Gene editing has delivered remarkable results against sickle cell disease. Now researchers are working to make these ...

A handful of start-up firms are testing therapies that target specific epigenetic markers to treat everything from high ...

Casgevy also now indicated for transfusion-dependent beta thalassemia in children 2 years ...

The gene editing tool known as CRISPR-Cas9 is changing what's possible for treating a wide range of diseases caused by genetic mutations. But so far, attempts to use the technology to address ...

Researchers discovered the secret checkpoints that keep CRISPR precise, revealing how the tool shifts from inactive to active without misfiring. The insight could transform gene therapy, making ...

CRISPR Therapeutics wins FDA pediatric approval for Casgevy, boosting market potential and pipeline upside despite slow uptake. Click here to read more.

A handful of start-up firms are testing therapies that target specific epigenetic markers to treat everything from high ...

The company seems to be doing everything it's supposed to be doing; the stock just isn't responding.

The Gene Editing Therapeutics market, driven by advancements in CRISPR technology and precision medicine, presents opportunities in oncology, rare genetic disorders, and chronic diseases. Investment ...

The inventor of the groundbreaking Crispr gene-editing technology is skeptical about artificial intelligence replacing human ...

A major medical milestone took place in May 2025, when doctors at the Children’s Hospital of Philadelphia used CRISPR-based gene editing to treat a child with a rare genetic disorder. Unlike earlier ...

People living with hereditary angioedema, a rare genetic condition that triggers sudden, painful swelling of the face, throat ...