Silexion Therapeutics Corp (NASDAQ:SLXN – Get Free Report) was the target of a significant increase in short interest in the month of September. As of September 15th, there was short interest totaling 238,617 shares, an increase of 1,545.5% from the August 31st total of 14,501 shares. Currently, 4.3% of the shares of the stock are sold short. Based on an average trading volume of 15,566,949 shares, the short-interest ratio is presently 0.0 days.
Wall Street Analyst Weigh In
SLXN has been the topic of a number of analyst reports. Weiss Ratings restated a “sell (e+)” rating on shares of Silexion Therapeutics in a research report on Friday, September 11th. Maxim Group cut Silexion Therapeutics from a “strong-buy” rating to a “hold” rating in a report on Wednesday, July 29th. One research analyst has rated the stock with a Buy rating, two have given a Hold rating and one has given a Sell rating to the company’s stock. According to MarketBeat.com, the stock currently has a consensus rating of “Hold”.
Get Our Latest Research Report on SLXN
Silexion Therapeutics Trading Down 18.5%
Silexion Therapeutics (NASDAQ:SLXN – Get Free Report) last issued its quarterly earnings results on Saturday, August 15th. The company reported ($5.17) EPS for the quarter, topping the consensus estimate of ($21.20) by $16.03. On average, equities research analysts forecast that Silexion Therapeutics will post -4.7 earnings per share for the current fiscal year.
Silexion Therapeutics Company Profile
Silexion Therapeutics Ltd. is an Israel-based clinical-stage biotechnology company focused on developing RNA-based treatments for solid tumors driven by mutations in the KRAS gene. The company’s research is centered on gene-silencing technologies designed to inhibit KRAS, an important cancer-promoting protein that has historically been difficult to target with conventional therapies.
Silexion’s development programs include SIL-204, an investigational small interfering RNA (siRNA) therapy designed to target KRAS mutations, including KRAS G12D, a frequently observed mutation in pancreatic cancer.
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