Humacyte is proud to announce that the FDA has granted full approval for our Acellular Tissue Engineered Vessel, a first-in-class, universally implantable, bioengineered human vessel for extremity arterial trauma. This approval is a significant milestone in regenerative medicine, offering a new treatment option for patients with severe arterial injuries. Congratulations to our incredible team and partners who made this possible! Read our Press Release Here: https://xmrrwallet.com/cmx.plnkd.in/ehm-q6CX See the Prescribing Information, including Boxed Warning: https://xmrrwallet.com/cmx.pbit.ly/4dl5tuL #Humacyte #FDAApproval #RegenerativeMedicine #Innovation #Biotech #Firstinclass $HUMA
Humacyte
Biotechnology Research
Durham, NC 14,065 followers
Our vision is to be the global leader in engineering regenerative medicine products to save and improve patient lives.
About us
Humacyte, Inc. (Nasdaq: HUMA) is proud to announce that in Dec 2024, FDA granted full approval for our Acellular Tissue Engineered Vessel (ATEV), a first-in-class, universally implantable, bioengineered human vessel for extremity arterial trauma. This approval is a significant milestone in regenerative medicine, offering a new treatment option for patients with severe arterial injuries.See the Prescribing Information, including Boxed Warning: https://xmrrwallet.com/cmx.pbit.ly/4dl5tuL This is the first approval in our bioengineered ATEV Platform where we are continuing to investigate use of our lab-grown tissues and organs to improve the lives of patients and transform the practice of medicine. We develop and manufacture acellular tissues that are meant to be universally implantable and remodel with the patient's own cells over time. The goal is to grow spare parts for people. Humacyte’s ATEV is in clinical trials for arteriovenous access for hemodialysis, and peripheral arterial disease. Investigational 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 ATEV for performing hemodialysis in AV Access was the first indication to receive the FDA’s Regenerative Medicine Advanced Therapy (RMAT) expedited review designation, and the ATEV technology received priority designation for the treatment of extremity arterial repair by the U.S. Secretary of Defense prior to its FDA approval in Dec 2024 for that purpose. For more information, visit https://xmrrwallet.com/cmx.pHumacyte.com.
- Website
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https://xmrrwallet.com/cmx.phumacyte.com
External link for Humacyte
- Industry
- Biotechnology Research
- Company size
- 201-500 employees
- Headquarters
- Durham, NC
- Type
- Public Company
- Founded
- 2004
- Specialties
- Regenerative Medicine, biotechnology, and bioengineering
Locations
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Primary
2525 E NC Highway 54
2525 E Hwy 54
Durham, NC 27713, US
Employees at Humacyte
Updates
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Humacyte reposted this
The 2025 Military Health System Research Symposium (#MHSRS) kicks off today! We’re joining military medical researchers, innovators, and leaders from across the globe to share breakthroughs that advance the health and readiness of our warfighters. Stay tuned for updates on the future of military medicine—from battlefield trauma care to cutting-edge brain health research. #MilitaryHealth #WarfighterCare
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What a strong beginning to MHSRS 2025! Join us on Monday, August 4th for a session on ATEV™ at MHSRS. 🕔 Don’t miss Charles Fox, MD, LTC (Ret.), U.S. Army, presenting: “Real-World Implementation of a Bioengineered Vascular Conduit in Wartime Medicine: Lessons from Ukraine” 📅 Time: 1700 – 1715 (5:00–5:15 PM) EST 📍 Session ID: MHSRS-25-16832 This is the final talk in a 2-hour session running from 3:30–5:30 PM, followed by a 15-minute Q&A. About Dr. Fox: Director of Vascular Surgery, University of Maryland Capital Region Attending Surgeon at Shock Trauma & University of Maryland Medical Centers Associate Professor of Surgery, University of Maryland School of Medicine U.S. Army: LTC (Ret.), Combat Medic at 82nd Airborne Division Learn more about Humacyte’s Acellular Tissue Engineered Vessel (ATEV™) and ECAT approval visit us at Booth 1021 to connect with our clinical and sales teams. https://xmrrwallet.com/cmx.phumacyte.com Trademarks are property of Humacyte Global, Inc © 2025 Humacyte Global Inc. All Rights Reserved. #Humacyte #Innovation #Biotech #MHSRS2025 #MHSRS #MTEC #MilitaryMedicine #ECATapproved #DefenseHealth $HUMA
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Stop by booth 1021 during the MHSRS conference from August 4th – 7th. With our recent ECAT (Electronic Catalog) listing you can find our product in the DLA (Defense Logistics Agency) medical supply chain procurement system. The Humacyte team is ready to let you handle and help you learn more about our FDA Approved Symvess™, a first-in-class, universally implantable, bioengineered human vessel for extremity vascular trauma replacement and repair. Our sales and medical affairs teams will be there to answer all your questions. Learn more about Symvess here: https://xmrrwallet.com/cmx.plnkd.in/e2jnB-eg SEE FULL PRESCRIBING INFORMATION INCLUDING BOXED WARNING AND IMPORTANT SAFETY INFORMATION at https://xmrrwallet.com/cmx.pbit.ly/4dl5tuL INDICATION SYMVESS is an acellular tissue engineered vessel indicated for use in adults as a vascular conduit for extremity arterial injury when urgent revascularization is needed to avoid imminent limb loss, and autologous vein graft is not feasible. GRAFT FAILURE: loss of SYMVESS integrity due to mid-graft rupture or anastomotic failure can result in life threatening hemorrhage. DO NOT use SYMVESS in patients who have a medical condition that would preclude long-term antiplatelet therapy after acute injury resolution. WARNINGS AND PRECAUTIONS: Vascular Graft Rupture, Anastomotic Failure, and Thrombosis have occurred in patients treated with SYMVESS. SYMVESS is manufactured using cells and reagents that may transmit infectious diseases or agents; none have been reported during clinical testing. ADVERSE REACTIONS: most common (≥3%): thrombosis, fever, pain, anastomotic stenosis, rupture or anastomotic failure, and infection. Trademarks are property of Humacyte Global, Inc © 2025 Humacyte Global Inc. All Rights Reserved. US-SYM-000262 @affirmative-solutions Apiary Medical Inc. #Humacyte #Innovation #Biotech #MHSRS2025 #MHSRS #MTEC #MilitaryMedicine #ECATapproved #DefenseHealth $HUMA
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Humacyte reposted this
Exciting news coming from MTEC member, Humacyte! Congratulations!! Learn more about MTEC projects that Humacyte has worked on in their member profile: https://xmrrwallet.com/cmx.plnkd.in/gX4usnR5 #MTECmember #medtech #innovation #FDAapproved FDA
Humacyte is proud to announce that the FDA has granted full approval for our Acellular Tissue Engineered Vessel, a first-in-class, universally implantable, bioengineered human vessel for extremity arterial trauma. This approval is a significant milestone in regenerative medicine, offering a new treatment option for patients with severe arterial injuries. Congratulations to our incredible team and partners who made this possible! Read our Press Release Here: https://xmrrwallet.com/cmx.plnkd.in/ehm-q6CX See the Prescribing Information, including Boxed Warning: https://xmrrwallet.com/cmx.pbit.ly/4dl5tuL #Humacyte #FDAApproval #RegenerativeMedicine #Innovation #Biotech #Firstinclass $HUMA
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Major Milestone in Biotech Options for the U.S. Military Humacyte has officially made its first sale of Symvess™, a bioengineered human vessel, to a U.S. Military Treatment Facility—marking a breakthrough in patient care for service members and veterans. Following FDA approval and ECAT listing, Symvess is now available across 35 military hospitals and 160 VA facilities. This is more than a sale - it's a step toward transforming how we treat vascular trauma. Read the full press release here: https://xmrrwallet.com/cmx.plnkd.in/earTginP Trademarks are property of Humacyte Global, Inc © 2025 Humacyte Global Inc. All Rights Reserved. #Biotech #RegenerativeMedicine #MilitaryHealth #Humacyte #Symvess #FDAApproved #InnovationInCare #VeteransHealth #HealthcareBreakthrough
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Humacyte reposted this
SAVING LIVES IN UKRAINE- A VASCULAR SURGEON'S STORY Great to speak with Ukrainian Vascular Surgeon, Dr. Oleksandr Sokolov, about his incredible experiences treating severely war-wounded patients in an active combat zone in Ukraine. He described his use of Acellular Tissue Engineered Vessels for vascular reconstruction following combat trauma and the advantages compared to other modalities, such as autologous vein and PTFE or Gore-Tex. He explains how this technology can improve patient outcomes even in the most austere environments. Keep an eye out for an updated series from his team in Military Medicine, the AMSUS - The Society of Federal Health Professionals journal. We are also looking forward to putting out this video and podcast episode on WarDocs soon. Excelsior Surgical Society American College of Surgeons Society for Vascular Surgery European Society for Vascular Surgery Humacyte Joint Trauma System (JTS) DoD Center of Excellence for Trauma Oxford University Press
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Humacyte has just announced that Symvess™ has been awarded Electronic Catalog (ECAT) listing approval from the U.S. Defense Logistics Agency, which makes Symvess available to healthcare professionals at U.S. Department of Defense and U.S. Department of Veterans Affairs facilities. For more details, please read the full press release here: https://xmrrwallet.com/cmx.plnkd.in/eQK3PVJY #Humacyte #HealthcareInnovation #Bioengineering #Biotech
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Humacyte reposted this
In a trial, an acellular tissue engineered vessel had superior functional patency for hemodialysis with acceptable safety compared with an arteriovenous fistula in high-risk patients. https://xmrrwallet.com/cmx.plnkd.in/eZ3BK_Kq #dialysis