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Cingulate presents Phase 3 results for CTx-1301, met primary endpoint

Cingulate (CING) announced that the positive Phase 3 results from its pivotal trial of CTx-1301 in pediatric ADHD, were recently presented by Ann Childress, M.D., at the AACAP Annual Meeting in Chicago. CTx-1301 met its primary endpoint, demonstrating dose-dependent improvements on the ADHD ratings scale 5, and Clinical Global Impression-Severity scales, and demonstrated the ability to deliver symptom relief with the convenience of once-daily dosing.

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