CRISPR Therapeutics AG is a gene editing company, which engages in the development of transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. Its CRISPR/Cas9 platform is a gene editing technology that allows for precise, directed changes to genomic DNA. The firm offers a portfolio of therapeutic programs across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, and rare diseases. The company was founded by Rodger Novak, Emmanuelle Charpentier, Shaun Patrick Foy, Matthew Porteus, Daniel Anderson, Chad Cowan, and Craig Mellow on October 31, 2013 and is headquartered in Zug, Switzerland.
Stanford, Stanford, California, United States
UT Southwestern, Dallas, Texas, United States
Peter MacCallum Cancer Center, Melbourne, Victoria, Australia
Research Site 2, Saint Louis, Missouri, United States
Research Site 1, Nashville, Tennessee, United States
Research Site 3, Duarte, California, United States
Research Site, Nedlands, Western Australia, Australia
University of Alberta, Edmonton, Alberta, Canada
University of British Columbia, Vancouver, British Columbia, Canada
University of Alberta, Edmonton, Alberta, Canada
University of British Columbia, Vancouver, British Columbia, Canada
LMC Manna, Toronto, Ontario, Canada
Research Site 9, New York, New York, United States
Research Site 1, Houston, Texas, United States
Research Site 7, Toronto, Ontario, Canada
Research Site 2, Duarte, California, United States
Research Site 1, Melbourne, Victoria, Australia
Research Site 7, Amsterdam, North Holland, Netherlands
University of Pennsylvania, Philadelphia, Pennsylvania, United States
Sarah Cannon Research Institute, Nashville, Tennessee, United States
Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
University of Maryland, Baltimore, Maryland, United States
Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas, United States
Royal Prince Alfred Hospital, Sydney, New South Wales, Australia