One company leads in gene-editing approvals, while the other targets surging demand in metabolic treatments. Here’s how their ...
One year after receiving three doses of a custom-built CRISPR base-editing therapy at Children’s Hospital of Philadelphia, ...
A handful of start-up firms are testing therapies that target specific epigenetic markers to treat everything from high ...
In a study published in Science Translational Medicine, a team of researchers led by Dr. Wang Yu from the Shenzhen Institutes ...
In late June 2026, CRISPR Therapeutics AG was added to several Russell growth indexes, including the Russell 2000 Growth, ...
Gene editing has delivered remarkable results against sickle cell disease. Now researchers are working to make these ...
The opportunity is enormous, but uncertainty remains.
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.
Casgevy sickle cell gene therapy is now FDA-approved for children as young as two, opening access for 5,500 more U.S. kids.
A team of researchers led by Professor Akitsu Hotta (Department of Clinical Application) developed a comprehensive framework ...
From gene-editing breakthroughs to blockbuster cystic fibrosis drugs, these two industry leaders present sharply contrasting ...