<div id="readability-page-1"><div> By Kelly Cloonan <pre></pre> Humacyte's bioengineered human blood vessel met its primary endpoint for dialysis access in a recent Phase 3 trial. The commercial-stage biotechnology platform company's acellular tissue engineered vessel had an average of 91 more catheter-free days compared to autologous arteriovenous fistula, the current standard of care, in the first 80 patients enrolled in the study. The study will now end enrollment and continue to follow existing patients, in accordance with its protocol after meeting the primary endpoint, the company said Wednesday. Humacyte expects to file a supplemental biologic license application with the Food and Drug Administration in the second half. It currently plans to target an indication focused on adult patients with end-stage kidney disease who are at increased risk of AVfistula maturation failure, the company said. Separately, Humacyte also said it has commenced an underwritten public offering of its common stock. The number of shares it plans to sell wasn't disclosed. The company will grant the underwriters a 30-day option to purchase up to an additional 15% of the number of shares sold in the offering. Humacyte plans to use the proceeds from the offering to fund the commercialization of Symvess, for the planned filing of a BLA supplement in a hemodialysis indication and to develop product candidates in its pipeline. <pre></pre> Write to Kelly Cloonan at kelly.cloonan@wsj.com <pre></pre> (END) Dow Jones Newswires June 10, 2026 17:17 ET (21:17 GMT)Copyright (c) 2026 Dow Jones &amp; Company, Inc.</div></div>

HUMA

Humacyte 的生物工程血管在一項針對透析通路的三期臨牀試驗中達到了主要終點，顯示出比標準治療多出 91 天的無導管使用天數。該公司將在下半年結束招募並向 FDA 提交生物製品許可申請補充。此外，Humacyte 還啓動了一項承銷的普通股公開發行，以資助 Symvess 的商業化和管道開發

Humacyte 的生物工程血管在三期臨牀試驗中達到了主要終點