Status: Planned
First registered on:
07/04/2017
Last updated on:
07/04/2017
1. Study identification
EU PAS Register NumberEUPAS18536
Official titleCharacterising the safety profile of lurasidone in clinical practice: A drug utilisatio and safety study using a United Kingdom primary care database
Study title acronymNone
Study typeObservational study
Brief description of the studyThe study will describe drug utilization patters and characterize the safety profile of lurasidone compared to other second generation antipsychotics in a real world UK primary healthcare setting
Was this study requested by a regulator?Yes: EMA
Is the study required by a Risk Management Plan (RMP)?
EU RMP category 3 (required)
Regulatory procedure number (RMP Category 1 and 2 studies only)
Other study registration identification numbers and URLs as applicable
2. Research centres and Investigator details
Coordinating study entity
Centre to which the investigator belongsOXON
Department/Research group
Organisation/affiliationOxon Epidemiology Ltd.
Details of (Primary) lead investigator
Title Dr
Last name Qizilbash MBChB MRCP(UK) BSc MSc DPhil(Oxon.)
First name Nawab
Is this study being carried out with the collaboration of a research network?
No
Other centres where this study is being conducted
Not applicable (single centre)
Countries in which this study is being conducted
National study
United Kingdom
3. Study timelines: initial administrative steps, progress reports and final report
PlannedActual
Date when funding contract was signed14/01/2014
Start date of data collection01/06/2017
Start date of data analysis
Date of interim report, if expected
Date of final study report01/12/2021
4. Sources of funding
Please provide estimates of the percentage of funding by source for this study
Names(s)Approximate % funding
Pharmaceutical companiesSunovion Pharmaceuticals Europe Ltd100
Charities
Government body
Research councils
EU funding scheme
5. Contact details for enquiries
Scientific Enquiries
Title Mr
Last name Clarke
First name Quentin
Address line 1Sunovion Pharmaceuticals Europe Ltd
Address line 2Southside
Address line 397-105 Victoria Street
CityLondon
PostcodeSW1E6QT
CountryUnited Kingdom
Phone number (incl. country code)44-0207-8212840
Alternative phone number
Fax number (incl. country code)
Public Enquiries
Title Mr
Last name Clarke
First name Quentin
Address line 1Sunovion Pharmaceuticals Europe Ltd
Address line 2Southside
Address line 397-105 Victoria Street
CityLondon
PostcodeSW1E6QT
CountryUnited Kingdom
Phone number (incl. country code)44-0207-8212840
Alternative phone number
Fax number (incl. country code)
6. Study drug(s) information
Single-Constituent (Substance INN)LURASIDONE
7. Medical conditions to be studied
Medical condition(s)Yes
Schizophrenia
8. Population under study
Age
Children (2 - 11 years)
Adolescents (12 - 17 years)
Adults (18 - 44 years)
Adults (45 - 64 years)
Adults (65 - 74 years)
Adults (75 years and over)
Sex
Male
Female
Other population
Renal impaired
Hepatic impaired
Pregnant women
9. Number of subjects
Estimated total number of subjects6611
10. Source of data
Is this study being carried out with an established data source?No
Sources of data
Routine primary care electronic patient registry
11. Scope of the study
What is the scope of the study?
Risk assessment
Drug utilisation study
Primary scope : Drug utilisation study
12. Main objective(s)
What is the main objective of the study?
The overall aim of this research is to characterise the safety profile of lurasidone compared other second generation antipsychotics in clinical practice
Are there primary outcomes?No
Are there secondary outcomes?No
13. Study design
What is the design of the study?
Cross-sectional study
14. Follow-up of patients
Will patients be followed up?Not applicable/no follow-up
15. Data analysis plan
Please provide a brief summary of the analysis method
Drug Utilisation Study: Descriptive statistics, including means (SD) and medians (10th to 90th percentiles) for continuous variables, and numbers and percentages for categorical variables will be used to examine the following characteristics in new users of lurasidone compared with all other second generation antipsychotic drugs combined: demographics, comorbidities and comedications, pattern of onset, dose adjustment, and duration of therapy, prevalence of
a schizophrenia diagnosis, and prevalence of other relevant psychiatric indications in the absence of a schizophrenia diagnosis. Numbers of patients censored from the study by calendar year, and length of follow-up by year of therapy initiation will be reported.
PASS: Exposure propensity scores will be used to frequency match new users of lurasidone with new users of comparator second generation antipsychotics. Patients will also be matched on age and gender.
16. ENCePP seal
Are you requesting the ENCePP seal for this study?
No
17. Full protocol
Not submitted
18. Study Results
Not submitted
Please list the 5 most relevant publications using data from your study
ReferenceLink to web-publication
None
19. Other relevant documents
Conflict(s) of interest of
investigator(s)Not submitted
Composition of Steering Group and
ObserversNot submitted
Other documentsNot
submitted
Signed Code of
Conduct Checklist
Not submitted
Signed Code of Conduct Declaration
Not submitted
Signed Checklist for Study
Protocols
Not submitted
