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CompletedNCT02943213

Chlorpromazine Absorption From a New Tablet Formulation

About this titleRead the official source — NCT02943213
Medication studyAges 18–65South AfricaSchizophrenia
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Who was this study for?

Listed age limits: 18 years to 65 years.

Listed locations
BloemfonteinSee all locations and recruitment
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.

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Study clarity

Study information

Study start dateNovember 2016
Recruitment status
Completed
Enrollment listed in the registry
20
Sponsor
Cycle Pharmaceuticals Ltd.
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
Locations
South Africa
Age range
From 18 Years to 65 Years
Official registry ID
NCT02943213
Official title
Show the full official title

A Single Center, Single Dose, Open-Label, Two-Period Replicate Pilot Study to Investigate Intra-subject Variability in the Bioavailability of a Formulation Containing Chlorpromazine Hydrochloride (25 mg Sugar Coated Tablets) in at Least 16 Healthy Males and Females Under Fasting Conditions

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Recruitment & locations

Completed

Bloemfontein

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Cycle Pharmaceuticals Ltd.

Did this study involve medication?

Yes. The study involved medication, including Chlorpromazine Hydrochloride.

Who was this study for?

Listed age limits: 18 years to 65 years.

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