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CRSP

Equity

CRISPR Therapeutics AG

Health Care · Biotechnology

$59.17

+59.17 (+0.00%)

Open

N/A

Day Range

$57.75 - $60.46

52W Range

$30.04 - $78.48

Volume

387K

Price History

Key Statistics

Market Cap

N/A

P/E Ratio

N/A

EPS

N/A

Dividend Yield

N/A

P/B Ratio

N/A

Payout Ratio

N/A

ROE

N/A

Debt/Equity

N/A

Peers in Health Care

Symbol Name Price Mkt Cap Div Yield Change
ABBV AbbVie Inc. $233.86 N/A 2.84% +0.00%
AKBA Akebia Therapeutics, Inc. $1.27 N/A - +0.00%
ACAD ACADIA Pharmaceuticals Inc. $22.50 N/A - +0.00%
001540.KQ AHN-GOOK PHA $7,280.00 N/A 6.04% +0.00%
ABCL AbCellera Biologics Inc. $3.66 N/A - +0.00%
A Agilent Technologies, Inc. $120.25 N/A 0.83% +0.00%
ABT Abbott Laboratories $113.84 N/A 2.11% +0.00%
ACB Aurora Cannabis Inc. $3.68 N/A - +0.00%

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About CRISPR Therapeutics AG

CRISPR Therapeutics AG, a gene editing company, focuses on developing gene-based medicines for serious human diseases using its Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) platform. The company's CRISPR/Cas9 is a technology for gene editing which is the process of precisely altering specific sequences of genomic DNA. It has a portfolio of therapeutic programs across a range of disease areas, including hemoglobinopathies, CAR T cell therapies, in vivo, and type 1 diabetes, as well as develops investigational CAR T programs, including an autologous, gene-edited CAR T program targeting allogeneic chimeric antigen receptor T cell for autoimmune indications and oncology. The company's lead product candidate is CASGEVY, an ex vivo CRISPR/Cas9 gene-edited cell therapy for treating patients suffering from transfusion-dependent beta-thalassemia, severe sickle cell disease (SCD), and hemoglobinopathies in which a patient's hematopoietic stem and progenitor cells are edited to produce high levels of fetal hemoglobin in red blood cells. It also develops CAR T cell therapies, including CTX112 targeting cluster of differentiation 19 (CD19) and CTX131 targeting CD70 for oncology and autoimmune indications; CTX310 and CTX320, in vivo gene editing to address the cardiovascular disease by disrupting the validated targets angiopoietin-like protein 3 and lipoprotein; and CTX211, an allogeneic, gene-edited, hypoimmune stem cell-derived product candidate for the treatment of T1D. It has strategic partnerships with Vertex Pharmaceuticals Incorporated. CRISPR Therapeutics AG was incorporated in 2013 and is headquartered in Zug, Switzerland.

www.crisprtx.com →

🐂 Bull Score

Our proprietary rating measures dividend reliability based on 6 fundamental factors including payout sustainability, financial strength, and cash flow coverage.

F 0/100

Very Risky

Bull Score

- No consecutive dividend growth 0/25
- Negative profit margin 0/15
Limited data — score may change as more metrics become available

Dividend Safety

Assessment based on payout ratio, debt levels, profit margins, and dividend growth track record.

35

Unsafe

Based on 4 fundamental factors

- Negative profit margin

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