Cingulate’s 3Q25 results reflect continued progress toward transforming CTx-1301 into a commercial ADHD franchise. Recently the Company achieved several key milestones, including FDA acceptance of the CTx-1301 NDA with a May 31, 2026 PDUFA date, presentation of positive pediatric Phase 3 data demonstrating rapid onset and entire active-day symptom control, and execution of an exclusive commercial supply agreement with Bend Bio Sciences to secure U.S. manufacturing capacity ahead of launch. Together with its PTR platform and focused commercial strategy, Cingulate is positioning CTx-1301 to address unmet needs in the large U.S. ADHD market as it prepares for a potential 2026 launch, subject to FDA approval.