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CompletedNCT00796029

A Study of Plasma Concentrations, Metabolism and Excretion of 14C-paliperidone After a Single Oral Dose

Medication studyAges 40–60Schizophrenia
The study in practice

Understand this study

Who was this study for?

Listed age limits: 40 years to 60 years.

Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
Study clarity

Study information

Study start dateJuly 2003
Recruitment status
Completed
Enrollment listed in the registry
5
Sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
Locations
Not clearly listed
Age range
From 40 Years to 60 Years
Official registry ID
NCT00796029
Official title
Show the full official title

Plasma Concentrations, Metabolism and Excretion of 14C-paliperidone After a Single Oral Dose in Healthy Male Subjects

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Recruitment & locations

Completed

Locations not listed

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Johnson & Johnson Pharmaceutical Research & Development, L.L.C., a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including 14C-paliperidone.

Who was this study for?

Listed age limits: 40 years to 60 years.

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