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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy, safety and tolerability of PF-06649751 in Parkinson's disease patients at early stage of the disease.


Clinical Trial Description

The B7601011 study has a randomized, double-blind, placebo-controlled parallel group design. Approximately 88 subjects will be randomized to 2 treatment groups. Each subject will participate in the study for approximately 23 weeks including a 30 day screening period, 15 week double blind treatment period, and an approximately 28 day follow-up period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02847650
Study type Interventional
Source Pfizer
Contact
Status Terminated
Phase Phase 2
Start date October 17, 2016
Completion date January 29, 2018

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