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Gene Therapy

Bayer hands control of Casebia to Crispr Therapeutics

by Ryan Cross
October 26, 2019 | A version of this story appeared in Volume 97, Issue 42
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Bayer and Crispr Therapeutics teamed up in December 2015 to launch Casebia Therapeutics to develop gene-editing therapies for blood, eye, and heart diseases. Bayer pledged $300 million to the start-up, and Crispr pitched in $35 million. Bayer now plans to give Crispr full control of Casebia, although it still has rights to opt into two of the firm’s programs. Casebia is developing gene-editing therapies for hemophilia, multiple genetic forms of blindness, and a rare autoimmune disorder.

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