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Intellectia

HUMA News

Eligibility Verification for Huma Open Season 3 Airdrop

Feb 25 2026moomoo

Humacyte Secures Congressional Funding for Bioengineered Vessels

Feb 09 2026seekingalpha

Humacyte Secures DOD Funding for Bioengineered Blood Vessels

Feb 09 2026stocktwits

BTIG Affirms Buy Rating on Humacyte, Keeps $6 Price Target Intact

Nov 21 2025Benzinga

D. Boral Capital Reiterates Buy Rating on Humacyte with $25 Price Target Intact

Nov 20 2025Benzinga

Benchmark Reaffirms Buy Rating on Humacyte, Adjusts Price Target to $11

Nov 13 2025Benzinga

D. Boral Capital Reiterates Buy Rating on Humacyte with $25 Price Target Intact

Nov 12 2025Benzinga

Robust Earnings and Biotech Strength Drive Midweek Momentum

Nov 12 2025Newsfilter

HUMA Events

02/20 08:50
Liquid Option Borrow Rates Increase
Latest data shows the largest indicative borrow rate increases among liquid option names include: Sellas Life Sciences (SLS) 20.00% +1.62, MSOX ETF (MSOX) 14.83% +0.65, Humacyte (HUMA) 20.83% +0.62, Velo3D Inc (VELO) 11.75% +0.59, ProShares Ultra VIX Short Term Futures (UVXY) 6.69% +0.54, Americas Silver (USAS) 1.02% +0.52, Draganfly (DPRO) 13.60% +0.42, Palladyne AI Corp (PDYN) 23.10% +0.40, Teucrium 2x Long Daily XRP ETF (XXRP) 3.31% +0.31, and Sidus Space Inc (SIDU) 11.40% +0.31.
02/18 08:30
Humacyte Presents Long-Term Data on Symvess at VESS Annual Meeting
Humacyte announced the presentation of long-term data assessing the durability of Symvess in extremity arterial trauma patients at the Annual Winter Meeting 2026 for the Vascular & Endovascular Surgery Society, VESS, in Olympic Valley, CA. The presentation, titled "Long-Term Outcomes of the Acellular Tissue Engineered Vessel in Extremity Arterial Trauma Repair: Results from the V005 Trial." In the V005 trial, Symvess maintained long-term structural integrity, exhibited low infection rates, and supported high rates of limb salvage in patients who were followed for up to 36 months. Among those treated in the V005 Phase 2/3 study were 54 patients who underwent extremity vascular repair with Symvess for whom treatment with autologous vein, the standard of care, was not feasible. Within this patient population, once early complications from the traumatic injuries resolved, the rates of conduit infection, limb salvage, and patient survival plateaued and remained relatively constant through the three years of follow-up. Symvess maintained an infection-free rate of 92.9% from months 3-36, with no infections after day 37 and only three conduit infections overall. Limb salvage rates were 87.3% at 12 months and 82.5% at 24 months, despite a severely injured trauma cohort.
02/09 08:30
Humacyte Secures Funding for Biologic Vascular Repair Technologies from DoD
Humacyte announced that the recently adopted FY 2026 U.S. Department of Defense Appropriations Act includes dedicated funding to support the evaluation and incorporation of biologic vascular repair technologies for the warfighters suffering from traumatic vascular injuries. The FY2026 National Defense Authorization Act, enacted in December 2025, stated in report language that DoD should "integrate FDA-approved breakthrough vascular repair technologies in traumatic extremity arterial injury repair, providing an off-the-shelf, biologically active vascular conduit when autologous vein harvesting is not feasible." Humacyte said: "In doing so, lawmakers demonstrated that they recognize and understand the need for human-derived bioengineered vessels to save life and limb on the battlefield. Humacyte is grateful to see Congress express even greater support for this medical innovation by designating appropriated funds to advance the goal of making this groundbreaking technology available to service members."

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