Lyell Immunopharma, Inc. (NASDAQ:LYEL – Get Free Report) CFO Charles W. Newton acquired 200,000 shares of Lyell Immunopharma stock in a transaction that occurred on Monday, March 17th. The stock was acquired at an average cost of $0.56 per share, for a total transaction of $112,000.00. Following the purchase, the chief financial officer now owns 200,000 shares of the company’s stock, valued at $112,000. The trade was a ∞ increase in their ownership of the stock. The acquisition was disclosed in a document filed with the Securities & Exchange Commission, which is available through this link.
Lyell Immunopharma Stock Performance
Lyell Immunopharma stock opened at $0.53 on Friday. The firm has a 50 day moving average price of $0.61 and a two-hundred day moving average price of $0.89. Lyell Immunopharma, Inc. has a 52-week low of $0.48 and a 52-week high of $3.15. The firm has a market cap of $157.45 million, a price-to-earnings ratio of -0.68 and a beta of -0.41.
Lyell Immunopharma (NASDAQ:LYEL – Get Free Report) last announced 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). Lyell Immunopharma had a negative return on equity of 34.64% and a negative net margin of 323,792.09%. The firm had revenue of $0.01 million for the quarter. As a group, equities research analysts predict that Lyell Immunopharma, Inc. will post -0.78 EPS for the current fiscal year.
Institutional Investors Weigh In On Lyell Immunopharma
Analysts Set New Price Targets
Separately, HC Wainwright reiterated a “neutral” rating and issued a $1.00 price target on shares of Lyell Immunopharma in a research report on Thursday, March 13th.
Get Our Latest Stock Analysis on Lyell Immunopharma
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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