COYA
Coya Therapeutics, Inc.5.83
-0.08-1.35%
Dec 16, 4:00:00 PM EST
Earnings Call Transcripts
This Quarter (Q1 '26)
No earnings call transcript available yet
Last Quarter (Q4 '25)
No earnings call transcript available
Key Stats
Market Cap
121.99MP/E (TTM)
-Basic EPS (TTM)
-1.11Dividend Yield
0%Recent Filings
8-K
FY2025 results: revenue up, loss widens
Coya Therapeutics reported FY2025 results on March 16, 2026, with collaboration revenue up to $7.9M from $3.6M, fueled by COYA 302 ALS and FTD milestones, yet net loss widened to $21.2M amid $16.7M R&D spend. Cash hit $46.8M after $23M public offering and $11.1M private placement, stretching runway to 2H 2027. ALSTARS Phase 2 trial enrolls now. Pipeline advances, but clinical risks loom.
10-K
FY2025 results
Coya Therapeutics posted FY2025 net loss of $21.2 million, up from $14.9 million in 2024, reflecting ramped R&D on Treg-enhancing biologics amid no revenue. Losses mounted quarterly with clinical milestones, yet cash runway stretches into H2 2027 post-January 2026's $11.1 million raise from Dr. Reddy's. Q4 2025 ignited momentum: FDA IND clearance for COYA 302 in ALS, dosing launched in ALSTARS Phase 2 trial. No decline in ALSFRS-R scores marked prior POC stability. Pipeline advanced with COYA 302 FTD IND and COYA 303 preclinical wins. Clinical delays could stall quarterly progress.
8-K
Coya raises $11.1M for COYA 302
Coya Therapeutics signed a securities purchase agreement on January 29, 2026, to sell 2,522,727 common shares at $4.40 each to Dr. Reddy's Labs ($10M) and Greenlight Capital ($1.1M), raising ~$11.1M gross before expenses. Closing expected January 30. Funds accelerate LD IL-2 tech transfer and manufacturing scale-up for COYA 302 commercial readiness. Cash runway holds into H2 2027.
8-K
Positive FTD study results
Coya Therapeutics announced positive proof-of-concept results from an investigator-initiated open-label study on January 8, 2026, testing low-dose IL-2 and CTLA4-Ig in 9 Frontotemporal Dementia patients over 22 weeks. Treg suppressive function and percentages surged significantly from week 2 and stayed elevated; MOCA scores held steady (13.5 to 14), CDR-FTLD showed no decline (4.8 to 5.5). Mild injection-site erythema was the sole common side effect. No serious adverse events.
ALDX
Aldeyra Therapeutics, Inc.
5.31+1.32
CERO
CERo Therapeutics Holdings, Inc
0.09-0.01
CGTX
Cognition Therapeutics, Inc.
1.52-0.08
COEP
Coeptis Therapeutics Holdings,
14.43-0.66
CUBT
CURATIVE BIOTECHNOLOGY INC.
0.01+0.00
CUE
Cue Biopharma, Inc.
0.41-0.05
SABS
SAB Biotherapeutics, Inc.
3.99-0.01
TNYA
Tenaya Therapeutics, Inc.
0.77-0.03
VYGR
Voyager Therapeutics, Inc.
4.42+0.06
XLO
Xilio Therapeutics, Inc.
0.65+0.00