Shares of Editas Medicine, Inc. (NASDAQ:EDIT – Get Free Report) have received a consensus rating of “Hold” from the fourteen brokerages that are currently covering the firm, MarketBeat reports. Two equities research analysts have rated the stock with a sell recommendation, nine have assigned a hold recommendation and three have issued a buy recommendation on the company. The average 12 month price objective among brokers that have covered the stock in the last year is $7.00.
EDIT has been the subject of several recent analyst reports. Evercore ISI reduced their price objective on shares of Editas Medicine from $7.00 to $5.00 and set an “outperform” rating for the company in a research report on Monday, December 16th. Stifel Nicolaus downgraded shares of Editas Medicine from a “buy” rating to a “hold” rating and reduced their price target for the company from $11.00 to $3.00 in a research report on Friday, December 13th. Robert W. Baird dropped their price objective on shares of Editas Medicine from $10.00 to $8.00 and set an “outperform” rating on the stock in a research note on Friday, December 13th. JPMorgan Chase & Co. cut shares of Editas Medicine from a “neutral” rating to an “underweight” rating in a research note on Monday, December 16th. Finally, Truist Financial cut shares of Editas Medicine from a “buy” rating to a “hold” rating in a research note on Friday, December 13th.
Read Our Latest Analysis on Editas Medicine
Institutional Trading of Editas Medicine
Editas Medicine Stock Performance
Shares of EDIT stock opened at $1.38 on Friday. The stock has a market capitalization of $113.92 million, a P/E ratio of -0.54 and a beta of 1.94. The company has a 50 day moving average price of $1.34 and a 200 day moving average price of $2.62. Editas Medicine has a fifty-two week low of $1.12 and a fifty-two week high of $11.58.
About Editas Medicine
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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