CRISPR Therapeutics
CRISPR Therapeutics is a biotechnology company that specializes in the development of transformative gene-based medicines using its proprietary CRISPR/Cas9 platform. CRISPR/Cas9 is a revolutionary gene-editing technology that allows for precise, directed changes to genomic DNA.
History[edit | edit source]
CRISPR Therapeutics was founded in 2013 by Emmanuelle Charpentier, one of the pioneers of the CRISPR/Cas9 technology. The company is headquartered in Zug, Switzerland, with operations in the United States.
Technology[edit | edit source]
CRISPR Therapeutics utilizes the CRISPR/Cas9 system, a technology that allows scientists to edit genes within organisms. The technology is considered a significant breakthrough in the field of genetic engineering, as it allows for precise editing of the genetic code.
Therapies[edit | edit source]
CRISPR Therapeutics is developing therapies across a broad range of diseases, including cancer, diabetes, and rare genetic disorders. The company's lead product candidate, CTX001, is being developed for the treatment of sickle cell disease and beta-thalassemia.
Clinical Trials[edit | edit source]
CRISPR Therapeutics has several therapies in clinical trials. The most advanced of these is CTX001, which is in Phase 1/2 clinical trials for the treatment of sickle cell disease and beta-thalassemia.
Partnerships[edit | edit source]
CRISPR Therapeutics has established partnerships with several pharmaceutical and biotechnology companies to accelerate the development of its therapies. These include collaborations with Vertex Pharmaceuticals and Bayer AG.
See Also[edit | edit source]
References[edit | edit source]
External Links[edit | edit source]
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