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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00346827
Other study ID # 20102D05
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date July 2006
Est. completion date August 2007

Study information

Verified date July 2019
Source Britannia Pharmaceuticals Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date August 2007
Est. primary completion date August 2007
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Apomorphine Nasal Powder


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Britannia Pharmaceuticals Ltd.
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