Menu
Annual · values202520242023202220212020201920182017201620152014
Operating Cash Flow-345.01 M CHF-142.77 M CHF-260.38 M CHF-495.74 M CHF538.97 M CHF-238.37 M CHF56.68 M CHF-96.24 M CHF-70.09 M CHF-52.86 M CHF59.43 M CHF-4.79 M CHF
Depreciation & Amortization19.48 M CHF19.26 M CHF19.84 M CHF24.17 M CHF17.95 M CHF9.18 M CHF4.72 M CHF3.52 M CHF3.02 M CHF925000 CHF127000 CHF38000 CHF
Stock-Based Compensation72.50 M CHF86.57 M CHF81.03 M CHF97.95 M CHF102.39 M CHF66.02 M CHF44.06 M CHF34.98 M CHF18.87 M CHF10.84 M CHF3.68 M CHF695000 CHF
Capital Expenditures914000 CHF1.90 M CHF9.47 M CHF37.19 M CHF81.70 M CHF18.36 M CHF6.68 M CHF2.77 M CHF7.81 M CHF3.02 M CHF1.15 M CHF
Cash Flow from Investing-31.80 M CHF-280.48 M CHF374.65 M CHF-258.65 M CHF-1.04 B CHF-541.17 M CHF1.32 M CHF-2.77 M CHF-8.31 M CHF31.88 M CHF-1.15 M CHF
Cash Flow from Financing426.03 M CHF331.98 M CHF62.66 M CHF38.59 M CHF250.94 M CHF1.02 B CHF430.98 M CHF315.93 M CHF2.61 M CHF183.22 M CHF96.73 M CHF5.12 M CHF
Dividends Paid
Stock Buybacks57000 CHF
Free Cash Flow-345.93 M CHF-144.68 M CHF-269.85 M CHF-532.93 M CHF457.27 M CHF-256.72 M CHF49.99 M CHF-99.01 M CHF-77.91 M CHF-55.88 M CHF58.27 M CHF

CRISPR Therapeutics AG is a Swiss biotechnology company focused on gene editing-based medicines for serious diseases. The company develops therapies using its proprietary CRISPR/Cas9 platform, which enables precise changes to DNA and supports a portfolio of programs across hemoglobin disorders, oncology, regenerative medicine, rare diseases, and autoimmune-related research areas. Its current product set includes approved and investigational cell and gene therapies designed to address conditions with significant unmet medical needs, while its research pipeline spans both ex vivo and in vivo approaches. CRISPR Therapeutics AG also works with strategic partners in biotech and life sciences to advance development and commercialization activities. Headquartered in Zug, Switzerland, the company plays a notable role in the evolving market for gene editing, where its technologies are used to create targeted, next-generation therapeutic candidates.