Humacyte Announces Date of Annual Shareholder Meeting
Humacyte, Inc. (Nasdaq: HUMA) will hold its 2022 annual meeting of shareholders virtually on June 9, 2022, at 7:30 AM ET. The record date for eligible voters is April 18, 2022. Humacyte is focused on developing a platform for universally implantable bioengineered human tissues, with an emphasis on human acellular vessels (HAVs). These vessels are in late-stage clinical trials for vascular applications, receiving FDA's Regenerative Medicine Advanced Therapy designation, and are prioritized for vascular trauma by the U.S. Secretary of Defense.
- Humacyte's HAVs are in late-stage clinical trials for multiple applications, indicating strong progress in product development.
- The 6mm HAV received FDA's Regenerative Medicine Advanced Therapy designation, suggesting accelerated review and approval potential.
- Humacyte's technology has been prioritized for treatment of vascular trauma by the U.S. Secretary of Defense, highlighting its significance.
- None.
DURHAM, N.C., April 04, 2022 (GLOBE NEWSWIRE) -- Humacyte, Inc. (Nasdaq: HUMA), a clinical-stage biotechnology platform company developing universally implantable bioengineered human tissue at commercial scale, today announced that its 2022 annual meeting of shareholders will be held virtually on Thursday, June 9, 2022, at 7:30 AM eastern time.
The record date for those eligible to receive notice of and to vote at the annual meeting is Monday, April 18, 2022.
About Humacyte
Humacyte, Inc. (Nasdaq: HUMA) is developing a disruptive biotechnology platform to deliver universally implantable bioengineered human tissues and organs 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 initial opportunity, a portfolio of human acellular vessels (HAVs), is currently in late-stage clinical trials targeting multiple vascular applications, including vascular trauma repair, arteriovenous access for hemodialysis, and peripheral arterial disease. 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 HAV for arteriovenous (AV) access for performing hemodialysis was the first product candidate to receive the FDA’s Regenerative Medicine Advanced Therapy (RMAT) designation, and the HAV technology 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
jallaire@lifesciadvisors.com
investors@humacyte.com
Humacyte Media Contact:
Heather Anderson
6 Degrees
919-827-5539
handerson@6degreespr.com
media@humacyte.com
