Efficacy of Bifeprunox in Patients With Schizophrenia
Primary Purpose
Schizophrenia
Status
Terminated
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Bifeprunox
Placebo
Quetiapine
Sponsored by
About this trial
This is an interventional treatment trial for Schizophrenia focused on measuring Schizophrenia, Antipsychotic, Bifeprunox
Eligibility Criteria
Inclusion Criteria:
Main inclusion criteria
- The subject has a primary diagnosis of schizophrenia
- The subject experiences clinically significant symptoms
- The subject's medication remained stable for 8 weeks prior to screening
- The subject is currently in the post-acute maintenance phase of his/her disease
Exclusion Criteria:
Main exclusion criteria
- The subject is at significant risk of suicide
- The subject is treatment resistant
- The subject has experienced an acute exacerbation within 8 weeks prior screening
- The subject is unlikely to comply with the protocol
- The subject has a current diagnosis or a history of substance abuse
Sites / Locations
- IN008
- IN011
- IN009
- IN003
- IN006
- IN007
- IN002
- IN001
- IN010
- IN005
- ID002
- ID001
- ID003
- KR004
- KR008
- KR005
- KR006
- KR001
- KR007
- MY005
- MY001
- MY004
- MY003
- PH004
- PH001
- PH002
- PH003
- PH005
- PL005
- PL007
- PL002
- PL004
- PL003
- PL008
- PL006
- PL001
- UA008
- UA009
- UA006
- UA003
- UA004
- UA011
- UA005
- UA007
- UA010
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Placebo Comparator
Active Comparator
Arm Label
Bifeprunox
Placebo
Quetiapine
Arm Description
Outcomes
Primary Outcome Measures
The difference in change from baseline to the 12-week time point between bifeprunox and placebo using the Positive and Negative Syndrome Scale (PANSS).
Secondary Outcome Measures
The difference in PANSS score at the 12-month time point between bifeprunox and quetiapine. Also, responder rate, time to response/withdrawal, global clinical assessments (CGI), assessment of depressive symptoms (CDSS) and health economic assessments.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00704509
Brief Title
Efficacy of Bifeprunox in Patients With Schizophrenia
Official Title
A Multinational, Randomised, Double-Blind, Fixed-Dose, Bifeprunox Study Combining a 12-Week Placebo-Controlled, Quetiapine-Referenced Phase With a 12-Month Quetiapine-Controlled Phase in Patients With Schizophrenia
Study Type
Interventional
2. Study Status
Record Verification Date
September 2010
Overall Recruitment Status
Terminated
Why Stopped
Interim analysis showed inadequate efficacy of bifeprunox
Study Start Date
June 2008 (undefined)
Primary Completion Date
August 2009 (Actual)
Study Completion Date
November 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
H. Lundbeck A/S
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The primary purpose of the study is to evaluate the efficacy of bifeprunox in the maintenance phase of schizophrenia compared to placebo.
Detailed Description
Schizophrenia is a serious and disabling mental disorder that affects approximately 1% of the world's population. There are a number of antipsychotic drugs in use but none is ideal, in particular because their safety profile is complex and their effectiveness is limited. In particular, after having overcome acute exacerbations many patients continue to experience significant symptoms that prevent an adequate functioning. In the current study, patients suffering from schizophrenia and currently in a post-acute maintenance phase of the disease will be included. Non-treatment resistant patients will be included in the study, since they have partially responded to their current antipsychotic treatment but still have clinically significant symptoms and/or impairment of functioning in their daily life. The study is a 12-month study with an initial 12-week placebo-controlled, quetiapine-referenced phase. After this initial 12-week phase, the patients allocated to placebo will be switched to bifeprunox. In the final non-inferiority analysis of the 12-month data, the results from this study will be combined with the data from a similar study (11915A).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Schizophrenia, Antipsychotic, Bifeprunox
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
346 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Bifeprunox
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Quetiapine
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Bifeprunox
Other Intervention Name(s)
DU 127090
Intervention Description
20 mg daily, encapsulated tablets, orally, 12 months
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Encapsulated tablets, orally, 12 weeks
Intervention Type
Drug
Intervention Name(s)
Quetiapine
Other Intervention Name(s)
Seroquel
Intervention Description
600 mg daily, encapsulated tablets, orally, 12 months
Primary Outcome Measure Information:
Title
The difference in change from baseline to the 12-week time point between bifeprunox and placebo using the Positive and Negative Syndrome Scale (PANSS).
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
The difference in PANSS score at the 12-month time point between bifeprunox and quetiapine. Also, responder rate, time to response/withdrawal, global clinical assessments (CGI), assessment of depressive symptoms (CDSS) and health economic assessments.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Main inclusion criteria
The subject has a primary diagnosis of schizophrenia
The subject experiences clinically significant symptoms
The subject's medication remained stable for 8 weeks prior to screening
The subject is currently in the post-acute maintenance phase of his/her disease
Exclusion Criteria:
Main exclusion criteria
The subject is at significant risk of suicide
The subject is treatment resistant
The subject has experienced an acute exacerbation within 8 weeks prior screening
The subject is unlikely to comply with the protocol
The subject has a current diagnosis or a history of substance abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Email contact via H. Lundbeck A/S
Organizational Affiliation
LundbeckClinicalTrials@lundbeck.com
Official's Role
Study Director
Facility Information:
Facility Name
IN008
City
Ahmedabad
ZIP/Postal Code
380006
Country
India
Facility Name
IN011
City
Ahmedabad
ZIP/Postal Code
380013
Country
India
Facility Name
IN009
City
Aurangabad
ZIP/Postal Code
431005
Country
India
Facility Name
IN003
City
Bangalore
ZIP/Postal Code
560002
Country
India
Facility Name
IN006
City
Chennai
ZIP/Postal Code
600003
Country
India
Facility Name
IN007
City
Kanpur
ZIP/Postal Code
208005
Country
India
Facility Name
IN002
City
Lucknow
ZIP/Postal Code
226003
Country
India
Facility Name
IN001
City
Mangalore
ZIP/Postal Code
575018
Country
India
Facility Name
IN010
City
Varanasi
ZIP/Postal Code
221005
Country
India
Facility Name
IN005
City
Visakhapatnam
ZIP/Postal Code
530017
Country
India
Facility Name
ID002
City
Bangli
ZIP/Postal Code
80613
Country
Indonesia
Facility Name
ID001
City
Jakarta
ZIP/Postal Code
10430
Country
Indonesia
Facility Name
ID003
City
Kabupaten Bandung
ZIP/Postal Code
40551
Country
Indonesia
Facility Name
KR004
City
Busan
ZIP/Postal Code
614-735
Country
Korea, Republic of
Facility Name
KR008
City
Gyeongnam
ZIP/Postal Code
626-770
Country
Korea, Republic of
Facility Name
KR005
City
Pusan
ZIP/Postal Code
602-739
Country
Korea, Republic of
Facility Name
KR006
City
Seoul
ZIP/Postal Code
143-711
Country
Korea, Republic of
Facility Name
KR001
City
Seoul
ZIP/Postal Code
150-713
Country
Korea, Republic of
Facility Name
KR007
City
South Korea
ZIP/Postal Code
200-704
Country
Korea, Republic of
Facility Name
MY005
City
Johor Bahru
ZIP/Postal Code
Johor
Country
Malaysia
Facility Name
MY001
City
Kuala Lumpur
ZIP/Postal Code
50603
Country
Malaysia
Facility Name
MY004
City
Kuala Lumpur
ZIP/Postal Code
55100
Country
Malaysia
Facility Name
MY003
City
Perak
ZIP/Postal Code
31250
Country
Malaysia
Facility Name
PH004
City
Cebu City
ZIP/Postal Code
6000
Country
Philippines
Facility Name
PH001
City
Mandaluyong City
ZIP/Postal Code
1553
Country
Philippines
Facility Name
PH002
City
Manila
ZIP/Postal Code
1000
Country
Philippines
Facility Name
PH003
City
Pasig City
ZIP/Postal Code
1607
Country
Philippines
Facility Name
PH005
City
Quezon City
ZIP/Postal Code
0870
Country
Philippines
Facility Name
PL005
City
Choroszcz
ZIP/Postal Code
16-070
Country
Poland
Facility Name
PL007
City
Kutno
Country
Poland
Facility Name
PL002
City
Leszno
ZIP/Postal Code
64-100
Country
Poland
Facility Name
PL004
City
Lodz
ZIP/Postal Code
91-229
Country
Poland
Facility Name
PL003
City
Lublin
ZIP/Postal Code
20-109
Country
Poland
Facility Name
PL008
City
Skorzewo
ZIP/Postal Code
60-185
Country
Poland
Facility Name
PL006
City
Swicie n/Wisla
ZIP/Postal Code
86-100
Country
Poland
Facility Name
PL001
City
Torun
ZIP/Postal Code
87-100
Country
Poland
Facility Name
UA008
City
Dnipropetrovsk
ZIP/Postal Code
49005
Country
Ukraine
Facility Name
UA009
City
Donetsk
ZIP/Postal Code
83037
Country
Ukraine
Facility Name
UA006
City
Kharkiv
ZIP/Postal Code
61068
Country
Ukraine
Facility Name
UA003
City
Kyiv
ZIP/Postal Code
04080
Country
Ukraine
Facility Name
UA004
City
Lviv
ZIP/Postal Code
79021
Country
Ukraine
Facility Name
UA011
City
Odessa
ZIP/Postal Code
65006
Country
Ukraine
Facility Name
UA005
City
Poltava
ZIP/Postal Code
36024
Country
Ukraine
Facility Name
UA007
City
Stepanovka, Kherson
ZIP/Postal Code
73488
Country
Ukraine
Facility Name
UA010
City
Vinnitsa
ZIP/Postal Code
21018
Country
Ukraine
12. IPD Sharing Statement
Citations:
PubMed Identifier
32840872
Citation
Ceraso A, Lin JJ, Schneider-Thoma J, Siafis S, Tardy M, Komossa K, Heres S, Kissling W, Davis JM, Leucht S. Maintenance treatment with antipsychotic drugs for schizophrenia. Cochrane Database Syst Rev. 2020 Aug 11;8(8):CD008016. doi: 10.1002/14651858.CD008016.pub3.
Results Reference
derived
Learn more about this trial
Efficacy of Bifeprunox in Patients With Schizophrenia
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