A CRISPR treatment seems to have been effective for a baby’s devastating disease, but it is not clear whether such bespoke ...

One of the most commonly used gene-delivery methods relies on engineered viruses to insert stretches of genetic material into ...

The CRISPR-Cas9 patent landscape remains complex and unsettled. The Federal Circuit’s latest decision in University of California v.

CRISPR Therapeutics benefits from Casgevy’s approval and a deep pipeline, despite early rollout hurdles and cost challenges.

An infant in Philadelphia has been successfully treated with a customized Crispr gene-editing therapy for a rare and deadly disease, doctors reported Thursday—a breakthrough in the futuristic ...

When CRISPR was first introduced as a gene-editing tool in 2012, the world was in awe of all the possibilities it held — eventually earning its discoverers the Nobel Prize in Chemistry in 2020. Now, ...

They used CRISPR, the gene editing tool that won its inventors the Nobel Prize in 2020. Instead of cutting the DNA strand like the first CRISPR approaches, doctors employed a technique that flips ...

NEW ORLEANS — Greetings from ASGCT, where the gene therapy field had some great ... the unique misspelling in his DNA. The custom CRISPR treatment, built for just a single infant named KJ ...