Multiple Ascending Dose Study of PRX002 in Patients With Parkinson's Disease

A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study of PRX002 Administered By Intravenous Infusion in Patients With Parkinson's Disease

Recruitment Information:

Seeking volunteers with following diagnosis: PD Study Type: Interventional
Eligible Ages: 40 - 80 Status: Completed
Time Since Diagnosis: Less than 60 years Study Focus:

Study Purpose:

This multiple ascending dose study is to determine safety, tolerability, pharmacokinetics and immunogenicity of PRX002 in approximately 60 patients with Parkinson's disease.

More Details

Phase: Phase 1 Lead Sponsor: Prothena Biosciences Limited
Trial ID: 003853 Sponsor Type: Industry
Primary Country: United States Additional Collaborators or Sponsors: Hoffmann-La Roche
Estimated Enrollment: 64 Study Start Date: June 2014
Estimated Study Completion Date: October 2016 Source: ClinicalTrials.gov
Study Website:
This is a FDA Regulated Trial

More Inclusion & Exclusion Criteria

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