Controlled Study of ONO-2506PO in Patients With Parkinson's Disease in Japan

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

165 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-01-31

Brief Summary

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The purpose of this study is to evaluate the efficacy and safety of ONO-2506PO in patients with Parkinson's Disease

Detailed Description

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Conditions

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Parkinson's Disease

Keywords

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ONO-2506PO, Parkinson's disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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ONO-2506PO

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Diagnosis of Parkinson's disease
2. Stage 2 - Stage 4 of revised Hoehn \& Yahr severity score
3. Taking L-dopa/DCI without changing dose and regimen
4. Having motor complication

Exclusion Criteria

1. Previous participation in ONO-2506PO or ONO-2506 protocol
2. Previous brain surgery for Parkinson's disease
3. Presence or history of serious cardiac disease

Minimum Eligible Age

20 Years

Maximum Eligible Age

79 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Project Leader, Development Planning

Role: STUDY_DIRECTOR

Ono Pharmaceutical Co. Ltd

Other Identifiers

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ONO-2506PO-03

Identifier Type: -

Identifier Source: org_study_id