Apomorphine Nasal Powder in the Treatment of Parkinson's Disease "Off" Periods.

NCT00346827 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2019-07-10

No results posted yet for this study

Summary

To determine the safety and tolerability of repeated dosing with Apomorphine Nasal Powder in subjects with Parkinson's Disease.

Conditions

Interventions

DRUG

Apomorphine Nasal Powder

Sponsors & Collaborators

  • Britannia Pharmaceuticals Ltd.

    lead INDUSTRY

Principal Investigators

  • Richard Weiser, MB, MRCP · Swansea Hospital, Swansea, Wales

Study Design

Purpose
TREATMENT
Masking
DOUBLE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-07-31
Primary Completion
2007-08-31
Completion
2007-08-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00346827 on ClinicalTrials.gov