Shuttle Pharmaceuticals Holdings, Inc. (NASDAQ:SHPH – Get Free Report) was the recipient of a large decrease in short interest in the month of December. As of December 31st, there was short interest totaling 160,518 shares, a decrease of 42.5% from the December 15th total of 279,178 shares. Based on an average trading volume of 63,451 shares, the short-interest ratio is currently 2.5 days. Currently, 11.5% of the shares of the company are sold short. Currently, 11.5% of the shares of the company are sold short. Based on an average trading volume of 63,451 shares, the short-interest ratio is currently 2.5 days.
Shuttle Pharmaceuticals Stock Performance
SHPH opened at $1.42 on Thursday. The company has a fifty day moving average of $1.81 and a two-hundred day moving average of $3.04. Shuttle Pharmaceuticals has a fifty-two week low of $1.26 and a fifty-two week high of $25.25. The stock has a market capitalization of $2.27 million, a price-to-earnings ratio of -0.12 and a beta of -1.00.
Shuttle Pharmaceuticals (NASDAQ:SHPH – Get Free Report) last announced its earnings results on Thursday, November 13th. The company reported ($1.05) earnings per share (EPS) for the quarter.
Analyst Upgrades and Downgrades
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Institutional Investors Weigh In On Shuttle Pharmaceuticals
A hedge fund recently bought a new stake in Shuttle Pharmaceuticals stock. Connective Capital Management LLC acquired a new stake in shares of Shuttle Pharmaceuticals Holdings, Inc. (NASDAQ:SHPH – Free Report) in the 3rd quarter, according to the company in its most recent disclosure with the SEC. The institutional investor acquired 100,535 shares of the company’s stock, valued at approximately $357,000. Connective Capital Management LLC owned approximately 9.40% of Shuttle Pharmaceuticals at the end of the most recent quarter. 4.58% of the stock is currently owned by institutional investors and hedge funds.
About Shuttle Pharmaceuticals
Shuttle Pharmaceuticals Holdings, Inc, a clinical stage pharmaceutical company, develops novel therapies to cure cancers. It develops Ropidoxuridine, an oral halogenated pyrimidine to treat patients with brain tumors and sarcomas SP-1-161, an HDAC inhibitor that initiates the mutated in ataxia-telangiectasia response pathway for radiation sensitizing cancer cells and protecting normal cells; SP-2-225, a pre-clinical class IIb that effects on the regulation of the immune system; and SP-1-303, a pre-clinical selective Class I HDAC for the treatment of ER positive cancers .
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