CTx-1301 Comparative Bioavailability Study

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

45

Participants

Timeline

Start Date

December 6, 2019

Primary Completion Date

March 6, 2020

Study Completion Date

March 6, 2020

Conditions
ADHD
Interventions
DRUG

Dexmethylphenidate 5 Mg Oral Capsule, Extended Release

Reference listed drug (RLD) for comparative BA evaluation

DRUG

Dexmethylphenidate 6.25 mg Tablet

Experimental drug for comparative BA evaluation

DRUG

Dexmethylphenidate 40 Mg Oral Capsule, Extended Release

Reference listed drug (RLD) for comparative BA evaluation

DRUG

Dexmethylphenidate 50 mg Tablet

Experimental drug for comparative BA evaluation

Trial Locations (1)

66212

Vince & Associates, Overland Park

Sponsors
All Listed Sponsors
lead

Cingulate Therapeutics

INDUSTRY

NCT04138498 - CTx-1301 Comparative Bioavailability Study | Biotech Hunter | Biotech Hunter