Shares of Dicerna Pharmaceuticals, Inc. (NASDAQ:DRNA) reached a new 52-week high on Wednesday . The company traded as high as $9.40 and last traded at $8.26, with a volume of 138000 shares trading hands. The stock had previously closed at $7.95.
A number of research firms have recently weighed in on DRNA. ValuEngine lowered Dicerna Pharmaceuticals from a “hold” rating to a “sell” rating in a research note on Tuesday, August 1st. Zacks Investment Research lowered Dicerna Pharmaceuticals from a “hold” rating to a “sell” rating in a research note on Tuesday, August 22nd. HC Wainwright restated a “buy” rating and set a $10.00 target price (up previously from $6.00) on shares of Dicerna Pharmaceuticals in a report on Friday, November 3rd. Finally, Chardan Capital restated a “hold” rating on shares of Dicerna Pharmaceuticals in a report on Monday, August 14th. Three analysts have rated the stock with a hold rating and three have assigned a buy rating to the stock. The stock presently has a consensus rating of “Buy” and an average target price of $6.81.
Dicerna Pharmaceuticals (NASDAQ:DRNA) last announced its earnings results on Thursday, November 2nd. The biopharmaceutical company reported ($0.92) EPS for the quarter, missing analysts’ consensus estimates of ($0.70) by ($0.22). The business had revenue of $0.47 million for the quarter. Dicerna Pharmaceuticals had a negative net margin of 5,895.26% and a negative return on equity of 293.25%. The firm’s quarterly revenue was up 192.6% compared to the same quarter last year. During the same period in the previous year, the company posted ($0.68) EPS. sell-side analysts expect that Dicerna Pharmaceuticals, Inc. will post -3.04 EPS for the current year.
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About Dicerna Pharmaceuticals
Dicerna Pharmaceuticals, Inc is a ribonucleic acid (RNA) interference-based biopharmaceutical company. The Company operates in the segment of discovery, research and development of treatments based on its RNA interference (RNAi) technology platform. The Company is focused on the discovery and development of treatments for rare inherited diseases involving the liver and for cancers that are genetically defined.
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