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RECRUITING
NCT05471609
EARLY_PHASE1

Sustained Release Oral Formulation for Treatment of Parkinson's Disease

Sponsor: University of Minnesota

View on ClinicalTrials.gov

Summary

Achieving sustained blood levels of carbidopa/levodopa has been a challenge in the treatment of PD and although levodopa remains the most commonly used drug, motor fluctuations remain a major disability especially in advanced Parkinson's disease. The aim of this study is to determine the efficacy of a novel oral carbidopa-levodopa formulation in achieving a sustained blood level of levodopa and carbidopa in normal volunteers.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

6

Start Date

2025-06-12

Completion Date

2026-06-16

Last Updated

2025-07-10

Healthy Volunteers

Yes

Interventions

DRUG

levodopa/carbidopa oral formulation A

Outer sachet 100mg CD/100mg LD and inner sachet 0mg CD /300mg LD

DRUG

levodopa/carbidopa oral formulation B

Outer sachet 100mg CD/0mg LD and inner sachet 0mg CD /400mg LD

Locations (1)

University of Minnesota

Minneapolis, Minnesota, United States