Shares of Revance Therapeutics, Inc. (NASDAQ:RVNC – Get Free Report) have earned an average rating of “Hold” from the nine analysts that are presently covering the stock, MarketBeat Ratings reports. Eight research analysts have rated the stock with a hold rating and one has given a buy rating to the company. The average 1-year price target among analysts that have issued a report on the stock in the last year is $8.39.
A number of research firms have recently issued reports on RVNC. HC Wainwright restated a “neutral” rating and issued a $6.60 price target on shares of Revance Therapeutics in a research report on Friday, November 8th. Barclays dropped their price target on Revance Therapeutics from $7.00 to $3.00 and set an “equal weight” rating for the company in a research report on Monday, December 23rd. Needham & Company LLC restated a “hold” rating on shares of Revance Therapeutics in a research report on Friday, January 17th. StockNews.com began coverage on Revance Therapeutics in a research report on Saturday, February 22nd. They issued a “hold” rating for the company. Finally, Mizuho dropped their price target on Revance Therapeutics from $6.66 to $3.10 and set a “neutral” rating for the company in a research report on Tuesday, December 10th.
Get Our Latest Analysis on Revance Therapeutics
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Revance Therapeutics Stock Performance
NASDAQ:RVNC opened at $3.65 on Thursday. Revance Therapeutics has a 12 month low of $2.30 and a 12 month high of $7.56. The stock has a 50 day moving average of $3.45 and a two-hundred day moving average of $4.59. The firm has a market cap of $381.02 million, a P/E ratio of -1.89 and a beta of 0.90.
About Revance Therapeutics
Revance Therapeutics, Inc, a biotechnology company, engages in the development, manufacture, and commercialization of neuromodulators for various aesthetic and therapeutic indications in the United States and internationally. The company’s lead drug candidate is DAXXIFY (DaxibotulinumtoxinA-lanm) for injection for the treatment of glabellar lines and cervical dystonia; has completed phase II clinical trials to treat upper facial lines, moderate or severe dynamic forehead lines, and moderate or severe lateral canthal lines; and has completed Phase II clinical trials for the treatment of adult upper limb spasticity and plantar fasciitis.
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