Clinical trial
A Phase 3, Dose-Optimized, Double-Blind, Randomized, Placebo-Controlled, Parallel Efficacy and Safety Laboratory Classroom Study in Children (6-12) With Attention-Deficit/Hyperactivity Disorder (ADHD) Using CTx-1301 (Dexmethylphenidate)
NCT05924594 is registered in ClinicalTrials.gov with Cingulate Therapeutics as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 3, Dose-Optimized, Double-Blind, Randomized, Placebo-Controlled, Parallel Efficacy and Safety Laboratory Classroom Study in Children (6-12) With Attention-Deficit/Hyperactivity Disorder (ADHD) Using CTx-1301 (Dexmethylphenidate)
- Lead sponsor
- Cingulate Therapeutics
- Phase
- Phase 3
- Overall status
- Suspended
- Start date
- July 31, 2023
- Completion date
- February 28, 2027
- Enrollment
- 45 (actual)
- Sites
- 3
Conditions
As the registry lists them; a condition with its own page is linked.
adhd, adhd - combined type, attention deficit disorder with hyperactivity, attention deficit hyper activity, attention deficit hyperactivity disorder, attention deficit hyperactivity disorder combined, attention-deficit hyperactivity