Humacyte
Manufacturing · North Carolina, United States · 51-200 Employees
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Overview
Headquarters
2525 E North Carolina Hwy 54, Durham, No...Phone Number
(919) 313-9633Website
www.humacyte.comRevenue
<$5 MillionStock Symbol
HUMAIndustry
ZI Rank: 1
Signal Type
Jan
Feb
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Jun
ZI Rank
3
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1
About Humacyte
Humacyte, Inc. engages in the development and manufacture of off-the-shelf, implantable, and bioengineered human tissues for the treatment of diseases and conditions across a range of anatomic locations in multiple therapeutic areas. The company using its proprietary and scientific technology platform to engineer and manufacture human acellular vessels (HAVs) to be implanted into patient without inducing a foreign body response or leading to immune rejection. It is developing a portfolio of HAVs, which would target the vascular repair, reconstruction, and replacement market, including vascular trauma; arteriovenous access for hemodialysis; peripheral arterial disease; pediatric heart surgery; and coronary artery bypass grafting, as well as for the delivery of cellular therapy, including pancreatic islet cell transplantation to treat Type 1 diabetes. The company was founded in 2004 and is headquartered in Durham, North Carolina.Explore more
Humacyte Org Chart
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Activity Insights
Humacyte is experiencing very low activity levels compared to other companies in the Manufacturing sector.
What does this means?
Humacyte is drawing exceptional interest within the Manufacturing industry, suggesting notable developments or strong market momentum, learn more about Humacyte.
Humacyte financials insights
Gather financial insights about Humacyte, including details on funding rounds, investors, total funding, and acquisitions, to gain a comprehensive understanding of their financial strategy.
2015
Series B
$150M
2016
Private Equity
$10M
2017
Unspecified
$14.1M
2018
Other Financing Round
$150M
2020
Debt
$2M
2021
Debt
$50M
2023
Debt
$150M
Humacyte Tech Stack
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Open Position
Open Position
Partnership
Project
Laboratory Operations, Medical Research, Clinical Operations
Project
reported a favorable safety profile for the ATEV in the V012 trial, with total adverse events of 235 in the ATEV arm versus 287 in the AVF arm (rates of 8.9 versus 18 per patient-year), serious adverse events of 46 versus 75 (rates of 1.73 versus 4.77), and zero access-related infections in the ATEV arm compared to 3 in the AVF arm. No new or unexpected safety concerns were identified, and no study access ruptures occurred in either arm.
Project
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Frequently Asked Questions Regarding Humacyte
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Humacyte, Inc. engages in the development and manufacture of off-the-shelf, implantable, and bioengineered human tissues for the treatment of diseases and conditions across a range of anatomic locations in multiple therapeutic areas. The company using its proprietary and scientific technology platform to engineer and manufacture human acellular ves... Read More
