Humacyte, INC 10-K annual reports

Annual reports — audited financials, the full risk-factor list, and management’s account of the year.

NASDAQ
Humacyte, Inc. commenced U.S. commercial sales of its FDA-approved Symvess for vascular trauma in Q1 2025, generating $1.4 million in revenue, but faces substantial doubt about its ability to continue as a going concern.
NASDAQ
Humacyte, Inc. announced FDA approval for its bioengineered tissue product Symvess for extremity vascular trauma and initiated its U.S. commercial launch in Q1 2025, while continuing Phase 3 trials for other indications and securing significant financing.
NASDAQ
Humacyte's 10-K filing provides a detailed description of its capital stock, including common and preferred shares, as well as the terms of outstanding warrants.