Market OpportunityConsidering the ongoing stimulant shortages, especially for generic stimulant products, and that CTx-1301 only requires one dose, daily, the commercial opportunity for Cingulate is attractive.
Product EfficacyCTx-1301 demonstrated a potential best-in-class onset and duration for ADHD, making it a competitive differentiator amidst ongoing stimulant shortages.
Regulatory ProgressCingulate has completed its final FDA-required clinical program for CTx-1301, which is a significant step towards FDA approval for the treatment of ADHD.