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

Information source: Britannia Pharmaceuticals Ltd.
Information obtained from ClinicalTrials.gov on October 19, 2009
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Parkinson's Disease

Intervention: Apomorphine Nasal Powder (Drug)

Phase: Phase 2/Phase 3

Status: Not yet recruiting

Sponsored by: Britannia Pharmaceuticals Ltd.

Official(s) and/or principal investigator(s):
Richard Weiser, MB, MRCP, Principal Investigator, Affiliation: Swansea Hospital, Swansea, Wales

Summary

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

Clinical Details

Study design: Randomized, Double-Blind, Placebo Control, Parallel Assignment

Eligibility

Minimum age: 18 Years. Maximum age: 85 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- 1 year history of Parkinson's Disease; stable PD medications for 4 weeks; at least

one documented "off" period per day

Exclusion Criteria:

- hypersensitivity to apomorphine; participation in a clinical trial in the last 12

weeks; pregnant or lactating females

Locations and Contacts

Additional Information


Last updated: June 29, 2006

Page last updated: October 19, 2009

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