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CRISPR Therapeutics AG

CRSP· NASDAQ
CHCH
$57.33+9.80%
2026-09-17

Financials

Valuation Metrics

CRISPR Therapeutics AG's Market Cap is $5.53B. At end of 2025 it was $4.72B. Ranked #1282 of 3,121 in US market (top 41%), #433 of 1,463 on NASDAQ (top 30%), #78 of 266 in Pharmaceuticals, Biotechnology & Life Sciences (top 29%) by Market Cap.

Investment Metrics(as of 2026-09-18)

MetricValue
Size
Market Cap$5.53B
Revenue$13M
Net Income$-451M
Total Assets$2.65B
Net Assets$1.75B
Employees393
Value
P/B3.17x
P/S412.85x
FCF Yield-8.69%
Profitability
ROE-25.83%
ROA-17.02%
Op. Margin-3971.53%
Revenue Growth-64.15%
Financial Health
Debt Ratio51.77%
Total Debt$784M
FCF$-481M
Cash$291M
Current Ratio17.85x
Performance
1Y Return-2.95%
1M Return8.22%
From 52W High-26.96%
1Y MDD-42.25%
Trading
Volume2,978,452 shares
Trading Value$168M
Per Share
EPS$-4.68
BPS$18.11

Company Info

CEO Samarth Kulkarni
Employees 393
HQ Zug, CH

CRISPR Therapeutics AG (CRSP) is a biotechnology firm dedicated to pioneering gene-based medicines for severe diseases. The company achieves this through its exclusive Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) technology, which enables precise and targeted alterations to an organism's genetic code. Its extensive pipeline includes therapeutic candidates spanning multiple medical areas, such as blood disorders (hemoglobinopathies), various cancers (oncology), regenerative medicine, and rare conditions. The company's flagship investigational therapy is CTX001, an ex vivo CRISPR gene-edited treatment. This therapy aims to benefit patients with transfusion-dependent beta-thalassemia or severe sickle cell disease by modifying their own hematopoietic stem cells to markedly boost the production of fetal hemoglobin within red blood cells. CRISPR Therapeutics is also advancing several other genetically engineered allogeneic (donor-sourced) CAR-T investigational therapies: CTX110, designed to combat cluster of differentiation 19-positive malignancies; CTX120, which targets B-cell maturation antigen for multiple myeloma that has relapsed or proven resistant to previous treatments; and CTX130, focused on Cluster of Differentiation 70 for a spectrum of solid tumors and blood cancers. Furthermore, the company is developing VCTX210, an immune-evasive, gene-edited stem cell-derived product candidate for treating type 1 diabetes. It is also pursuing various in vivo gene-editing initiatives aimed at addressing disorders affecting the liver, lungs, muscles, and central nervous system. The company has forged strategic alliances with significant partners, including Bayer Healthcare LLC, Vertex Pharmaceuticals Incorporated, ViaCyte, Inc., Nkarta, Inc., and Capsida Biotherapeutics. CRISPR Therapeutics AG was established in 2013 and maintains its headquarters in Zug, Switzerland.