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CRISPR Therapeutics CRSP

Pioneer of CRISPR gene-editing therapies.

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What it does

Develops treatments that fix or switch off genes. With Vertex, it created Casgevy, the first approved CRISPR therapy, for sickle cell disease and beta thalassemia.

Ticker
NASDAQ:CRSP
Headquarters
Zug, Suíça
Founded
2013
Evidence Radar

✓ Evidence

  • Casgevy approved in the US, UK and EU (2023–2024).

◷ Promises

  • Gene editing for cardiovascular disease and cancer.

⚠ What could go wrong

  • Slow commercial uptake of expensive, complex therapies.
  • Uncertain clinical results.
  • Cash burn.

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