Lyell Immunopharma, Inc. (NASDAQ:LYEL – Get Free Report) saw a large increase in short interest in June. As of June 15th, there was short interest totalling 24,150,000 shares, an increase of 19.6% from the May 31st total of 20,200,000 shares. Based on an average trading volume of 788,600 shares, the short-interest ratio is presently 30.6 days. Approximately 20.4% of the shares of the stock are short sold.
Lyell Immunopharma Stock Down 4.4 %
Shares of Lyell Immunopharma stock traded down $0.07 during mid-day trading on Tuesday, hitting $1.51. The stock had a trading volume of 934,752 shares, compared to its average volume of 1,033,032. The firm has a 50-day moving average of $2.38 and a two-hundred day moving average of $2.24. Lyell Immunopharma has a 12-month low of $1.18 and a 12-month high of $3.41. The firm has a market cap of $384.96 million, a P/E ratio of -1.68 and a beta of -0.52.
Lyell Immunopharma (NASDAQ:LYEL – Get Free Report) last posted its quarterly earnings results on Monday, May 6th. The company reported ($0.24) earnings per share for the quarter, missing the consensus estimate of ($0.20) by ($0.04). Lyell Immunopharma had a negative net margin of 335,794.09% and a negative return on equity of 33.92%. Sell-side analysts expect that Lyell Immunopharma will post -0.85 earnings per share for the current year.
Institutional Trading of Lyell Immunopharma
Analysts Set New Price Targets
Several brokerages recently issued reports on LYEL. Bank of America dropped their price objective on shares of Lyell Immunopharma from $9.00 to $6.00 and set a “buy” rating for the company in a research note on Thursday, June 27th. HC Wainwright reaffirmed a “neutral” rating and set a $1.00 price objective (down previously from $6.00) on shares of Lyell Immunopharma in a research note on Thursday, June 27th.
Read Our Latest Stock Analysis on LYEL
About Lyell Immunopharma
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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