CRISPR Therapeutics (CRSP)
CRISPR Therapeutics (NASDAQ: CRSP)
Founded: 2013
Headquarters: Zug, Switzerland
Focus Area: Development of gene-based therapeutics using CRISPR/Cas9 gene-editing technology
🔬 Key Pipelines / Technologies
Pipeline | Indication | Clinical Stage | Notes |
---|---|---|---|
exa-cel | Sickle Cell Disease (SCD) and Transfusion-Dependent β-Thalassemia (TDT) | Approved | Co-developed with Vertex Pharmaceuticals |
CTX112 | CD19+ B-cell malignancies and autoimmune diseases | Phase 1/2 | Next-generation allogeneic CAR-T therapy |
CTX131 | CD70+ solid tumors and hematologic malignancies | Phase 1/2 | Next-generation allogeneic CAR-T therapy |
- Source: CRISPR Therapeutics Pipeline
📅 Recent Major Events
💰 Financial Information
Item | Value |
---|---|
Market Capitalization | ~$3.7 billion |
Cash Holdings | ~$1.9 billion |
Annual R&D Spending | ~$400 million |
Operating Loss (2024) | ~$300 million |
Number of Employees | ~407 |
Estimated Cash Runway | ~5 years |
Formula = (Current Assets – Current Liabilities) / Previous Year's Operating Loss
Source: CRISPR Therapeutics 2024 Annual Report
🚀 Upcoming Catalysts / Risk Factors
- Upcoming Milestones:
- Mid-2025: Broad data update for CTX112 in oncology and autoimmune indications
- 2025: Clinical data update expected for CTX131
- H1 2025: Initial clinical data readouts for new programs CTX310 and CTX320
- Risk Factors:
- Pipeline Risk: Potential failure or unexpected adverse events in clinical trials
- Regulatory Risk: Changes in global regulatory environment for gene-editing technologies
- Competitive Pressure: Intensifying competition in the gene therapy space
- Off-target Effects: Possibility of unintended gene edits inherent in CRISPR-based approaches
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Updated: 2025-03-22