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FDA approves 2 gene therapies for sickle cell

Regulators on Friday approved two gene therapies for sickle cell disease that doctors hope can cure the painful, inherited blood disorder that afflicts mostly Black people in the U.S. ....

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UK approves gene therapy for sickle cell anaemia. Why it offers hope for Indian patients

Gray underwent a clinical trial in 2017 for the drug Casgevy, which uses the innovative gene-editing tool CRISPR-Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats and associated protein 9). ....

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Louise Glück honed her poetic voice across a lifetime to speak to us from beyond the grave

A celebrated poet and Nobel laureate, Louise Glück wrote about mortality, broken families and human frailty with devastating wryness and quiet beauty. ....

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CRISPR Therapeutics Awaits FDA Word On Its First Gene-editing Based Medicine

CRISPR Therapeutics (CRSP), a gene editing company developing gene-based medicines for serious diseases, is scheduled to participate in a fireside chat at Citi's 18th Annual Biopharma Conference on September 6. ....

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