Revance Therapeutics, Inc. (NASDAQ:RVNC – Get Free Report) has been given a consensus rating of “Hold” by the nine analysts that are presently covering the stock, Marketbeat reports. Eight 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 brokerages that have covered the stock in the last year is $8.39.
RVNC has been the subject of a number of analyst reports. HC Wainwright restated a “neutral” rating and set a $6.60 price target on shares of Revance Therapeutics in a research note on Friday, November 8th. Needham & Company LLC restated a “hold” rating on shares of Revance Therapeutics in a research report on Friday, January 17th. Barclays decreased their price target on Revance Therapeutics from $7.00 to $3.00 and set an “equal weight” rating on the stock in a research note on Monday, December 23rd. StockNews.com began coverage on Revance Therapeutics in a research note on Friday, February 14th. They set a “hold” rating for the company. Finally, Mizuho lowered their target price on shares of Revance Therapeutics from $6.66 to $3.10 and set a “neutral” rating on the stock in a report on Tuesday, December 10th.
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Revance Therapeutics Stock Performance
NASDAQ:RVNC opened at $3.65 on Thursday. The company has a 50-day moving average of $3.40 and a 200-day moving average of $4.57. Revance Therapeutics has a 52 week low of $2.30 and a 52 week high of $7.56. The company has a market capitalization of $381.02 million, a price-to-earnings ratio of -1.89 and a beta of 0.90.
Revance Therapeutics Company Profile
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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