TNYA Tenaya Therapeutics, Inc. logo

TNYA Tenaya Therapeutics, Inc.

Healthcare
$0.77-2.22%ClosedMarket Cap: $128.7M

As of 2026-05-25

Valuation

View Details

P/E (TTM)

PEG

P/B

1.11

P/S

572.01

EV/EBITDA

-0.75

DCF Value

$0.57

FCF Yield

-50.2%

Div Yield

0.0%

Margins & Returns

Gross Margin

144.9%

Operating Margin

-38159.1%

Net Margin

-36891.1%

ROE

-80.6%

ROA

-61.5%

ROIC

-70.7%

Financials

View All
PeriodRevenueNet IncomeEPS
Q1 null$225.0K$-19.3M$
Q4 null$0.00$-20.2M$
FY null$0.00$-90.6M$
Q3 null$0.00$-20.3M$

Analyst Ratings

View All

Consensus

Buy

Target (Consensus)

$2.33

Target (Median)

$2.00

Target Range

$2.00 - $3.00

2 Strong Buy6 Buy0 Hold0 Sell0 Strong Sell
Chardan CapitalBuy
2026-03-12
Canaccord GenuityBuy
2025-12-18
Chardan CapitalBuy
2025-12-12
HC Wainwright & Co.Buy
2025-12-12
Chardan CapitalBuy
2025-11-10

Trading Activity

Insider Trades

View All
Tingley Whittemoreofficer: Chief Medical Officer
SellTue May 19
Higa Tomohiroofficer: SVP, Finance
SellTue May 19
Ali Farazdirector, officer: Chief Executive Officer
SellTue May 19
COLUMN GROUP III GP, LP10 percent owner
SellThu Feb 26
COLUMN GROUP III GP, LP10 percent owner
SellThu Feb 26

Company Info

Sector

Healthcare

Industry

Biotechnology

Country

US

Exchange

Beta

2.77

Tenaya Therapeutics, Inc., a biotechnology company, discovers, develops, and delivers therapies for heart disease in the United States. It develops its products through cellular regeneration, gene therapy, and precision medicine platforms. The company is developing TN-201, an adeno-associated virus (AAV)-based gene therapy to address genetic hypertrophic cardiomyopathy (gHCM) caused by haploinsufficient myosin binding protein C3 (MYBPC3) gene mutations; and TN-301, a small molecule inhibitor of histone deacetylase 6 (HDAC6i) for use in heart failure with preserved ejection fraction (HFpEF) and genetic dilated cardiomyopathy (gDCM). It is also developing TN-401, an AAV-based gene therapy that addresses genetic arrhythmogenic right ventricular cardiomyopathy (gARVC) caused by plakophilin 2 (PKP2) gene mutations; an AAV-based gene therapy designed to deliver the dwarf open reading frame (DWORF) gene in the heart for DCM; and Reprogramming program, an AAV-based approach for cardiac regeneration to replace heart cells lost in patients experiencing heart failure due to prior myocardial infarction. The company was incorporated in 2016 and is headquartered in South San Francisco, California.

Peers