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Cingulate Reports Safety Results from Final Phase 3 Trials for Lead ADHD Asset CTx-1301: On Track to File for FDA Approval Mid-2025

Provided By GlobeNewswire

Last update: Mar 4, 2025

Results Have Been Submitted Ahead of In-Person Meeting with FDA Set for April 2

CTx-1301 is the First, True, Once-Daily Stimulant Medication to Treat ADHD Over the Entire Active Day

Read more at globenewswire.com

CINGULATE INC

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