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A Multiple-Dose Study of Sinemet® CR (Carbidopa/Levodopa) in Healthy Subjects

An Open Label, Multiple-Dose Study ot Determine the Plasma Levodopa Profiles of Sinemet® CR (Carbidopa/Levodopa) at 4 Daily Dose Levels in Healthy Subjects

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00460954
Enrollment
20
Registered
2007-04-17
Start date
2007-06-30
Completion date
2007-08-31
Last updated
2008-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson's Disease

Brief summary

The purpose of this clinical research study is to determine if different dosage regimens of Sinemet® CR (Carbidopa/levodopa) are dose proportional

Interventions

DRUGSinemet® controlled release (Carbidopa/levodopa)

Sponsors

Bristol-Myers Squibb
Lead SponsorINDUSTRY

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Key inclusion and

Exclusion criteria

for healthy volunteers will be used * Males and females aged 50-75

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026