Lyell Immunopharma, Inc. (NASDAQ:LYEL – Get Free Report) CFO Charles W. Newton bought 200,000 shares of Lyell Immunopharma stock in a transaction dated 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 completion of the acquisition, the chief financial officer now directly owns 200,000 shares in the company, valued at $112,000. This represents a ∞ increase in their ownership of the stock. The purchase was disclosed in a document filed with the Securities & Exchange Commission, which is available through this link.
Lyell Immunopharma Price Performance
Shares of LYEL traded down $0.03 on Tuesday, hitting $0.48. The company’s stock had a trading volume of 1,199,720 shares, compared to its average volume of 1,043,773. The company has a market capitalization of $142.80 million, a PE ratio of -0.61 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 company has a 50 day moving average price of $0.62 and a 200 day moving average price of $0.90.
Lyell Immunopharma (NASDAQ:LYEL – Get Free Report) last announced its earnings results on Wednesday, March 12th. The company reported ($0.72) EPS for the quarter, missing the consensus estimate of ($0.20) by ($0.52). The business had revenue of $0.01 million during the quarter. Lyell Immunopharma had a negative return on equity of 34.64% and a negative net margin of 323,792.09%. On average, equities analysts forecast that Lyell Immunopharma, Inc. will post -0.78 EPS for the current year.
Institutional Inflows and Outflows
Wall Street Analysts Forecast Growth
Separately, HC Wainwright reissued a “neutral” rating and issued a $1.00 target price on shares of Lyell Immunopharma in a report on Thursday, March 13th.
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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