Humacyte, Inc. (NASDAQ:HUMA – Get Free Report) has been assigned a consensus recommendation of “Moderate Buy” from the eight brokerages that are covering the company, MarketBeat Ratings reports. One investment analyst has rated the stock with a sell rating and seven have given a buy rating to the company. The average 12 month price target among brokers that have covered the stock in the last year is $8.1429.
HUMA has been the topic of several analyst reports. D. Boral Capital reaffirmed a “buy” rating and set a $25.00 target price on shares of Humacyte in a research report on Thursday. HC Wainwright reiterated a “buy” rating and issued a $3.00 target price on shares of Humacyte in a research note on Monday, December 1st. BTIG Research reiterated a “buy” rating and issued a $6.00 target price on shares of Humacyte in a report on Monday, February 9th. Wall Street Zen cut shares of Humacyte from a “hold” rating to a “sell” rating in a report on Sunday, December 21st. Finally, Weiss Ratings reiterated a “sell (d-)” rating on shares of Humacyte in a research note on Monday, December 29th.
Check Out Our Latest Research Report on HUMA
Institutional Investors Weigh In On Humacyte
Humacyte Trading Up 6.5%
NASDAQ:HUMA opened at $1.15 on Tuesday. The company has a debt-to-equity ratio of 2.97, a current ratio of 1.62 and a quick ratio of 0.90. Humacyte has a one year low of $0.88 and a one year high of $3.94. The company has a market cap of $215.36 million, a PE ratio of -5.00 and a beta of 1.93. The firm has a 50-day moving average of $1.07 and a 200-day moving average of $1.41.
About Humacyte
Humacyte, Inc is a clinical-stage biotechnology company focused on the development and manufacturing of off-the-shelf, regenerative human acellular vessels (HAVs) designed to address critical vascular access needs. The company’s proprietary vessels are engineered from human donor cells and then decellularized to create a biocompatible scaffold capable of integrating with a patient’s own tissue. Humacyte’s primary business activities encompass process development, large-scale manufacturing, and clinical evaluation of HAVs for use in end-stage renal disease, peripheral arterial disease and other vascular repair applications.
The company’s lead product candidate, the HAV, has advanced through multiple clinical trials for arteriovenous access in hemodialysis patients, demonstrating durability, reduced infection rates and compatibility with repeated cannulation.
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