Shares of Kyverna Therapeutics, Inc. (NASDAQ:KYTX – Get Free Report) have been assigned an average recommendation of “Buy” from the seven research firms that are currently covering the firm, Marketbeat.com reports. One analyst has rated the stock with a hold recommendation, five have issued a buy recommendation and one has issued a strong buy recommendation on the company. The average twelve-month price target among brokers that have issued ratings on the stock in the last year is $18.33.
Several equities research analysts have weighed in on the company. HC Wainwright dropped their price objective on Kyverna Therapeutics from $6.00 to $4.00 and set a “neutral” rating for the company in a report on Thursday, April 3rd. Morgan Stanley dropped their price target on Kyverna Therapeutics from $40.00 to $20.00 and set an “overweight” rating for the company in a research note on Tuesday, April 1st.
Institutional Investors Weigh In On Kyverna Therapeutics
Kyverna Therapeutics Stock Performance
Shares of Kyverna Therapeutics stock opened at $1.91 on Tuesday. The company’s 50 day moving average price is $2.67 and its 200-day moving average price is $3.91. Kyverna Therapeutics has a 52-week low of $1.79 and a 52-week high of $24.91. The stock has a market capitalization of $82.54 million, a price-to-earnings ratio of -0.55 and a beta of 2.57.
Kyverna Therapeutics (NASDAQ:KYTX – Get Free Report) last released its quarterly earnings data on Thursday, March 27th. The company reported ($0.88) earnings per share (EPS) for the quarter, missing analysts’ consensus estimates of ($0.87) by ($0.01). As a group, equities research analysts forecast that Kyverna Therapeutics will post -3.29 earnings per share for the current fiscal year.
Kyverna Therapeutics Company Profile
Kyverna Therapeutics, Inc, a clinical-stage biopharmaceutical company, focuses on developing cell therapies for patients suffering from autoimmune diseases. Its lead product candidate is KYV-101, an autologous CD19 CAR T-cell product candidate for the treatment of patients with lupus nephritis and systemic sclerosis that is in Phase I clinical trial; and for myasthenia gravis and multiple sclerosis that is in Phase II clinical trial.
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