U.S. poised to approve first gene-editing treatment in breakthrough for sickle cell patients

The U.S. Food and Drug Administration is expected to approve exa-cel for sickle cell disease in what would become the first marketed medicine to use CRISPR.

Previous post Biden administration asserts power to seize drug patents in move to slash high prices
Next post PGA Tour star Jon Rahm could be gearing up to join Saudi-backed LIV Golf