Logotype for Maze Therapeutics Inc

Maze Therapeutics (MAZE) Q1 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Maze Therapeutics Inc

Q1 2026 earnings summary

12 May, 2026

Executive summary

  • Advanced two clinical programs, MZE829 (APOL1-mediated kidney disease) and MZE782 (phenylketonuria and CKD), with positive Phase 2 and Phase 1 data, and plans for further trials in 2026 and 2027.

  • Positive topline data from Phase 2 HORIZON trial of MZE829 in broad AMKD, showing proof-of-concept and supporting advancement to pivotal trial; additional data expected late 2026 or early 2027.

  • Achieved a $20M milestone payment from Shionogi for dosing the first patient in a Phase 2 study of MZE001 for Pompe disease.

  • Reported a net loss of $24.2M for Q1 2026, an improvement from $32.8M in Q1 2025, driven by increased license revenue and higher R&D and G&A expenses.

  • Strong balance sheet with $528M in cash, cash equivalents, and marketable securities, including proceeds from a $150M offering and a $20M milestone payment.

Financial highlights

  • License revenue of $20.0M in Q1 2026, compared to none in Q1 2025, due to the Shionogi milestone.

  • Research and development expenses rose to $34.1M (up $6.6M year-over-year), mainly from increased headcount, stock-based compensation, and clinical trial activity.

  • General and administrative expenses increased to $12.4M (up $4.6M year-over-year), reflecting higher personnel and professional service costs.

  • Net loss per share improved to $0.45 in Q1 2026 from $1.15 in Q1 2025.

  • Cash, cash equivalents, and marketable securities totaled $362.9M as of March 31, 2026.

Outlook and guidance

  • Plans to continue Phase 2 enrollment for MZE829 and initiate Phase 2 trials for MZE782 in PKU and CKD in 2026, with topline data expected in 2027.

  • Cash runway expected to extend into 2029 based on current business plan and recent capital raise.

  • Pivotal trial for MZE829 in moderate AMKD without diabetes, including FSGS, planned for first half of 2027, pending regulatory feedback.

  • Expects research and development expenses to increase as clinical programs advance and pipeline expands.

  • Existing cash resources expected to fund operations for at least one year from the report date.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more