Sangamo Therapeutics, Inc. (NASDAQ:SGMO – Get Free Report) has been assigned an average rating of “Moderate Buy” from the six ratings firms that are currently covering the firm, MarketBeat reports. Three analysts have rated the stock with a hold recommendation and three have given a buy recommendation to the company. The average 1-year price target among brokers that have covered the stock in the last year is $5.67.
SGMO has been the subject of several recent research reports. HC Wainwright reaffirmed a “buy” rating and set a $5.00 target price on shares of Sangamo Therapeutics in a report on Wednesday, May 15th. StockNews.com initiated coverage on shares of Sangamo Therapeutics in a report on Friday. They set a “sell” rating for the company.
View Our Latest Stock Report on Sangamo Therapeutics
Institutional Investors Weigh In On Sangamo Therapeutics
Sangamo Therapeutics Trading Up 3.7 %
SGMO opened at $0.45 on Friday. Sangamo Therapeutics has a 12-month low of $0.29 and a 12-month high of $1.67. The firm has a market capitalization of $94.38 million, a PE ratio of -0.24 and a beta of 1.24. The firm has a 50 day moving average of $0.50 and a two-hundred day moving average of $0.61.
Sangamo Therapeutics (NASDAQ:SGMO – Get Free Report) last posted its earnings results on Thursday, May 9th. The biopharmaceutical company reported ($0.27) earnings per share for the quarter, missing the consensus estimate of ($0.22) by ($0.05). The firm had revenue of $0.48 million for the quarter, compared to analysts’ expectations of $8.51 million. Sangamo Therapeutics had a negative net margin of 1,749.06% and a negative return on equity of 182.55%. During the same period last year, the firm earned $0.12 earnings per share. As a group, analysts predict that Sangamo Therapeutics will post -0.55 EPS for the current fiscal year.
About Sangamo Therapeutics
Sangamo Therapeutics, Inc, a clinical-stage genomic medicine company, focuses on translating science into medicines that transform the lives of patients and families afflicted with serious diseases in the United States. The company's clinical-stage product candidates are ST-920, a gene therapy product candidate, which is in Phase 1/2 clinical study for the treatment of Fabry disease; TX200, a chimeric antigen receptor engineered regulatory T cell (CAR-Treg) therapy product candidate that is in Phase 1/2 clinical study for the prevention of immune-mediated rejection in HLA-A2 mismatched kidney transplantation; SB-525, a gene therapy product candidate, which is in Phase 3 clinical trial for the treatment of moderately severe to severe hemophilia A; BIVV003, a zinc finger nuclease gene-edited cell therapy product candidate that is in Phase 1/2 PRECIZN-1 clinical study for the treatment of sickle cell disease.
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