8-K current report · filed Aug 17, 2026

Maze Therapeutics, Inc. (MAZE) 8-K Current Report: August 17, 2026

Item 5.02Item 7.01Item EX-99.1MAZE overview

Short answer

Maze Therapeutics, Inc. (MAZE) filed an 8-K current report with the SEC on August 17, 2026 reporting Item 5.02 (Departure/Election of Directors or Officers), Item 7.01 (Regulation FD Disclosure), Item EX-99.1 (Exhibit EX-99.1). Board additions: Paula A. Johnson and Sophie Kornowski appointed as Class III and Class I directors, respectively.

Maze Therapeutics, Inc. 8-K event analysis

AI summary of each reported item and its exhibits

Item 5.02 · Departure/Election of Directors or Officers

  • Board additions: Paula A. Johnson and Sophie Kornowski appointed as Class III and Class I directors, respectively
  • Dr. Kornowski joins audit and compensation committees, strengthening biopharma, investment and business-development expertise
  • Dr. Johnson joins nominating and corporate governance committee, adding academic medicine and public-health leadership
  • Each director receives pro rata $40,000 annual cash retainer plus committee retainers and options for 36,000 shares
  • Board class realignment changes Nancy Andrews to Class II and Hervé Hoppenot to Class III without reducing board continuity

Item 7.01 · Regulation FD Disclosure

  • Exhibit 99.1 furnished under Regulation FD, not treated as filed under Exchange Act Section 18
  • Exhibit excluded from Securities Act Sections 11 and 12(a)(2) liability
  • Exhibit not incorporated by reference into other SEC filings unless expressly stated

Item EX-99.1 · Exhibit EX-99.1

  • Paula Johnson and Sophie Kornowski appointed to Maze’s Board, strengthening clinical, biopharmaceutical, partnering, and M&A expertise
  • MZE829 additional AMKD data expected in late 2026 or early 2027
  • Initial MZE782 data expected in 2027, with additional trial initiations for both molecules next year
  • Board expansion supports Maze’s transition toward late-stage clinical development and pre-commercial planning
  • Pipeline execution remains dependent on clinical results, regulatory approvals, and funding availability

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