Editas Medicine, Inc. (NASDAQ:EDIT – Get Free Report) has received an average recommendation of “Hold” from the fourteen ratings firms that are presently covering the company, MarketBeat reports. Two research analysts have rated the stock with a sell recommendation, nine have issued a hold recommendation and three have assigned a buy recommendation to the company. The average 12-month price target among brokerages that have issued a report on the stock in the last year is $7.00.
A number of analysts have commented on the stock. Truist Financial downgraded shares of Editas Medicine from a “buy” rating to a “hold” rating in a report on Friday, December 13th. Robert W. Baird dropped their price target on shares of Editas Medicine from $10.00 to $8.00 and set an “outperform” rating for the company in a research note on Friday, December 13th. Bank of America cut shares of Editas Medicine from a “buy” rating to an “underperform” rating and dropped their price target for the company from $13.00 to $1.00 in a research note on Monday, November 25th. Wells Fargo & Company cut shares of Editas Medicine from an “overweight” rating to an “equal weight” rating and dropped their price target for the company from $7.00 to $4.00 in a research note on Wednesday, December 11th. Finally, Stifel Nicolaus cut shares of Editas Medicine from a “buy” rating to a “hold” rating and dropped their price target for the company from $11.00 to $3.00 in a research note on Friday, December 13th.
Check Out Our Latest Report on Editas Medicine
Institutional Investors Weigh In On Editas Medicine
Editas Medicine Stock Up 12.2 %
EDIT stock opened at $1.38 on Friday. The company’s 50-day simple moving average is $1.36 and its 200-day simple moving average is $2.69. Editas Medicine has a 52-week low of $1.12 and a 52-week high of $11.58. The firm has a market cap of $113.92 million, a P/E ratio of -0.54 and a beta of 1.94.
Editas Medicine Company Profile
Editas Medicine, Inc, a clinical stage genome editing company, focuses on developing transformative genomic medicines to treat a range of serious diseases. It develops a proprietary gene editing platform based on CRISPR technology. The company develops EDIT-101, which is in Phase 1/2 BRILLIANCE trial for Leber Congenital Amaurosis; and reni-cel, a clinical development gene-edited medicine to treat sickle cell disease and transfusion-dependent beta-thalassemia.
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