Lyell Immunopharma, Inc. (NASDAQ:LYEL – Get Free Report) Director Sumant Ramachandra bought 200,000 shares of the firm’s stock in a transaction that occurred on Friday, March 21st. The stock was acquired at an average cost of $0.58 per share, with a total value of $116,000.00. Following the transaction, the director now owns 200,000 shares of the company’s stock, valued at $116,000. This represents a ∞ increase in their position. The acquisition was disclosed in a legal filing with the SEC, which is accessible through this hyperlink.
Lyell Immunopharma Trading Down 6.1 %
Shares of NASDAQ:LYEL traded down $0.03 during trading on Tuesday, hitting $0.53. 440,470 shares of the company were exchanged, compared to its average volume of 1,045,818. The stock has a market cap of $155.05 million, a price-to-earnings ratio of -0.66 and a beta of -0.41. Lyell Immunopharma, Inc. has a fifty-two week low of $0.48 and a fifty-two week high of $3.15. The firm has a fifty day moving average price of $0.61 and a two-hundred day moving average price of $0.87.
Lyell Immunopharma (NASDAQ:LYEL – Get Free Report) last issued its earnings results on Wednesday, March 12th. The company reported ($0.72) earnings per share for the quarter, missing analysts’ consensus estimates of ($0.20) by ($0.52). The firm had revenue of $0.01 million for the quarter. Lyell Immunopharma had a negative return on equity of 34.64% and a negative net margin of 323,792.09%. As a group, research analysts predict that Lyell Immunopharma, Inc. will post -0.78 EPS for the current year.
Institutional Investors Weigh In On Lyell Immunopharma
Wall Street Analyst Weigh In
Separately, HC Wainwright restated a “neutral” rating and issued a $1.00 price objective on shares of Lyell Immunopharma in a report on Thursday, March 13th.
Get Our Latest Stock Report on LYEL
Lyell Immunopharma Company Profile
Lyell Immunopharma, Inc, a clinical-stage cell therapy company, develops T cell reprogramming technologies for patients with solid tumors. The company develops therapies using an ex vivo genetic reprogramming technologies, such as c Jun overexpression and NR4A3 gene knockout, to endow resistance to T cell exhaustion; and an ex vivo epigenetic reprogramming technologies, including Epi R to generate population of T cells with durable stemness, and Stim R, a proprietary synthetic cell mimetic.
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