetics-driven platform.

  • MZE829 is in phase II (HORIZON study) with final data expected end of this year or early next; a pivotal program is planned for the first half of next year.

  • MZE782 for PKU has just started a phase II trial (CIPheR), with top-line data expected in 2027.

  • MZE782 for CKD is set to begin phase II in the first half of next year.

  • All programs are small molecules with full rights retained.

HORIZON study insights and AMKD landscape

  • Initial HORIZON data showed a 36% average uACR reduction and a 50% response rate across AMKD subgroups, with FSGS patients showing a 62% reduction.

  • The study includes FSGS, diabetic, and hypertensive non-diabetic AMKD patients, aiming for 10–15 patients per subgroup in the final data.

  • The 30% uACR reduction is considered a meaningful clinical benchmark, though lower reductions may be significant in diabetic cohorts.

  • HORIZON design was intentionally broad to address the full spectrum of AMKD, reflecting biological rationale and unmet need.

  • Recent protocol tweaks lowered the uACR enrollment threshold and capped FSGS enrollment to balance subgroups.

Competitive landscape and regulatory considerations

  • There is significant unmet need in AMKD, with an estimated 250,000 U.S. patients potentially benefiting from APOL1 inhibitors.

  • The field is awaiting recommendations from the PARSOL Shield initiative, which may define surrogate endpoints and accelerate development.

  • The company is monitoring competitor trials (AMPLITUDE, Vertex) and expects a surge in clinical data in the next 12–18 months.

  • Feedback from KOLs suggests a preference for broad pivotal trials with subgroup analyses rather than separate cohorts.

  • A go-it-alone commercialization strategy is being considered, but partnerships remain an option.

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