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Coya Therapeutics (COYA) Q2 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Coya Therapeutics Inc

Q2 2026 earnings summary

11 Aug, 2026

Executive summary

  • Focused on developing therapies targeting regulatory T cell (Treg) dysfunction for neurodegenerative, autoimmune, and metabolic diseases, with lead asset COYA 302 in Phase 2 ALS trials and Fast Track Designation from the FDA.

  • Advanced lead program COYA 302 with ongoing enrollment in the ALSTARS Phase 2 ALS trial, on track for topline data in Q1 2027.

  • Initiation of a Phase 2 study in frontotemporal dementia (FTD) planned for 2H 2026.

  • Operations funded primarily through equity sales and collaboration payments; no product sales revenue to date.

  • Published supporting biomarker data and presented at major scientific meetings.

Financial highlights

  • Net loss was $6.6 million for Q2 2026, compared to $6.1 million in Q2 2025; net loss for the six months ended June 30, 2026 was $13.8 million, up from $13.4 million year-over-year.

  • Collaboration revenue was $0.2 million for Q2 2026 and $0.5 million for the six months, both related to R&D services under the DRL Development Agreement.

  • Research and development expenses increased to $5.0 million in Q2 2026 (from $3.7 million in Q2 2025), mainly due to advancement of COYA 302 ALS Phase 2 trial.

  • General and administrative expenses decreased to $2.3 million in Q2 2026 (from $2.9 million in Q2 2025), primarily due to lower professional services and compensation.

  • Cash and cash equivalents were $43.2 million as of June 30, 2026, sufficient to fund operations into 2H 2027.

Outlook and guidance

  • Existing cash is expected to fund operations into the second half of 2027, but substantial additional capital will be needed for continued development and commercialization.

  • Completion of ALSTARS Phase 2 trial enrollment and initiation of FTD Phase 2 study expected in 2H 2026.

  • Additional biomarker and single-cell proteomics data from ALS, FTD, and AD studies to be reported in 2H 2026.

  • Expenses and losses are expected to increase as clinical and preclinical programs advance and as commercialization activities ramp up.

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