CRISPR Therapeutics AG (NASDAQ:CRSP – Get Free Report) has been given a consensus recommendation of “Moderate Buy” by the nineteen ratings firms that are currently covering the firm, Marketbeat reports. Two analysts have rated the stock with a sell recommendation, six have issued a hold recommendation, ten have given a buy recommendation and one has issued a strong buy recommendation on the company. The average 12-month price objective among brokers that have issued ratings on the stock in the last year is $65.4706.
Several brokerages have recently issued reports on CRSP. Sanford C. Bernstein boosted their price target on shares of CRISPR Therapeutics from $50.00 to $56.00 and gave the company a “market perform” rating in a report on Wednesday. Bank of America reduced their price target on shares of CRISPR Therapeutics from $90.00 to $89.00 and set a “buy” rating for the company in a report on Thursday, January 22nd. Wall Street Zen raised shares of CRISPR Therapeutics from a “sell” rating to a “hold” rating in a report on Saturday, May 9th. Weiss Ratings reaffirmed a “sell (d-)” rating on shares of CRISPR Therapeutics in a report on Monday, April 20th. Finally, Citizens Jmp reduced their price objective on shares of CRISPR Therapeutics from $86.00 to $80.00 and set a “market outperform” rating for the company in a report on Friday, January 30th.
View Our Latest Stock Report on CRISPR Therapeutics
Insider Buying and Selling
Institutional Investors Weigh In On CRISPR Therapeutics
Several institutional investors have recently bought and sold shares of CRSP. GSK plc acquired a new stake in CRISPR Therapeutics in the fourth quarter worth about $168,890,000. Orbis Allan Gray Ltd raised its position in CRISPR Therapeutics by 76.9% in the second quarter. Orbis Allan Gray Ltd now owns 2,764,532 shares of the company’s stock worth $134,467,000 after acquiring an additional 1,201,600 shares in the last quarter. SR One Capital Management LP raised its position in CRISPR Therapeutics by 94.4% in the third quarter. SR One Capital Management LP now owns 2,038,763 shares of the company’s stock worth $132,132,000 after acquiring an additional 989,812 shares in the last quarter. State Street Corp raised its position in CRISPR Therapeutics by 35.6% in the second quarter. State Street Corp now owns 3,270,596 shares of the company’s stock worth $159,082,000 after acquiring an additional 859,334 shares in the last quarter. Finally, ARK Investment Management LLC raised its position in CRISPR Therapeutics by 7.5% in the fourth quarter. ARK Investment Management LLC now owns 10,522,057 shares of the company’s stock worth $551,777,000 after acquiring an additional 735,084 shares in the last quarter. Institutional investors and hedge funds own 69.20% of the company’s stock.
CRISPR Therapeutics Stock Performance
Shares of CRSP opened at $48.41 on Tuesday. CRISPR Therapeutics has a 1 year low of $35.38 and a 1 year high of $78.48. The company has a market cap of $4.67 billion, a price-to-earnings ratio of -7.78 and a beta of 1.74. The company has a debt-to-equity ratio of 0.32, a quick ratio of 17.96 and a current ratio of 17.97. The firm has a fifty day moving average of $51.49 and a 200-day moving average of $53.77.
CRISPR Therapeutics (NASDAQ:CRSP – Get Free Report) last announced its quarterly earnings results on Tuesday, March 31st. The company reported ($1.28) earnings per share (EPS) for the quarter. CRISPR Therapeutics had a negative net margin of 13,856.54% and a negative return on equity of 25.66%. The firm had revenue of $1.46 million for the quarter. As a group, equities analysts anticipate that CRISPR Therapeutics will post -5.08 earnings per share for the current year.
CRISPR Therapeutics Company Profile
CRISPR Therapeutics AG is a biopharmaceutical company specializing in the development of gene-editing therapies based on the CRISPR/Cas9 platform. The company applies its proprietary technology to modify genes in human cells, aiming to create durable treatments for a range of serious diseases. Its research and development efforts focus on both ex vivo and in vivo applications, enabling targeted correction or disruption of disease-causing genes.
Among its lead programs is CTX001, an ex vivo edited cell therapy designed to treat sickle cell disease and transfusion-dependent β-thalassemia in collaboration with Vertex Pharmaceuticals.
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