Humacyte, Inc.

Humacyte, Inc.

HUMAW
Humacyte, Inc.US flagNASDAQ Global Select
0.06
USD
-0.01
- -
66.20MMarket Cap
Humacyte, Inc.
HUMAW
(NASDAQ Global Select)

Recent

price

0.06

P/E

ratio

- -

div

yld

- -

ROIC.AI

2020
2021
2022
2023
2024
2025
TTM
FRC
- -
- -
- -
- -
- -
- -
- -
Revenue per Share
- -
- -
- -
- -
- -
- -
- -
Basic EPS, GAAP
- -
- -
- -
- -
- -
- -
- -
Free Cash Flow per Basic Share
- -
- -
- -
- -
- -
- -
- -
Dividend per Share
- -
- -
- -
- -
- -
- -
- -
Book Value per Share
- -
- -
- -
- -
- -
- -
- -
Tangible Book Value per Share
- -
- -
- -
- -
- -
- -
- -
Basic Weighted Avg Shares
- -
- -
- -
- -
- -
2
2
Sales/Revenue/Turnover
- -
- -
- -
- -
- -
-5,306.04
-5,649.21
Operating Margin (%)
8
8
8
8
7
7
7
Depreciation Expense
-67
-26
-12
-111
-149
-41
-98
Net Income, GAAP
- -
- -
- -
- -
- -
- -
- -
Effective Tax Rate (%)
- -
- -
- -
- -
- -
-2,003.58
-4,840.82
Profit Margin (%)
30
218
135
65
28
49
47
Working Capital
25
49
39
16
14
62
63
LT Debt
-350
122
117
14
-53
3
12
Total Equity
- -
- -
- -
- -
- -
- -
- -
Return on Invested Capital (%)
- -
- -
- -
- -
- -
- -
- -
Return on Capital (%)
- -
- -
- -
- -
- -
- -
- -
Return on Common Equity (%)

Capital Structure

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
ST Debt
3
2
2
LT Borrowings
- -
35
36
LT Finance Leases
27
27
28
Preferred Equity and Hybrid Capital
- -
- -
- -
Shares Outstanding
159
193
222
Market Capitalization
- -
- -
- -

Working Capital

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
Total Current Assets
41
68
64
Cash, Cash Equivalents & STI
19
50
49
Accounts Receivable, Net
1
- -
- -
Inventories
18
14
10
Total Current Liabilities
26
18
16
Payables & Accruals
14
9
14
ST Debt
3
2
2
Deferred Revenue
- -
- -
- -

Growth Rates

FRC

in mil. unless spec.

(avg. rate of change)

10 years
5 years
1 year
Total Equity
- -
-164.46%
-105.9%
Free Cash Flow
- -
15.44%
6.25%
Net Income, GAAP
- -
134.5%
-72.54%
Sales/Revenue/Turnover
- -
- -
- -
Total Cash Common Dividend
- -
- -
- -

Quarterly Revenue

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
1
- -
1
- -
2
2026
- -
- -
- -
- -
- -

Quarterly Earnings Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Quarterly Dividends Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -
Business
Humacyte, Inc. (Nasdaq: HUMA) develops and manufactures universally implantable, off-the-shelf, bioengineered human tissues and organs primarily for vascular repair, reconstruction, and replacement to treat injuries, diseases, and chronic conditions; its core products and investigational candidates include the FDA-approved Symvess (acellular tissue engineered vessel, or ATEV) for extremity vascular trauma repair, human acellular vessels targeting arteriovenous access for hemodialysis (Phase 3), peripheral artery disease, coronary artery bypass grafting, and pediatric heart surgery, as well as advanced organ systems such as BioVascular Pancreas for Type 1 diabetes and lung applications, plus advanced tissue constructs including urinary conduits, tracheal replacement, and esophageal replacement—all leveraging a proprietary bioengineering platform that decellularizes human tissues to enable host cell repopulation with reduced infection risk and no immunosuppression requirement. Founded in 2004 and headquartered in Durham, North Carolina, the company operates principally in the United States with a focus on regenerative medicine for trauma centers, dialysis patients, military facilities, and cardiovascular indications. Recent developments include U.S. FDA approval of Symvess in December 2024 enabling commercial shipments following batch release authorization, expansion of intellectual property with a new U.S. patent in September 2025 for bioengineered esophagus extending protection to 2041 across the U.S., Europe, Canada, and Australia alongside coverage for trachea and urinary conduits, achievement of primary endpoints in the V007 Phase 3 trial for dialysis AV access, interim cost reductions targeting $50 million in savings with Q3 2025 R&D expenses dropping to $17 million, and plans for sales force expansion plus a supplemental BLA for dialysis in late 2026.