Sangamo Therapeutics (NASDAQ:SGMO – Get Free Report) is projected to announce its Q2 2025 earnings results after the market closes on Thursday, August 7th. Analysts expect the company to announce earnings of ($0.07) per share and revenue of $31.68 million for the quarter.
Sangamo Therapeutics (NASDAQ:SGMO – Get Free Report) last announced its earnings results on Monday, May 12th. The biopharmaceutical company reported ($0.14) EPS for the quarter, missing analysts’ consensus estimates of ($0.11) by ($0.03). The business had revenue of $6.44 million during the quarter, compared to analyst estimates of $7.90 million. Sangamo Therapeutics had a negative net margin of 124.61% and a negative return on equity of 345.98%. On average, analysts expect Sangamo Therapeutics to post $0 EPS for the current fiscal year and $0 EPS for the next fiscal year.
Sangamo Therapeutics Price Performance
Shares of NASDAQ:SGMO opened at $0.54 on Tuesday. Sangamo Therapeutics has a 1-year low of $0.41 and a 1-year high of $3.18. The stock has a market cap of $124.75 million, a P/E ratio of -1.37 and a beta of 1.18. The firm has a fifty day moving average price of $0.51 and a 200 day moving average price of $0.74.
Analyst Upgrades and Downgrades
Read Our Latest Stock Report on Sangamo Therapeutics
Sangamo Therapeutics Company Profile
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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