HUMAWHIGH SIGNALOPERATIONAL10-K

Humacyte achieved commercial launch of its Symvess product for vascular trauma while substantially improving its financial position through meaningfully reduced losses and lower liabilities.

The language changes indicate Humacyte has successfully transitioned from a pure clinical-stage company to commercial operations, with Symvess now available for vascular trauma patients beyond clinical trials. The company expanded its outstanding shares by approximately 43% (from 155M to 222M shares), suggesting recent capital raising activities that have strengthened the balance sheet and funded the commercial launch.

Comparing 2026-03-27 vs 2025-03-31View on EDGAR →
FINANCIAL ANALYSIS

Humacyte demonstrated substantial financial improvement with net losses meaningfully reduced while maintaining strong cash reserves that grew modestly to $50.5M. The company decreased R&D spending by over 20% and cut total liabilities significantly from $190.5M to $113.3M, indicating improved financial discipline coinciding with the transition to commercial operations. Current assets expanded notably to $67.8M, providing enhanced liquidity to support the commercial launch phase.

FINANCIAL STATEMENT CHANGES
Net Income
P&L
+72.5%
-$148.7M-$40.8M

Net income grew 72.5% — bottom-line growth signals improving overall business health.

Capital Expenditure
Cash Flow
-43.8%
$1.6M$884K

Capex reduced 43.8% — investment cycle winding down or capital discipline; may improve near-term free cash flow.

Current Assets
Balance Sheet
+41.7%
$47.9M$67.8M

Current assets grew 41.7% — improving short-term liquidity or inventory/receivables build.

Total Liabilities
Balance Sheet
-40.6%
$190.5M$113.3M

Liabilities reduced 40.6% — deleveraging improves balance sheet strength and financial flexibility.

R&D Expense
P&L
-21.8%
$88.6M$69.3M

R&D spending cut 21.8% — could signal cost discipline or concerning reduction in innovation investment.

Total Assets
Balance Sheet
-15.6%
$137.9M$116.4M

Total assets contracted 15.6% — asset sales, write-downs, or balance sheet optimization underway.

Cash & Equivalents
Balance Sheet
+12.4%
$44.9M$50.5M

Cash grew 12.4% — improving liquidity position supports investment and shareholder returns.

LANGUAGE CHANGES
NEW — 2026-03-27
PRIOR — 2025-03-31
ADDED
As of March 24, 2026, 222,019,108 shares of common stock, par value $0.0001, were issued and outstanding.
We are initially using our proprietary, scientific technology platform to engineer and manufacture acellular tissue engineered vessels, or ATEVs.
As of December 31, 2025, our ATEVs have been implanted in approximately 636 patients in clinical trials as well as additional patients following the U.S.
commercial launch of Symvess in the vascular trauma indication.
In addition to vascular trauma, we are currently conducting a Phase 3 trial of our 6 millimeter ATEV in AV access for hemodialysis, and previously completed Phase 2 trials in PAD.
AV Access for Hemodialysis : An estimated $5 to $6 billion per year is spent on hospital admissions in hemodialysis patients with infection and access complications.
In Europe and Asia, the number of patients suffering with Type 1 diabetes is estimated at approximately 2.8 million and 2.0 million, respectively.
Typically, a CABG operation involves the use of both the patient s own artery and vein.
There are approximately 1,800 babies born in the United States with Tetralogy of Fallot each year.
Primary analysis based on a total of 51 patients with injuries of extremities BLA approved by FDA December 19, 2024 30-day PP: 84.3% 30-day SP: 90.2% Infection Rate: 2.0% Amputation Rate: 9.8% V017 Vascular Trauma 2022 Retrospective observational study to evaluate the ATEV in real-world setting of humanitarian program conducted during wartime in Ukraine 19 total treated under humanitarian program.
REMOVED
As of March 27, 2025, 155,118,816 shares of common stock, par value $0.0001, were issued and outstanding.
We are initially using our proprietary, scientific technology platform to engineer and manufacture acellular tissue engineered vessels, or ATEVs TM .
As of December 31, 2024, our ATEVs have been implanted in approximately 601 patients.
In addition to vascular trauma, we and our collaborators are currently conducting Phase 3 and Phase 2 trials of our 6 millimeter ATEV in AV access for hemodialysis and PAD.
In addition, in 2018 our ATEV product candidate was assigned a priority designation by the Secretary of Defense under Public Law 115-92, enacted to expedite the FDA s review of products that are intended to diagnose, treat or prevent serious or life-threatening conditions facing American military personnel.
In September 2023, we announced positive topline results from our V005 Phase 2/3 trial in vascular trauma, and in December 2023 we filed a Biologics License Application ( BLA ) for urgent arterial repair following extremity vascular trauma when synthetic graft is not indicated, and autologous vein use is not feasible.
On August 9, 2024, the FDA informed us that it required additional time to complete its review of the BLA for the vascular trauma indication.
( Legacy Humacyte ), a Delaware corporation, and Alpha Healthcare Acquisition Corp.
In addition, the Budget Impact Model for the ATEV, published in the Journal of Medical Economics in March 2025, reported that the ATEV was projected to be cost saving for both trauma centers and third-party payors, primarily due to reductions in the costs related to amputations and conduit infections.
In the EU4 (France, Germany, Italy and Spain) and the UK, the number of patients suffering with Type 1 diabetes is estimated at approximately 1.5 million.
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