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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00627640




Registration number
NCT00627640
Ethics application status
Date submitted
13/02/2008
Date registered
3/03/2008
Date last updated
29/03/2013

Titles & IDs
Public title
Safinamide in Idiopathic Parkinson's Disease (IPD) With Motor Fluctuations, as add-on to Levodopa
Scientific title
A Phase III, Double-blind, Placebo-controlled, Randomised Trial to Determine the Efficacy and Safety of a Dose Range of 50 to 100 mg/Day of Safinamide, as add-on Therapy, in Subjects With Idiopathic Parkinson's Disease With Motor Fluctuations, Treated With a Stable Dose of Levodopa and Who May be Receiving Concomitant Treatment With Stable Doses of a Dopamine Agonist, an Anticholinergic and/or Amantadine
Secondary ID [1] 0 0
IND: 63,901
Secondary ID [2] 0 0
27919
Universal Trial Number (UTN)
Trial acronym
SETTLE
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Idiopathic Parkinson's Disease 0 0
Condition category
Condition code
Neurological 0 0 0 0
Parkinson's disease

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Safinimide 50-100 mg/day
Treatment: Drugs - Matching Placebo

Experimental: 1 - 1 active (50 - 100 mg/day)

Placebo comparator: 2 -


Treatment: Drugs: Safinimide 50-100 mg/day
Safinamide, (S)-(+)-2-\[4-(3-fluorobenzyloxy) benzylamino\] propanamide methanesulfonate, is an a-aminoamide derivative

Treatment: Drugs: Matching Placebo
Matching Placebo
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Evaluate the change from baseline to W24 in daily "on" time ("on" time without dyskinesia plus "on" time with minor dyskinesia)
Timepoint [1] 0 0
24 weeks
Secondary outcome [1] 0 0
Evaluate the changes from baseline to W24 in Activities of Daily Living, cognition, dyskinesias, change in global clinical status, motor symptoms, motor fluctuations, change in levopoda dose and Health Related Quality of life
Timepoint [1] 0 0
24 weeks

Eligibility
Key inclusion criteria
Male and female between the ages of 30 to 80 years with diagnosis of idiopathic Parkinson's Disease of more than 5 years duration, with a Hoehn and Yahr stage of I-IV during an "off" phase.

Be levodopa-responsive and have been receiving treatment with a stable dose of levodopa for at least 4 weeks.

Have motor fluctuations, with >1.5 hours "off" time during the day. Be able to maintain an accurate and complete diary (18-hour)
Minimum age
30 Years
Maximum age
80 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Patients with medical conditions and/or taking concomitant medications that would have put them at risk, interfered with the study evaluations, or made them unable to complete the requirements of the study;.

Be in a late stage of Parkinson's Disease, and experiencing severe, disabling peak-dose or biphasic dyskinesia and/or unpredictable or widely swinging fluctuations in their symptoms.

Current diagnosis of substance abuse or history of alcohol or drug abuse in the past 3 months.

Have received treatment with safinamide previously. History of, or current depression psychosis (e.g. schizophrenia or psychotic depression) Evidence of dementia or cognitive dysfunction. History of allergic response to anticonvulsants, levodopa, or other anti-Parkinsonian agents.

Hypersensitivity or contraindications to MAO-B inhibitors. Ophthalmologic history including any of the following conditions: albino subjects, family history of hereditary retinal disease, progressive and/or severe diminution of visual acuity (i.e., 20/70), retinitis pigmentosa, retinal pigmentation due to any cause, any active retinopathy or ocular inflammation (uveitis), or diabetic retinopathy.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/02/2009
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/03/2012
Sample size
Target
Accrual to date
Final
549
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Concord Repatriation General Hospital - Concord
Recruitment hospital [2] 0 0
Central Coast Neuroscience Research - East Gosford
Recruitment postcode(s) [1] 0 0
- Concord
Recruitment postcode(s) [2] 0 0
- East Gosford
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Alabama
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United States of America
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Arizona
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United States of America
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California
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United States of America
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Connecticut
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Florida
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Georgia
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Illinois
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Kansas
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United States of America
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Maryland
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Massachusetts
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Michigan
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New York
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North Carolina
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Pennsylvania
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Tennessee
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Texas
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Austria
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Graz
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Austria
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Innsbruck
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Belgium
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Brussels
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Belgium
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Edegem
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Belgium
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Hasselt
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Belgium
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Hoboken
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Belgium
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Roeselare
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Belgium
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Wilrijk
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Canada
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Nova Scotia
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Ontario
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Quebec
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Canada
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Halifax
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Kingston
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Estonia
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Tartu
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France
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Clermont Ferrand
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France
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Miletrie Poitiers
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France
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Nantes Cedex
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France
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Nimes Cedex
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France
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Pavillon Riser Toulouse
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Germany
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Beelitz-Heilstaetten
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Germany
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Berlin
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Germany
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Goettingen
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Germany
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Leipzig
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Germany
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Marburg
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Germany
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Mittweida
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Germany
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Muenchen
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Germany
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Tubingen
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Germany
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Ulm
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Germany
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Wiesbaden
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Hungary
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Budapest
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Debrecen
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Miskolc
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Móricz
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Peterfy Sandor
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Sopron
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India
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Andh Prad
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Karna
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Mangalore
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Nagpur
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Vellore
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Israel
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Zefat
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Korea, Republic of
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Seoul
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Malaysia
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Kuala Lumpur
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Malaysia
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Pinang
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Netherlands
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Hertogenbosch
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New Zealand
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Aucklan
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New Zealand
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Christchurch
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New Zealand
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Hamilton
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Slovakia
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Banska Bystrica
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Slovakia
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Bratislava
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Levoca
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Slovak Republic
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Spain
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Madrid
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Spain
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Malaga
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Spain
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San Sebastian
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Switzerland
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Bern
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Switzerland
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Geneve
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Chang Hua
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Kaohsiung
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Taipei
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Thailand
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Bangkok
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Thailand
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Lampang
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Thailand
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Ubonratchathani
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United Kingdom
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Blackpool
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United Kingdom
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Cambridge
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Glasgow
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London
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United Kingdom
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Newcastle Upon Tyne

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Newron Pharmaceuticals SPA
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Algirdas Kakarieka, MD
Address 0 0
Merck Serono S.A., Geneva
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT00627640