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CRSP CRISPR Therapeutics AG

55.56
0.00 (0.00%)
Pre Market
Last Updated: 04:04:55
Delayed by 15 minutes

Period:

Draw Mode:

Volume 40
Bid Price 55.68
Ask Price 55.75
News -
Day High

Low
37.55

52 Week Range

High
91.10

Day Low
Company Name Stock Ticker Symbol Market Type
CRISPR Therapeutics AG CRSP NASDAQ Common Stock
  Price Change Change Percent Stock Price Last Traded
0.00 0.00% 55.56 04:04:55
Open Price Low Price High Price Close Price Prev Close
55.56
Trades Volume Avg Volume 52 Week Range
8 40 - 37.55 - 91.10
Last Trade Time Type Quantity Stock Price Currency
04:16:39 5 $ 55.75 USD

CRISPR Therapeutics (CRSP) Options Flow Summary

Overall Flow

Bearish

Net Premium

-18M

Calls / Puts

30.77%

Buys / Sells

95.83%

OTM / ITM

8.51%

Sweeps Ratio

0.02%

CRISPR Therapeutics AG Financials

Market Cap Shares in Issue Float Revenue Profit/Loss EPS PE Ratio
4.46B 80.28M - 371.21M -153.61M -1.91 -
Short Interest Dividends Per Share Dividend Yield Ex-Div Date Insider B/S Insider % Owned
- - - -

more financials information »

CRISPR Therapeutics News

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Historical CRSP Price Data

Period Open High Low VWAP Avg. Daily Vol Change %
1 Week62.7063.0855.5258.901,234,742-7.14-11.39%
1 Month73.7875.9155.5264.921,260,482-18.22-24.70%
3 Months62.8791.1055.5274.081,769,007-7.31-11.63%
6 Months43.4391.1037.5565.302,359,61112.1327.93%
1 Year54.7991.1037.5561.901,738,8190.771.41%
3 Years117.12169.6737.5571.751,505,472-61.56-52.56%
5 Years36.73220.2132.0080.151,343,40018.8351.27%

CRISPR Therapeutics Description

CRISPR Therapeutics is a gene editing company focused on the development of CRISPR/Cas9-based therapeutics. CRISPR/Cas9 stands for Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9), which is a revolutionary technology for precisely altering specific sequences of genomic DNA. The company is focused on using this technology to treat genetically defined diseases. CRISPR's most advanced pipeline candidate, CTX001, is in collaboration with Vertex Pharmaceuticals and targets sickle cell disease and transfusion-dependent beta-thalassemia, which have high unmet medical needs. The company is progressing additional gene editing programs for immuno-oncology, as well as a stem cell-derived therapy for the treatment of Type 1 diabetes.

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