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SuspendedNCT05924594

Phase 3 Efficacy and Safety Laboratory Classroom Study in Pediatrics (6-12) With ADHD Using CTx-1301

Medication studyAges 6–12United States
The study in practice

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Who could participate?

Listed age limits: 6 years to 12 years.

Listed locations
Maitland and 2 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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What to know before participating

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Things to check before joining

Study start dateStarted: July 31, 2023
Recruitment status
Suspended
Enrollment listed in the registry
45
Sponsor
Cingulate Therapeutics
Sponsor type
Biotech company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 6 Years to 12 Years
Official registry ID
NCT05924594
Official title
Show the full official 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)

Recruitment & locations

Suspended

Maitland · Las Vegas · North Charleston

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Cingulate Therapeutics.

Does this study involve medication?

Yes. The study involves medication, including CTx-1301 - Dexmethylphenidate 6.25mg, CTx-1301 - Dexmethylphenidate 12.5mg, CTx-1301 - Dexmethylphenidate 18.75mg, CTx-1301 - Dexmethylphenidate 25.0mg, CTx-1301 - Dexmethylphenidate 31.25mg, CTx-1301 - Dexmethylphenidate 37.5mg and Placebo.

Who can participate?

Listed age limits: 6 years to 12 years.

Is this study still recruiting?

The registry lists this study as suspended.

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