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Humacyte to Present at the Piper Sandler 36th Annual Healthcare Conference

Key Takeaway: Humacyte, Inc. will participate in the Piper Sandler 36th Annual Healthcare Conference on December 5, 2024, where CEO Laura Niklason will present. The company is advancing its bioengineered human tissue platform, with products in late-stage clinical trials for various vascular applications. A Biologics License Application for one of its candidates is currently under FDA review. The firm has received multiple FDA designations for its innovative products.

Market Sentiment Analysis

POSITIVE FACTORS

  • Humacyte is at the forefront of developing bioengineered human tissues.
  • The company has received Priority Review from the FDA for its product candidates.
  • Management will engage with investors at a prestigious healthcare conference.

Full Press Release Details

DURHAM, N.C., Dec. 02, 2024 (GLOBE NEWSWIRE) -- Humacyte, Inc. (Nasdaq: HUMA), a clinical-stage biotechnology platform company developing universally implantable, bioengineered human tissue at commercial scale, today announced that Laura Niklason, M.D., Ph.D., Founder, President, and Chief Executive Officer, will participate in a fireside chat presentation at the Piper Sandler 36th Annual Healthcare Conference, in New York, NY on Thursday, December 5, 2024. Management will also be available for one-on-one meetings.
Event: Piper Sandler 36th Annual Healthcare Conference
Location: The Lotte New York Palace, NY
Presentation: Thursday, December 5, 8:00 a.m. EST
A replay will be available for a limited time following the presentation on the Events & Presentations portion of the Humacyte website.
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. Humacyte develops and manufactures acellular tissues to treat a wide range of diseases, injuries, and chronic conditions. Humacyte’s initial product candidates, a portfolio of ATEVs, are currently in late-stage clinical trials targeting multiple vascular applications, including vascular trauma repair, arteriovenous (AV) access for hemodialysis, and peripheral artery disease. A Biologics License Application for the ATEV in the vascular trauma indication is currently under review by the FDA and was granted Priority Review. 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 an 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:
LifeSci Advisors LLC
Humacyte Media Contact:
Precision Strategies

Frequently Asked Questions

When is the fireside chat with Laura Niklason?

The fireside chat is scheduled for December 5, 2024, at 8:00 a.m. EST.

Where is the Piper Sandler Healthcare Conference held?

The conference will take place at The Lotte New York Palace, NY.

What is Humacyte's focus in biotechnology?

Humacyte focuses on developing universally implantable bioengineered human tissues.

What designations has Humacyte's ATEV received?

Humacyte's ATEV has received RMAT and Fast Track designations from the FDA.

How can I watch the presentation after it airs?

A replay will be available on Humacyte's website after the presentation.

Last updated: Dec 2, 2024