Gene therapy developer CRISPR Therapeutics AG (CRSP) is navigating some regulatory and commercial dynamics. Its flagship gene therapy product for treating sickle cell disease, Casgevy, faces market hurdles. However, recent political developments, including both at the White House and the Food and Drug Administration (FDA), have paved the way for CRISPR to secure payment for Casgevy and advance new treatments. As a result, I am bullish on CRISPR’s prospects in the short term, although some doubts