Biofrontera Inc. (NASDAQ:BFRI – Get Free Report) was the recipient of a large decrease in short interest during the month of February. As of February 27th, there was short interest totaling 150,744 shares, a decrease of 65.5% from the February 12th total of 436,863 shares. Based on an average daily volume of 184,747 shares, the short-interest ratio is currently 0.8 days. Currently, 1.4% of the shares of the stock are sold short. Currently, 1.4% of the shares of the stock are sold short. Based on an average daily volume of 184,747 shares, the short-interest ratio is currently 0.8 days.
Analyst Ratings Changes
Separately, Benchmark reiterated a “buy” rating on shares of Biofrontera in a report on Friday, November 14th. One equities research analyst has rated the stock with a Buy rating and one has assigned a Sell rating to the company’s stock. Based on data from MarketBeat.com, Biofrontera currently has a consensus rating of “Hold” and an average price target of $2.75.
Get Our Latest Research Report on Biofrontera
Institutional Trading of Biofrontera
Biofrontera Trading Down 0.2%
BFRI stock traded down $0.00 during midday trading on Friday, reaching $0.87. The stock had a trading volume of 47,678 shares, compared to its average volume of 560,425. Biofrontera has a 52-week low of $0.54 and a 52-week high of $1.19. The company’s fifty day simple moving average is $0.86 and its 200 day simple moving average is $0.88. The company has a market cap of $10.11 million, a price-to-earnings ratio of -0.53 and a beta of 0.61.
Biofrontera Company Profile
Biofrontera AG is a specialty biopharmaceutical company focused on the research, development and commercialization of products for dermatological applications. The company’s core expertise lies in photodynamic therapy (PDT), a treatment modality that uses a photosensitizing agent activated by a specific light source to target diseased skin cells while sparing surrounding healthy tissue.
The flagship product in Biofrontera’s portfolio is Ameluz (aminolevulinic acid hydrochloride 10 % gel), which has received marketing approval in the European Union for treatment of actinic keratosis and basal cell carcinoma, and in the United States for actinic keratosis.
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