
CRISPR Therapeutics AG (CRSP)
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Learn more- Previous Close
52.34 - Open
51.59 - Bid 37.08 x 100
- Ask 65.95 x 100
- Day's Range
50.60 - 52.55 - 52 Week Range
33.03 - 78.48 - Volume
1,034,560 - Avg. Volume
1,902,085 - Market Cap (intraday)
4.979B - Beta (5Y Monthly) 1.79
- PE Ratio (TTM)
-- - EPS (TTM)
-6.47 - Earnings Date (est.) May 11, 2026
- Forward Dividend & Yield --
- Ex-Dividend Date --
- 1y Target Est
83.35
Recent News: CRSP
View MorePerformance Overview: CRSP
Trailing total returns as of 5/1/2026, which may include dividends or other distributions. Benchmark is S&P 500 (^GSPC) .
YTD Return
1-Year Return
3-Year Return
5-Year Return
Earnings Trends: CRSP
View MoreAnalyst Insights: CRSP
View MoreStatistics: CRSP
View MoreValuation Measures
-
Market Cap
4.98B
-
Enterprise Value
3.21B
-
Trailing P/E
--
-
Forward P/E
--
-
PEG Ratio (5yr expected)
--
-
Price/Sales (ttm)
122.27
-
Price/Book (mrq)
2.59
-
Enterprise Value/Revenue
84.52
-
Enterprise Value/EBITDA
--
Financial Highlights
Profitability and Income Statement
-
Profit Margin
0.00%
-
Return on Assets (ttm)
-15.76%
-
Return on Equity (ttm)
-30.18%
-
Revenue (ttm)
3.51M
-
Net Income Avi to Common (ttm)
-581.6M
-
Diluted EPS (ttm)
-6.47
Balance Sheet and Cash Flow
-
Total Cash (mrq)
1.98B
-
Total Debt/Equity (mrq)
10.76%
-
Levered Free Cash Flow (ttm)
-205.62M
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Company Insights: CRSP
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Dividend Score
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Insider Sentiment Score
Research Reports: CRSP
View More-
Positive Long-Term Outlook for Crispr Therapeutics as Gene Editing Portfolio Makes Progress
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 first approved drug is Casgevy, which was developed in collaboration with Vertex Pharmaceuticals and targets sickle-cell disease and transfusion-dependent beta-thalassemia. The company is advancing a variety of gene editing programs in immuno-oncology, cardiovascular, and a stem cell-derived therapy to treat Type 1 diabetes.
RatingPrice Target -
Positive Long-Term Outlook for Crispr Therapeutics as Gene Editing Portfolio Makes Progress
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 first approved drug is Casgevy, which was developed in collaboration with Vertex Pharmaceuticals and targets sickle-cell disease and transfusion-dependent beta-thalassemia. The company is advancing a variety of gene editing programs in immuno-oncology, cardiovascular, and a stem cell-derived therapy to treat Type 1 diabetes.
RatingPrice Target -
Crispr Earnings: Casgevy Sees Stronger Uptake as Early-Stage Pipeline Assets Make Progress
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 first approved drug is Casgevy, which was developed in collaboration with Vertex Pharmaceuticals and targets sickle-cell disease and transfusion-dependent beta-thalassemia, which have high unmet medical needs. The company is advancing a variety of gene editing programs in immuno-oncology, cardiovascular, and a stem cell-derived therapy to treat Type 1 diabetes.
RatingPrice Target -
Crispr Earnings: Casgevy Sees Stronger Uptake as Early-Stage Pipeline Assets Make Progress
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 first approved drug is Casgevy, which was developed in collaboration with Vertex Pharmaceuticals and targets sickle-cell disease and transfusion-dependent beta-thalassemia, which have high unmet medical needs. The company is advancing a variety of gene editing programs in immuno-oncology, cardiovascular, and a stem cell-derived therapy to treat Type 1 diabetes.
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