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Stanford doctors develop first FDA-approved gene-editing treatment

The FDA recently approved Casgevy, a gene-editing medical treatment which uses CRISPR/Cas9 technology to treat sickle cell disease. Casgevy, which two Stanford faculty members contributed to via drug development and FDA approval, is the first gene-editing medical treatment to recieve FDA approval.

United statesJoseph wuJennifer doudnaEmmanuelle charpentierPaulo henrique orlandi mouraoMatthew porteusStanley qiStanford cardiovascular instituteDrug administrationStanford professorStanford medicineNobel prizeAssociate professorScientific founder

Best Related Work Hugo | File 770

Best Related Work Hugo | File 770
file770.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from file770.com Daily Mail and Mail on Sunday newspapers.

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Getting a Next-Generation Genome Editing Therapy for Sickle Cell Disease Back on Track

Getting a Next-Generation Genome Editing Therapy for Sickle Cell Disease Back on Track
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FDA Approves the First CRISPR Therapy for Sickle Cell Disease

FDA Approves the First CRISPR Therapy for Sickle Cell Disease
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A Sickle Sequel: Matthew Porteus Launches Kamau with Positive Nula-Cell Patient Zero Results

A Sickle Sequel: Matthew Porteus Launches Kamau with Positive Nula-Cell Patient Zero Results
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