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Clinical trial

A Phase 3, Dose-Optimized, Randomized, Double-Blind, Placebo-Controlled, Single-Center, Parallel Efficacy and Safety Laboratory Classroom Study in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD) Using CTx-1301 (Dexmethylphenidate)

NCT05631626 is registered in ClinicalTrials.gov with Cingulate Therapeutics as lead sponsor.

NCT NCT05631626
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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 3, Dose-Optimized, Randomized, Double-Blind, Placebo-Controlled, Single-Center, Parallel Efficacy and Safety Laboratory Classroom Study in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD) Using CTx-1301 (Dexmethylphenidate)
Lead sponsor
Cingulate Therapeutics
Phase
Phase 3
Overall status
Completed
Start date
December 29, 2022
Completion date
June 13, 2023
Enrollment
26 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

adhd, adhd - combined type, attention deficit hyperactivity disorder, attention deficit hyperactivity disorder combined