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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00707980




Registration number
NCT00707980
Ethics application status
Date submitted
27/06/2008
Date registered
2/07/2008
Date last updated
13/12/2013

Titles & IDs
Public title
Safety and Tolerability of Vortioxetine (Lu AA21004) in Adults With Major Depressive Disorder
Scientific title
A Long-Term, Open-Label, Flexible-Dose, Extension Study Evaluating the Safety and Tolerability of Lu AA21004 in Subjects With Major Depressive Disorder
Secondary ID [1] 0 0
2008-001581-91
Secondary ID [2] 0 0
LuAA21004_301
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Major Depressive Disorder 0 0
Condition category
Condition code
Mental Health 0 0 0 0
Depression

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Vortioxetine

Experimental: Vortioxetine - Vortioxetine 2.5 mg, 5 mg or 10 mg, encapsulated tablets, orally, once daily for up to 52 weeks. For the first week of treatment all participants received 5 mg/day vortioxetine, thereafter, the dose could be increased to 10 mg/day or decreased to 2.5 mg/day, based on participant's response and tolerability as judged by the investigator.


Treatment: Drugs: Vortioxetine
Encapsulated vortioxetine immediate-release tablets
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Physical Examination Findings
Timepoint [1] 0 0
Baseline and Week 52
Primary outcome [2] 0 0
Number of Participants With Potentially Clinically Significant Laboratory Evaluation Findings
Timepoint [2] 0 0
Weeks 4, 8, 12, 20, 28, 36, 44 and 52
Primary outcome [3] 0 0
Number of Participants With Potentially Clinically Significant Electrocardiogram (ECG) Findings
Timepoint [3] 0 0
Weeks 4, 12, 24, 36 and 52
Primary outcome [4] 0 0
Number of Participants With Adverse Events (AEs)
Timepoint [4] 0 0
From the first dose of open-label study drug until 4 weeks after the last dose (up to 56 weeks)
Primary outcome [5] 0 0
Number of Participants With Potentially Clinically Significant Vital Sign Findings
Timepoint [5] 0 0
Weeks 1, 2, 4, 8, 12, 16, 20, 24, 28, 36, 44 and 52
Secondary outcome [1] 0 0
Change From Baseline in Hamilton Depression Scale-24 Item (HAM-D24) Total Score
Timepoint [1] 0 0
Baseline and Weeks 1, 2, 4, 8, 12, 16, 20, 24, 28, 36, 44 and 52.
Secondary outcome [2] 0 0
Change From Baseline in the Montgomery Åsberg Depression Rating Scale (MADRS) Total Score
Timepoint [2] 0 0
Baseline and Weeks 4, 24 and 52
Secondary outcome [3] 0 0
Change From Baseline in the Hamilton Anxiety Scale (HAM-A) Total Score
Timepoint [3] 0 0
Baseline and Weeks 4, 24 and 52
Secondary outcome [4] 0 0
Change From Baseline in the Clinical Global Impression of Severity of Illness Scale
Timepoint [4] 0 0
Baseline and Weeks 4, 24 and 52
Secondary outcome [5] 0 0
Change From Baseline to the Final Visit in 36-item Short-form Health Survey (SF-36)
Timepoint [5] 0 0
Baseline and Week 52
Secondary outcome [6] 0 0
Change From Baseline to the Final Visit in the Sheehan Disability Scale
Timepoint [6] 0 0
Baseline and Week 52
Secondary outcome [7] 0 0
Health Care Resource Utilization Assessed by the Health Economic Assessment Questionnaire
Timepoint [7] 0 0
Baseline and Week 52

Eligibility
Key inclusion criteria
* Has completed the double blind treatment period of either study Lu AA21004_304 (NCT00672620) or LuAA21004_305 (NCT00735709) immediately prior to enrollment in the extension study (ie, the baseline visit is the same visit as the completion visit of the double blind treatment of the preceding protocol).
* Suffers from a major depressive episode as the primary diagnosis according to Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR) criteria (classification code 296.xx) at entry into the prior Lu AA21004_304 or Lu AA21004_305 study.
Minimum age
18 Years
Maximum age
76 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* In addition to meeting the exclusion criteria for studies Lu AA21004_304 or Lu AA21004_305 at the time of enrollment into those studies respectively, with the exception of the criteria prohibiting previous exposure to Lu AA21004 and investigational drugs, and the criteria prohibiting patients with increased intraocular pressure, or risk of acute narrow-angle glaucoma, the following exclusion criteria apply:

* Has Major Depressive Disorder for whom other psychiatric disorders (mania, bipolar disorder, schizophrenia, or any psychotic disorder) have been diagnosed during the prior study.
* The participant, in the investigator's opinion, has a significant risk of suicide and/or a score of =5 points on item 10 (suicidal thoughts) of the Montgomery Åsberg Depression Rating Scale.
* The participant, in the opinion of the investigator, is unlikely to comply with the clinical study protocol or is unsuitable for any reason.
* Has a clinically significant moderate or severe ongoing adverse event related to study medication from the prior study.
* Has used/uses disallowed concomitant medication.

Study design
Purpose of the study
Treatment
Allocation to intervention
Not applicable
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
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
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
1/06/2008
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/08/2010
Sample size
Target
Accrual to date
Final
836
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
- Elizabeth Vale
Recruitment hospital [2] 0 0
- Richmond
Recruitment hospital [3] 0 0
- Southport
Recruitment postcode(s) [1] 0 0
- Elizabeth Vale
Recruitment postcode(s) [2] 0 0
- Richmond
Recruitment postcode(s) [3] 0 0
- Southport
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
California
Country [2] 0 0
United States of America
State/province [2] 0 0
Florida
Country [3] 0 0
United States of America
State/province [3] 0 0
Georgia
Country [4] 0 0
United States of America
State/province [4] 0 0
Illinois
Country [5] 0 0
United States of America
State/province [5] 0 0
Kansas
Country [6] 0 0
United States of America
State/province [6] 0 0
Kentucky
Country [7] 0 0
United States of America
State/province [7] 0 0
Maryland
Country [8] 0 0
United States of America
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Massachusetts
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United States of America
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Mississippi
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United States of America
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New York
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Ohio
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United States of America
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Oklahoma
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United States of America
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Pennsylvania
Country [14] 0 0
United States of America
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Tennessee
Country [15] 0 0
United States of America
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Texas
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United States of America
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Utah
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United States of America
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Washington
Country [18] 0 0
United States of America
State/province [18] 0 0
Wisconsin
Country [19] 0 0
Croatia
State/province [19] 0 0
Osijek
Country [20] 0 0
Croatia
State/province [20] 0 0
Zagreb
Country [21] 0 0
France
State/province [21] 0 0
Bully les Mines
Country [22] 0 0
France
State/province [22] 0 0
Marseille
Country [23] 0 0
France
State/province [23] 0 0
Strasbourg
Country [24] 0 0
Germany
State/province [24] 0 0
Berlin
Country [25] 0 0
Germany
State/province [25] 0 0
Bochum
Country [26] 0 0
Germany
State/province [26] 0 0
Chemnitz
Country [27] 0 0
Germany
State/province [27] 0 0
Huettenberg
Country [28] 0 0
Germany
State/province [28] 0 0
Leipzig
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Germany
State/province [29] 0 0
München
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Germany
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Nuernberg
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Germany
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Wiesbaden
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Korea, Republic of
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Buchon
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Korea, Republic of
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Gyeonggi-do
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Korea, Republic of
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Incheon
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Korea, Republic of
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Seoul
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Latvia
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Liepaja
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Latvia
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Riga
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Latvia
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Sigulda
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Lithuania
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Siauliai
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Lithuania
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Vilnius
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Malaysia
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Kuala Lumpur
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Netherlands
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SchHoogfliet
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Netherlands
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Wildervank
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Netherlands
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Zwijndrecht
Country [45] 0 0
Poland
State/province [45] 0 0
Bialystok
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Poland
State/province [46] 0 0
Leszno
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Poland
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Pruszków
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Poland
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Skórzewo
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Poland
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Torun
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Poland
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Tuszyn
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Russian Federation
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Moscow
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Russian Federation
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Nizhny Novgorod
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Russian Federation
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Novosibirsk
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Russian Federation
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Omsk
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Russian Federation
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St. Petersburg
Country [56] 0 0
Russian Federation
State/province [56] 0 0
Stavropol
Country [57] 0 0
Russian Federation
State/province [57] 0 0
Tomsk
Country [58] 0 0
Serbia
State/province [58] 0 0
Belgrade
Country [59] 0 0
South Africa
State/province [59] 0 0
Bryanston
Country [60] 0 0
South Africa
State/province [60] 0 0
Durban
Country [61] 0 0
South Africa
State/province [61] 0 0
Lyttelton
Country [62] 0 0
South Africa
State/province [62] 0 0
NoordHeuwel
Country [63] 0 0
South Africa
State/province [63] 0 0
Pretoria
Country [64] 0 0
Taiwan
State/province [64] 0 0
Kaohsiung
Country [65] 0 0
Ukraine
State/province [65] 0 0
Dnepropetrovsk
Country [66] 0 0
Ukraine
State/province [66] 0 0
Kiev
Country [67] 0 0
Ukraine
State/province [67] 0 0
Lugansk
Country [68] 0 0
Ukraine
State/province [68] 0 0
Simferopol
Country [69] 0 0
United Kingdom
State/province [69] 0 0
Glasgow

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Takeda
Address
Country
Other collaborator category [1] 0 0
Commercial sector/industry
Name [1] 0 0
H. Lundbeck A/S
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
The purpose of this study is to determine the long-term efficacy and safety of vortioxetine, once daily (QD), in adults with major depressive disorder.
Trial website
https://clinicaltrials.gov/study/NCT00707980
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Medical Director, Clinical Science
Address 0 0
Takeda
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



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/study/NCT00707980