Sarepta Therapeutics, Inc. (NASDAQ:SRPT – Get Free Report) has been given a consensus rating of “Moderate Buy” by the twenty-two ratings firms that are currently covering the stock, MarketBeat reports. One equities research analyst has rated the stock with a sell rating, one has assigned a hold rating, nineteen have given a buy rating and one has given a strong buy rating to the company. The average 1-year price objective among brokerages that have issued a report on the stock in the last year is $178.71.
A number of analysts have recently issued reports on SRPT shares. Needham & Company LLC lowered their price objective on shares of Sarepta Therapeutics from $205.00 to $202.00 and set a “buy” rating on the stock in a report on Wednesday, November 27th. UBS Group lifted their price target on shares of Sarepta Therapeutics from $173.00 to $188.00 and gave the company a “buy” rating in a research note on Tuesday, September 17th. Cantor Fitzgerald upgraded shares of Sarepta Therapeutics from a “neutral” rating to an “overweight” rating and increased their price objective for the stock from $152.00 to $167.00 in a research note on Thursday, November 7th. Evercore ISI decreased their price objective on Sarepta Therapeutics from $179.00 to $170.00 and set an “outperform” rating for the company in a report on Thursday, November 7th. Finally, Guggenheim upped their target price on Sarepta Therapeutics from $148.00 to $150.00 and gave the stock a “buy” rating in a report on Thursday, November 7th.
Check Out Our Latest Analysis on SRPT
Insider Buying and Selling
Institutional Investors Weigh In On Sarepta Therapeutics
Large investors have recently added to or reduced their stakes in the stock. Nkcfo LLC acquired a new position in Sarepta Therapeutics in the 2nd quarter valued at $43,000. Sunbelt Securities Inc. increased its position in shares of Sarepta Therapeutics by 446.2% in the third quarter. Sunbelt Securities Inc. now owns 284 shares of the biotechnology company’s stock worth $35,000 after purchasing an additional 232 shares during the period. Huntington National Bank raised its stake in Sarepta Therapeutics by 150.9% in the third quarter. Huntington National Bank now owns 291 shares of the biotechnology company’s stock valued at $36,000 after purchasing an additional 175 shares in the last quarter. UMB Bank n.a. lifted its position in Sarepta Therapeutics by 105.9% during the third quarter. UMB Bank n.a. now owns 383 shares of the biotechnology company’s stock worth $48,000 after purchasing an additional 197 shares during the period. Finally, Values First Advisors Inc. acquired a new stake in Sarepta Therapeutics during the third quarter worth about $59,000. Institutional investors and hedge funds own 86.68% of the company’s stock.
Sarepta Therapeutics Stock Up 0.3 %
Shares of Sarepta Therapeutics stock opened at $121.59 on Wednesday. The firm has a market cap of $11.61 billion, a PE ratio of 97.27 and a beta of 0.77. The business’s 50 day simple moving average is $122.85 and its 200 day simple moving average is $131.49. The company has a debt-to-equity ratio of 0.93, a quick ratio of 3.03 and a current ratio of 3.84. Sarepta Therapeutics has a 52-week low of $91.34 and a 52-week high of $173.25.
Sarepta Therapeutics Company Profile
Sarepta Therapeutics, Inc, a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, gene therapies, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 injection to treat duchenne muscular dystrophy (duchenne) in patients with confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; VYONDYS 53 for the treatment of duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping; AMONDYS 45 for the treatment of duchenne in patients with confirmed mutation of the dystrophin gene; and ELEVIDYS, an adeno-associated virus based gene therapy for the treatment of ambulatory pediatric patients aged 4 through 5 years with duchenne with a confirmed mutation in the duchenne gene.
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