Over a Decade of Innovation

We are pioneering a new era of medicines
Transforming the lives of patients living with serious diseases


Across a number of disease areas

1

Approved
Therapy

5

Clinical
Programs

10

Preclinical
Programs

First-ever approved crispr-based therapy

CASGEVY™ (Exagamglogene Autotemcel), a CRISPR/Cas9 Gene-Edited Therapy Arising Out of Our Collaboration with Vertex Pharmaceuticals Incorporated, Is Approved in Some Countries for Certain Eligible Patients with Sickle Cell Disease or Transfusion-Dependent Beta Thalassemia.

Committed to patients

Developing gene-based medicines with the potential to transform the lives of people with serious diseases

Rapidly translating a revolutionary technology into therapies

Innovation that matters

Rapidly translating a revolutionary technology into therapies

Learn more about gene editing

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