Shares of Geron Corporation (NASDAQ:GERN – Get Free Report) have been given a consensus recommendation of “Hold” by the ten brokerages that are presently covering the firm, Marketbeat reports. Two analysts have rated the stock with a sell rating, four have given a hold rating and four have given a buy rating to the company. The average 1-year price target among analysts that have covered the stock in the last year is $2.75.
Several equities research analysts recently weighed in on the stock. Needham & Company LLC cut their target price on shares of Geron from $5.00 to $4.00 and set a “buy” rating on the stock in a research note on Wednesday, November 5th. HC Wainwright reaffirmed a “neutral” rating on shares of Geron in a research report on Tuesday, December 9th. TD Cowen reiterated a “buy” rating on shares of Geron in a report on Thursday, January 29th. Weiss Ratings reissued a “sell (e+)” rating on shares of Geron in a research note on Wednesday, January 28th. Finally, UBS Group reaffirmed a “neutral” rating on shares of Geron in a research report on Tuesday, December 9th.
Read Our Latest Analysis on GERN
Hedge Funds Weigh In On Geron
Geron Stock Performance
NASDAQ GERN opened at $1.95 on Wednesday. The company has a debt-to-equity ratio of 0.48, a current ratio of 5.96 and a quick ratio of 4.87. The company has a market cap of $1.24 billion, a P/E ratio of -16.25 and a beta of 0.62. The stock has a 50-day moving average of $1.46 and a two-hundred day moving average of $1.35. Geron has a 1-year low of $1.04 and a 1-year high of $2.42.
About Geron
Geron Corporation (NASDAQ: GERN) is a clinical-stage biotechnology company dedicated to developing and commercializing novel treatments that target telomerase, an enzyme critical to cancer cell immortality. The company’s research is focused on hematologic malignancies and solid tumors, with a pipeline designed to address diseases that have historically had limited therapeutic options.
The lead product candidate, imetelstat, is a first-in-class telomerase inhibitor currently in Phase II and Phase III clinical trials for myelofibrosis and myelodysplastic syndromes.
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