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A Phase III, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled Study Comparing the Efficacy and Safety of Gastric Retentive, Controlled Release Accordion PillTM Carbidopa/Levodopa (AP-CD/LD) to Immediate Release CD/LD in Fluctuating Parkinsons Disease Patients
Study Number
F16051
Summary
The purpose of this study is to determine whether the gastric retentive Accordion Pill™ Carbidopa/Levodopa (AP-CD/LD) is more effective than the commercially available immediate release Carbidopa/Levodopa in reducing motor fluctuations such as "off time" in advanced Parkinson''s Disease patients. 
Phase (?)
Phase III
Sponsor (?)
Contact

Pauline LeBlanc

Available at the following location(s)

Lebanon

View more details from ClinicalTrials.gov.

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