Hyperion DeFi, Inc. (NASDAQ:HYPD – Get Free Report) Director Ellen Strahlman acquired 3,601 shares of the business’s stock in a transaction that occurred on Friday, December 26th. The shares were purchased at an average cost of $3.86 per share, for a total transaction of $13,899.86. Following the acquisition, the director owned 79,049 shares in the company, valued at $305,129.14. This represents a 4.77% increase in their ownership of the stock. The acquisition was disclosed in a legal filing with the Securities & Exchange Commission, which is available through this link.
Hyperion DeFi Price Performance
HYPD traded down $0.13 on Tuesday, reaching $3.37. The stock had a trading volume of 193,370 shares, compared to its average volume of 1,525,525. The company has a current ratio of 2.25, a quick ratio of 2.25 and a debt-to-equity ratio of 0.11. The company has a market capitalization of $27.53 million, a price-to-earnings ratio of -0.83 and a beta of 2.81. Hyperion DeFi, Inc. has a fifty-two week low of $0.85 and a fifty-two week high of $17.99. The firm has a 50-day moving average of $4.87 and a 200-day moving average of $7.60.
Hyperion DeFi (NASDAQ:HYPD – Get Free Report) last announced its quarterly earnings results on Friday, November 14th. The company reported $0.05 EPS for the quarter. The firm had revenue of $0.36 million for the quarter. Hyperion DeFi had a negative return on equity of 119.59% and a negative net margin of 62,238.41%. As a group, sell-side analysts anticipate that Hyperion DeFi, Inc. will post -41.6 EPS for the current year.
Wall Street Analysts Forecast Growth
View Our Latest Stock Report on HYPD
About Hyperion DeFi
Eyenovia, Inc, an ophthalmic technology company, engages in the development of therapeutics based on its proprietary microdose array print platform technology. The company's product candidates include MicroPine, which is in Phase III clinical development program with indications for pediatric myopia progression (near-sightedness); MicroLine, which is in Phase III clinical development program with indications for the improvement in near vision in people with presbyopia; and Mydcombi, which is in Phase III clinical development program with indications for pharmaceutical mydriasis.
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