CRISPR Therapeutics

CRISPR Therapeutics

Biotechnology
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.

$4.8B

Market Cap • 10/16/2026

2013

(13 years)

Founded

2016

(10 years ago)

IPO

NASDAQ

Listing Exchange

Flag of Switzerland

Switzerland

Country

Valuation

P/B

2,7

P/S

355,6

P/EBITDA

—

P/OCF

—

P/FCF

—

P/E

—

BVPS

18,1

EPS

—

Market Cap

Market Cap

4,8B

EV

3,2B

EV/Revenue

237,6

EV/EBITDA

-6,2

EV/EBIT

-6

Payout

Dividend Per Share

0

Dividend Yield

0%

Buyback Yield

-9%

Total Yield

-9%

Payout

0%

Retained Earnings

-2,2B

Profitability

Gross Margin

—

EBITDA Margin

—

EBIT Margin

—

Net Margin

—

D&A/EBITDA

0%

R&D/Revenue

2095,5%

Capex/Revenue

13%

Capex/D&A

9,3%

Capex/OCF

-0,5%

SBC/OCF

—

% PPE

8,8%

% Goodwill

0%

ROE

—

ROIC

—

Growth

CAGR Revenue 5Y

-56,9%

Leverage

N.D./EBITDA

3,1

Debt/Equity

0%

Current Ratio

17,8

Quick Ratio

17,8

Interest Coverage

—

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