The US FDA must approve a second distinct CRISPR/Cas9-based gene therapy (beyond Casgevy for sickle cell/beta-thalassemia) for any indication before December 31, 2026. Based on FDA approval announcements.
Sign in to make predictions, track your accuracy, and compete on the leaderboard.
Sign in to predictNo comments yet. Be the first to share your reasoning.
Sign in to join the discussion