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Sustained Release Oral Formulation for Treatment of Parkinson's Disease

Sustained Release Oral Formulation for Treatment of Parkinson's Disease

Recruiting
18-65 years
All
Phase N/A
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Overview

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.

Eligibility

Inclusion Criteria:

  • Normal healthy
  • Are 18-65 years of age
  • Are not currently taking medications regularly
  • Able to fast 6 hours (water allowed)

Exclusion Criteria:

  • Pregnancy
  • Inability to fast

Study details
    Healthy Volunteers

NCT05471609

University of Minnesota

21 July 2025

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