HUMA

Humacyte Inc
NASDAQHEALTHCAREBIOTECHNOLOGY

Key Statistics

Market Cap
$170.06M
P/E Ratio
EPS
$-0.63
Beta
2.52
52W High
$2.75
52W Low
$0.55
50-Day MA
$0.92
200-Day MA
$1.06
Dividend Yield
Profit Margin
0.00%
Forward P/E
35.84
PEG Ratio

About Humacyte Inc

Humacyte Inc (HUMA) is a groundbreaking biotechnology firm at the forefront of vascular and regenerative medicine, specializing in the development of human acellular vessels (HAVs). These innovative, off-the-shelf products are designed to meet pressing needs in vascular reconstruction and chronic disease management, improving patient outcomes and potentially reducing healthcare expenses. Leveraging its advanced technology platform, Humacyte is strategically positioned to drive innovation in transplantation and tissue engineering, thereby cementing its status as a transformative leader within the rapidly evolving landscape of medical therapies.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)$2.02M
Gross Profit (TTM)$-81.72M
EBITDA$-105.19M
Operating Margin-5704.00%
Return on Equity-409.50%
Return on Assets-51.50%
Revenue/Share (TTM)$0.01
Book Value$0.05
Price-to-Book15.74
Price-to-Sales (TTM)84.36
EV/Revenue99.39
EV/EBITDA4.34
Quarterly Earnings Growth (YoY)0.00%
Quarterly Revenue Growth (YoY)-4.30%
Shares Outstanding$269.64M
Float$196.13M
% Insiders7.51%
% Institutions22.30%

Historical Volatility

HV 10-Day
63.02%
HV 20-Day
81.62%
HV 30-Day
110.32%
HV 60-Day
126.47%
HV Rank

Volatility is currently contracting

Analyst Ratings

Consensus ($2.05 target)
1
Strong Buy
3
Buy
1
Hold

Latest News

Humacyte Announces FDA Acceptance of IND for First-In-Human Clinical Study of CTEV for Coronary Artery Bypass Grafting

– Phase 2a study of CTEV in coronary artery bypass grafting (CABG) is expected to start this quarter – – Progression of CTEV into human study supported by positive preclinical results presented at multiple scientific meetings and in a recent publication – DURHAM, N.C., July 27, 2026 (GLOBE NEWSWIRE) -- Humacyte, Inc. (Nasdaq: HUMA), a clinical-stage biotechnology platform company developing universally implantable, bioengineered human tissue at commercial scale, announced that the Food and Drug Administration (FDA) has accepted its Investigational New Drug (IND) application for a first-in-human clinical study of the coronary tissue engineered vessel (CTEV) in coronary artery bypass grafting (CABG).

GlobeNewsWire7/27/2026Neutral

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Data last updated: 7/29/2026