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Aura Biosciences Reports Third Quarter 2026 Financial Results and Recent Business Highlights

  • Phase 3 CoMpass trial for bel-sar in early choroidal melanoma is fully enrolled with 108 participants, all of whom have completed treatment visits.
  • The CoMpass trial is on track to deliver topline data from the 15-month primary endpoint in the second half of 2027.
  • The trial is conducted under a Special Protocol Assessment (SPA) agreement with the FDA to support a potential Biologics License Application.
  • Aura Biosciences established a relationship with an industry-leading CDMO to secure designated manufacturing capacity for bel-sar.
  • An investor and analyst virtual event regarding early choroidal melanoma is scheduled for December 8, 2026.
  • Aura expects its cash, cash equivalents, and marketable securities of $297.2 million to fund operations into the first half of 2029.
  • Research and development expenses for the three months ended September 30, 2026, were $24.7 million, up from $22.2 million in the prior year period.
  • General and administrative expenses increased to $10.3 million for the quarter ended September 30, 2026, driven by $4.5 million in restructuring charges.
  • Net loss for the three months ended September 30, 2026, was $32.1 million compared to $26.1 million in the same period of 2025.
  • CEO Natalie Holles will participate in the Stifel 2026 Healthcare Conference on November 10, 2026, & the 9th Annual Evercore Healthcare Conference on December 1, 2026.
Company
Aura Biosciences, Inc.
Keywords
Nasdaq:AURA, Aura Biosciences, Inc.