Dr. Swee Lay Thein and Dr. Stuart Orkin won the $3 million Breakthrough Prize in Life Sciences for their work toward a ...
You might like the sound of this news. In a landmark move, the Food and Drug Administration on Thursday approved the first ...
Travis Smith was a very serious baby. Born completely unable to hear, his mother, Sierra, struggled to see his personality ...
A new gene therapy is giving people born deaf the chance to hear, often within just weeks. In a small but groundbreaking study, researchers delivered a working copy of a key hearing gene directly into ...
A new study has brought scientists one step further in the direction of developing a cure for a brutal group of rare brain disorders known as SYNGAP1-related disorders, or SRDs. Researchers were able ...
The idea behind intra-articular gene therapy for treating osteoarthritis (OA) is to deliver the gene-altering vector or cells directly to the precise site of the disease with a single injection — so ...
Forbes contributors publish independent expert analyses and insights. A patient in a late-stage gene editing trial for a rare heart condition died from fatal liver complications after receiving an ...
The US Food and Drug Administration on Thursday approved the first gene therapy for inherited hearing loss, a one-time ...
Married couple Jean Bennett and Albert Maguire developed Luxturna, which helped a patient see their child’s face for the first time ...
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Harvard couple wins $3M 'Oscar of science' for first gene therapy to reverse childhood blindness
A married couple of scientists has won the 2026 Breakthrough Prize in Life Sciences for creating the world's first gene ...
Three scientists have won the 2026 Breakthrough Prize for developing Luxturna — the world's first FDA-approved gene therapy ...
The breakthrough treatment, developed over 25 years, has already helped restore vision for some patients.
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