CRISPR/$CRSP

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About CRISPR

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.

Ticker

$CRSP
Primary listing

Industry

Biotechnology

Headquarters

Zug, Switzerland

Employees

393

ISIN

CH0334081137

CRISPR Metrics

BasicAdvanced
$5.5B
-
-$4.52
1.87
-

What the Analysts think about CRISPR

Analyst ratings (Buy, Hold, Sell) for CRISPR stock.

Bulls say / Bears say

CRISPR Therapeutics' lead product, Casgevy, received FDA approval in December 2023 for treating sickle cell disease and beta-thalassemia, marking the first approval of a CRISPR-based gene-editing therapy. This milestone positions the company at the forefront of gene-editing treatments, potentially opening significant market opportunities. (Nasdaq)
The company's in vivo editing programs, including CTX310 and CTX320, aim to edit genes directly within the body, potentially offering more accessible and scalable treatments compared to ex vivo approaches. Success in these programs could dramatically expand the range of treatable diseases and patient populations. (Investing.com)
Strategic partnerships with industry leaders like Vertex Pharmaceuticals, Nkarta, and Capsida Biotherapeutics enhance CRISPR Therapeutics' research capabilities and expand its therapeutic portfolio, bolstering its position in the biotech sector. (DirectorsTalk Interviews)
Despite the approval of Casgevy, CRISPR Therapeutics has reported significant operating losses, with a net loss of $150.7 million in 2023, indicating ongoing financial challenges. (The Motley Fool)
The company faces intense competition from other gene-editing firms, such as Editas Medicine and Beam Therapeutics, which are developing similar therapies for sickle cell disease and beta-thalassemia, potentially impacting CRISPR's market share. (Nasdaq)
CRISPR Therapeutics' stock has experienced volatility, with a 34% decline over the past year, reflecting investor concerns over commercialization challenges and financial sustainability. (Nasdaq)
Data summarised monthly by Lightyear AI. Last updated on 7 Jul 2025.

CRISPR Financial Performance

Revenues and expenses
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
$37B
-39.75%
Net income
$45B
107.52%
Profit margin
37.65%
6.78%

CRISPR Earnings Performance

Company profitability
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
$3.69
$2.85
$2.45
$2.42
-
Expected
$3.55
$2.61
$2.05
$2.31
$3.94
Surprise
3.94%
9.20%
19.51%
4.63%
-
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
Real-time US market data is sourced from the IEX order book provided by Polygon. After-hours US market data is 15 minutes delayed and may differ significantly from the actual tradable price at market open.

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