ATEV

Peripheral Arterial Disease (PAD)

Phase 2/3Ongoing

Key Facts

Indication
Peripheral Arterial Disease (PAD)
Phase
Phase 2/3
Status
Ongoing
Company

About Humacyte

Humacyte's mission is to develop and commercialize universally implantable, off-the-shelf, regenerative human tissues to treat injury and disease. Its foundational achievement is the December 2024 FDA approval of Symvess™ (acellular tissue engineered vessel-tyod) for vascular trauma repair, marking its entry into the commercial market. The company's strategy leverages its scalable Human Acellular Vessel (HAV) platform, now commercialized as the Acellular Tissue Engineered Vessel (ATEV™), to expand into large adjacent markets like arteriovenous (AV) access for hemodialysis and peripheral arterial disease (PAD). With a deep pipeline across three technology platforms, Humacyte is positioned to address multi-billion dollar markets with its first-of-its-kind regenerative products.

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About Humacyte

Humacyte's mission is to develop and commercialize universally implantable, off-the-shelf, regenerative human tissues to treat injury and disease. Its foundational achievement is the December 2024 FDA approval of Symvess™ (acellular tissue engineered vessel-tyod) for vascular trauma repair, marking its entry into the commercial market. The company's strategy leverages its scalable Human Acellular Vessel (HAV) platform, now commercialized as the Acellular Tissue Engineered Vessel (ATEV™), to expand into large adjacent markets like arteriovenous (AV) access for hemodialysis and peripheral arterial disease (PAD). With a deep pipeline across three technology platforms, Humacyte is positioned to address multi-billion dollar markets with its first-of-its-kind regenerative products.

View full company profile

About Humacyte

Humacyte's mission is to develop and commercialize universally implantable, off-the-shelf, regenerative human tissues to treat injury and disease. Its foundational achievement is the December 2024 FDA approval of Symvess™ (acellular tissue engineered vessel-tyod) for vascular trauma repair, marking its entry into the commercial market. The company's strategy leverages its scalable Human Acellular Vessel (HAV) platform, now commercialized as the Acellular Tissue Engineered Vessel (ATEV™), to expand into large adjacent markets like arteriovenous (AV) access for hemodialysis and peripheral arterial disease (PAD). With a deep pipeline across three technology platforms, Humacyte is positioned to address multi-billion dollar markets with its first-of-its-kind regenerative products.

View full company profile

Other Peripheral Arterial Disease (PAD) Drugs

DrugCompanyPhase
Drug-Coated Balloon (DCB)ArteriusPre-clinical
ArterioSorb™ Bioresorbable ScaffoldArteriusPre-clinical
ETR-based GraftXeltisPre-clinical