Compugen Ltd. (NASDAQ:CGEN – Get Free Report) was the target of a significant decline in short interest during the month of October. As of October 31st, there was short interest totalling 1,270,000 shares, a decline of 18.1% from the October 15th total of 1,550,000 shares. Based on an average daily trading volume, of 225,400 shares, the short-interest ratio is presently 5.6 days.
Wall Street Analyst Weigh In
Separately, StockNews.com upgraded shares of Compugen from a “hold” rating to a “buy” rating in a report on Thursday, August 15th.
View Our Latest Stock Report on CGEN
Institutional Inflows and Outflows
Compugen Stock Down 5.4 %
Shares of Compugen stock opened at $1.41 on Friday. The business has a fifty day simple moving average of $1.75 and a 200 day simple moving average of $1.87. The stock has a market cap of $125.82 million, a PE ratio of 70.50 and a beta of 2.64. Compugen has a 12 month low of $0.61 and a 12 month high of $3.03.
Compugen (NASDAQ:CGEN – Get Free Report) last posted its earnings results on Tuesday, November 12th. The biotechnology company reported $0.01 earnings per share (EPS) for the quarter, missing the consensus estimate of $0.21 by ($0.20). The company had revenue of $17.13 million for the quarter, compared to analyst estimates of $17.67 million. Compugen had a return on equity of 2.62% and a net margin of 2.67%. During the same quarter in the previous year, the firm posted ($0.11) earnings per share. Analysts expect that Compugen will post 0.07 EPS for the current fiscal year.
About Compugen
Compugen Ltd., a clinical-stage therapeutic discovery and development company, researches, develops, and commercializes therapeutic and product candidates in Israel, the United States, and Europe. The company’s immuno-oncology pipeline consists of COM701, an anti-PVRIG antibody that is in Phase I clinical study used for the treatment of solid tumors; COM902, a therapeutic antibody targeting TIGIT, which is in Phase I monotherapy clinical study in patients with advanced malignancies through sequential dose escalations; Bapotulimab, a therapeutic antibody targeting ILDR2 that is in Phase I clinical study in patients with naïve head and neck squamous cell carcinoma; and Rilvegostomig, a novel anti-TIGIT/PD-1 bispecific antibody, which is in Phase II clinical study in patients with advanced or metastatic non-small cell lung cancer.
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