CompletedNCT02943213
Chlorpromazine Absorption From a New Tablet Formulation
About this title
Read the official source — NCT02943213Medication studyAges 18–65South AfricaSchizophrenia
Understand this study
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.
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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CompletedThis badge reflects the study status reported by the registry. Check the registry for the latest information.
Bloemfontein
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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.
