Press Releases September 10, 2026 08:00 AM

Humacyte to Present at the H.C. Wainwright 28th Annual Global Investment Conference

Humacyte to feature in high-profile investment conference, highlighting advanced regenerative medicine developments

By Marcus Reed
Share
Twitter Reddit Facebook LinkedIn
HUMA

Humacyte, a Nasdaq-listed biotechnology company specializing in bioengineered human tissues, announced participation in the H.C. Wainwright 28th Annual Global Investment Conference. The presentation will showcase its FDA-approved acellular tissue engineered vessel (ATEV) technology and ongoing clinical trials targeting vascular and other medical applications, reflecting significant progress in regenerative medicine.

Humacyte to Present at the H.C. Wainwright 28th Annual Global Investment Conference
HUMA
Summarize with
ChatGPT Perplexity Claude Grok Gemini

Key Points

  • Humacyte's ATEV received FDA approval in 2024 and multiple RMAT and Fast Track designations, underlining strong regulatory support.
  • The company is advancing late-stage clinical trials for vascular trauma, hemodialysis access, and peripheral artery disease applications, signaling a promising product pipeline.
  • Participation in a major investor conference increases visibility among investors and stakeholders, potentially boosting capital and partnerships.
  • Sectors impacted include biotechnology, healthcare, medical devices, and regenerative medicine markets.

DURHAM, N.C., Sept. 10, 2026 (GLOBE NEWSWIRE) -- Humacyte, Inc. (Nasdaq: HUMA), a commercial-stage biotechnology platform company developing universally implantable, bioengineered human tissues at commercial scale, today announced that Laura Niklason, M.D., Ph.D., Founder, President, and Chief Executive Officer, will participate in a fireside chat at the H.C. Wainwright 28th Annual Global Investment Conference in New York, NY on September 16, 2026, at 11:00am Eastern Time. Management will also be available for one-on-one meetings.

Event: H.C. Wainwright 28th Annual Global Investment Conference
Location: Lotte New York Palace Hotel, New York, NY
Presentation: Wednesday, September 16, 2026 at 11:00am ET
Webcast: click here

A replay will be available for a limited time following the presentation on the Events & Presentations portion of the Humacyte website.

About Humacyte

Humacyte, Inc. (Nasdaq: HUMA) is developing a disruptive biotechnology platform to deliver universally implantable bioengineered human tissues, advanced tissue constructs, and organ systems designed to improve the lives of patients and transform the practice of medicine. The Company develops and manufactures acellular tissues to treat a wide range of diseases, injuries, and chronic conditions. Humacyte’s Biologics License Application for the acellular tissue engineered vessel (ATEV) in the vascular trauma indication was approved by the FDA in December 2024. ATEVs are also currently in late-stage clinical trials targeting other vascular applications, including arteriovenous (AV) access for hemodialysis and peripheral artery disease (PAD). Preclinical development is also underway in coronary artery bypass grafts, pediatric heart surgery, treatment of type 1 diabetes, and multiple novel cell and tissue applications. Humacyte’s 6mm ATEV for AV access in hemodialysis was the first product candidate to receive the FDA’s Regenerative Medicine Advanced Therapy (RMAT) designation and has also received FDA Fast Track designation. Humacyte’s 6mm ATEV for urgent arterial repair following extremity vascular trauma and for advanced PAD also have received RMAT designations. The ATEV received priority designation for the treatment of vascular trauma by the U.S. Secretary of Defense. For more information, visit www.Humacyte.com.

Humacyte Investor Contact:
Joyce Allaire
LifeSci Advisors LLC
+1-617-435-6602
[email protected]
[email protected]

Humacyte Media Contact:
Rich Luchette
Precision Strategies
+1-202-845-3924
[email protected]
[email protected]


Risks

  • Clinical trial outcomes for ATEVs in different vascular and organ system applications remain uncertain, posing development risks.
  • Regulatory approvals beyond existing FDA designations are required for broader market adoption, introducing potential regulatory risks.
  • Commercial adoption challenges and competition in advanced tissue engineering and regenerative therapies may impact future revenue growth.

More from Press Releases

WidePoint to Present at the H.C. Wainwright 28th Annual Global Investment Conference on Tuesday, September 15, 2026, at 2:30pmET Sep 10, 2026 Precision Optics Announces Receipt of $1.3 Million Follow-On Production Orders from Large Defense Company Sep 10, 2026 RYET Signs MOU with Changan Anyi and Intersect for Saudi NEV Institute Sep 10, 2026 Omada Health to Present Updated Long-Term Financial Targets at Inaugural Investor Day Sep 10, 2026 Lite Strategy to Present at the 28th Annual H.C. Wainwright Global Investment Conference in New York Sep 10, 2026