CRISPR Therapeutics AG (NASDAQ:CRSP – Get Free Report) shares shot up 8% during mid-day trading on Friday after Needham & Company LLC raised their price target on the stock from $80.00 to $82.00. Needham & Company LLC currently has a buy rating on the stock. CRISPR Therapeutics traded as high as $52.78 and last traded at $52.85. 415,556 shares traded hands during trading, a decline of 76% from the average session volume of 1,723,382 shares. The stock had previously closed at $48.93.
Several other research firms have also weighed in on CRSP. Bank of America lowered their price target on CRISPR Therapeutics from $90.00 to $89.00 and set a “buy” rating on the stock in a research report on Thursday, January 22nd. Citizens Jmp decreased their target price on shares of CRISPR Therapeutics from $86.00 to $80.00 and set a “market outperform” rating for the company in a research note on Friday, January 30th. Chardan Capital lowered their target price on shares of CRISPR Therapeutics from $82.00 to $74.00 and set a “buy” rating on the stock in a report on Wednesday, November 26th. Royal Bank Of Canada increased their price target on shares of CRISPR Therapeutics from $42.00 to $50.00 and gave the company a “sector perform” rating in a research note on Tuesday, November 11th. Finally, Wedbush decreased their price objective on shares of CRISPR Therapeutics from $13.00 to $9.00 and set an “outperform” rating for the company in a research report on Wednesday, November 5th. Twelve research analysts have rated the stock with a Buy rating, seven have given a Hold rating and two have assigned a Sell rating to the stock. Based on data from MarketBeat, the company presently has an average rating of “Hold” and an average target price of $67.94.
Read Our Latest Research Report on CRSP
Insider Buying and Selling
Hedge Funds Weigh In On CRISPR Therapeutics
Institutional investors and hedge funds have recently made changes to their positions in the company. Ramirez Asset Management Inc. acquired a new position in CRISPR Therapeutics in the 4th quarter valued at $26,000. Optiver Holding B.V. boosted its position in shares of CRISPR Therapeutics by 71.4% in the third quarter. Optiver Holding B.V. now owns 504 shares of the company’s stock valued at $33,000 after acquiring an additional 210 shares during the period. Thompson Investment Management Inc. acquired a new position in shares of CRISPR Therapeutics in the third quarter valued at about $33,000. Strategic Advocates LLC bought a new position in CRISPR Therapeutics during the third quarter worth about $34,000. Finally, Rothschild Investment LLC increased its position in CRISPR Therapeutics by 836.7% during the fourth quarter. Rothschild Investment LLC now owns 562 shares of the company’s stock worth $29,000 after acquiring an additional 502 shares during the period. Institutional investors and hedge funds own 69.20% of the company’s stock.
CRISPR Therapeutics Trading Up 8.7%
The firm has a market cap of $5.07 billion, a price-to-earnings ratio of -9.52 and a beta of 1.72. The firm’s 50 day simple moving average is $54.29 and its two-hundred day simple moving average is $57.44.
CRISPR Therapeutics (NASDAQ:CRSP – Get Free Report) last announced its earnings results on Thursday, February 12th. The company reported ($1.37) earnings per share (EPS) for the quarter, missing analysts’ consensus estimates of ($1.15) by ($0.22). CRISPR Therapeutics had a negative return on equity of 21.23% and a negative net margin of 1,273.70%.The business had revenue of $0.86 million for the quarter, compared to analyst estimates of $4.72 million. During the same quarter in the previous year, the company earned ($1.01) EPS. The business’s revenue for the quarter was down 97.8% on a year-over-year basis. As a group, equities research analysts anticipate that CRISPR Therapeutics AG will post -5.16 earnings per share for the current fiscal 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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