Coya Therapeutics

COYA · NASDAQ

$4.21+$0.01 (+0.24%)TodayMarket closed ·
Prev close $4.20

COYA analyst rating

BuyConsensus of 5 analysts over the last 12 months. 100% rate it a buy.
  • Strong buy0
  • Buy5
  • Hold0
  • Underperform0
  • Sell0

12-month price target · 8 analysts

Average $15.47 (+267.5% upside)

Low
$12.12
Now
$4.21
High
$18.90

Upgrades and downgrades

The latest rating actions, newest first

COYA analyst upgrades, downgrades and rating actions
FirmDateActionRating
BTIGSep 15, 2026MaintainsBuy
Roth CapitalAug 24, 2026MaintainsBuy
Chardan CapitalAug 12, 2026MaintainsBuy
Chardan CapitalJun 12, 2026MaintainsBuy
Roth CapitalJun 5, 2026InitiatesBuy
D. Boral CapitalApr 10, 2026MaintainsBuy
HC Wainwright & Co.Mar 23, 2026MaintainsBuy
D. Boral CapitalMar 19, 2026MaintainsBuy
Chardan CapitalMar 16, 2026MaintainsBuy
D. Boral CapitalMar 16, 2026MaintainsBuy

The case for and against

Updated Oct 21, 2026

Bull case

Coya Therapeutics is supported by a compelling Treg-modulation thesis that is mechanistically straightforward, backed by validated biologics, and increasingly validated by data showing deep immunomodulation, positive biomarkers, and safety across ALS and FTD. The FDA’s Fast Track designation for COYA-302 in ALS, combined with advancing ALSTARS milestones and top-line data expected in 1Q27, strengthens the case that the program could deliver clinically meaningful ALSFRS-R and mortality benefit in a high-unmet-need setting. Financially, the company’s cash runway guidance into 2H27, with $43.2M at June 30, reduces near-term funding risk while its pipeline breadth, including COYA-303, adds additional upside optionality.

Bear case

Coya Therapeutics is a clinical-stage biotech with no revenue-generating products, so its valuation depends heavily on unproven pipeline success while operating expenses and cash burn continue to rise, including $7.3 million in 2Q26 and a net loss of $6.6 million, or $(0.28) per share. The company’s R&D spending increased 37% to $5.0 million due largely to the COYA 302 ALS phase II trial, yet the text highlights substantial clinical, regulatory, reimbursement, and commercialization risk, any of which could impair program value. It also faces meaningful dilution risk because management expects future debt or equity financing, while intense competition and uncertain patent protection could leave its Treg-based therapies vulnerable even if development advances.

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