Shares of Sangamo Therapeutics, Inc. (NASDAQ:SGMO – Get Free Report) have received an average rating of “Moderate Buy” from the six ratings firms that are presently covering the firm, Marketbeat.com reports. Two research analysts have rated the stock with a hold rating and four have issued a buy rating on the company. The average twelve-month target price among analysts that have updated their coverage on the stock in the last year is $5.17.
SGMO has been the topic of a number of research analyst reports. Truist Financial lowered their target price on Sangamo Therapeutics from $7.00 to $5.00 and set a “buy” rating on the stock in a report on Thursday, January 23rd. Barclays lifted their target price on Sangamo Therapeutics from $3.00 to $9.00 and gave the stock an “overweight” rating in a report on Thursday, November 14th. Wells Fargo & Company lowered their target price on Sangamo Therapeutics from $3.00 to $2.00 and set an “equal weight” rating on the stock in a report on Tuesday, December 31st. HC Wainwright reaffirmed a “buy” rating and set a $10.00 target price on shares of Sangamo Therapeutics in a report on Monday, January 27th. Finally, Jefferies Financial Group lowered their target price on Sangamo Therapeutics from $7.00 to $3.00 and set a “buy” rating on the stock in a report on Tuesday, December 31st.
Check Out Our Latest Research Report on SGMO
Hedge Funds Weigh In On Sangamo Therapeutics
Sangamo Therapeutics Stock Performance
Shares of SGMO opened at $0.96 on Wednesday. The firm has a market capitalization of $199.49 million, a price-to-earnings ratio of -1.27 and a beta of 1.30. Sangamo Therapeutics has a one year low of $0.30 and a one year high of $3.18. The stock’s fifty day moving average is $1.38 and its 200-day moving average is $1.40.
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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