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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00599911
Registration number
NCT00599911
Ethics application status
Date submitted
28/12/2007
Date registered
24/01/2008
Date last updated
8/11/2016
Titles & IDs
Public title
Dose-finding Study With Lu AA24530 in Major Depressive Disorder
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Scientific title
Randomised, Double-blind, Parallel-group, Placebo-controlled, Active-referenced, Dose-finding Study of Lu AA24530 in Major Depressive Disorder
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Secondary ID [1]
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2007-001071-11
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Secondary ID [2]
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11918A
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Major Depressive Disorder
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Condition category
Condition code
Mental Health
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Depression
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Lu AA24530
Treatment: Drugs - Duloxetine
Treatment: Drugs - Placebo
Experimental: Lu AA24530: 5 mg -
Experimental: Lu AA24530: 10 mg -
Experimental: Lu AA24530: 20 mg -
Active comparator: Duloxetine: 60 mg -
Placebo comparator: Placebo -
Treatment: Drugs: Lu AA24530
per oral, once daily for 6 weeks
Treatment: Drugs: Duloxetine
per oral, once daily for 6 weeks
Treatment: Drugs: Placebo
per oral, once daily for 6 weeks
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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The difference in change from baseline to end of treatment on the Montgomery-Åsberg Depression Rating Scale total score
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Assessment method [1]
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Timepoint [1]
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6 weeks
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Secondary outcome [1]
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Response rate, remission rate, and safety
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Assessment method [1]
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Timepoint [1]
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6 weeks
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Eligibility
Key inclusion criteria
* Major Depressive Episode that has lasted at least 3 months
* Moderate to severe depression
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Minimum age
18
Years
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Maximum age
65
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Any current psychiatric disorder established as the principal diagnosis other than MDD as defined in the DSM-IV-TR and as assessed with the Mini-International Neuropsychiatric Interview (MINI)
* Current or past history of: manic or hypomanic episode, schizophrenia or any other psychotic disorder, including major depression with psychotic features, mental retardation, organic mental disorders, or mental disorders due to a general medical condition as defined in the DSM-IV-TR
* Major Depressive Episode that has been unresponsive to two adequate courses of antidepressant treatment, each of at least 6 weeks duration
* Electroconvulsive therapy within 6 months prior to Baseline
* Ongoing formal cognitive or behavioural therapy, systematic psychotherapy, or plans to initiate such therapy during the study
* Clinically significant unstable illness, for example, hepatic or renal insufficiency, or a cardiovascular, pulmonary, gastrointestinal, endocrine, neurological, infectious, neoplastic, or metabolic disturbance
* The patient is pregnant or breast-feeding
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/10/2007
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/04/2009
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Sample size
Target
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Accrual to date
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Final
652
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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AU002 - Brisbane
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Recruitment hospital [2]
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AU001 - Brisbane
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Recruitment hospital [3]
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AU003 - Dandenc
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Recruitment hospital [4]
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AU004 - Epping
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Recruitment hospital [5]
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AU006 - Malvern
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Recruitment postcode(s) [1]
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4000 - Brisbane
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Recruitment postcode(s) [2]
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4053 - Brisbane
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Recruitment postcode(s) [3]
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3175 - Dandenc
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Recruitment postcode(s) [4]
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3076 - Epping
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Recruitment postcode(s) [5]
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3144 - Malvern
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Recruitment outside Australia
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Austria
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Vienna
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Belgium
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Diest
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Belgium
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Sint-Niklaas
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Mississauga
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Canada
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Oakville
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Canada
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Penticton
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Canada
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Toronto
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Canada
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Vancouver
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Czech Republic
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Brno
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Czech Republic
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Praha 2
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Sternberk
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Finland
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Helsinki
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Finland
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Järvenpää
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Finland
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Tampere
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Rouen
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France
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Savigny sur Orge
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France
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India
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Ahmedabab
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India
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Ahmedabad
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India
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Chennai
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India
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India
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Uppsala
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Dnepropetrovsk
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Kharkov
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Kyiv
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Ukraine
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Lviv
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Ukraine
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Odessa
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
H. Lundbeck A/S
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
The primary purpose of this study is to assess the efficacy in treating patients with Major Depressive Disorder of one or more doses of Lu AA24530 relative to placebo
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Trial website
https://clinicaltrials.gov/study/NCT00599911
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Trial related presentations / publications
Belzeaux R, Gorgievski V, Fiori LM, Lopez JP, Grenier J, Lin R, Nagy C, Ibrahim EC, Gascon E, Courtet P, Richard-Devantoy S, Berlim M, Chachamovich E, Theroux JF, Dumas S, Giros B, Rotzinger S, Soares CN, Foster JA, Mechawar N, Tall GG, Tzavara ET, Kennedy SH, Turecki G. GPR56/ADGRG1 is associated with response to antidepressant treatment. Nat Commun. 2020 Apr 2;11(1):1635. doi: 10.1038/s41467-020-15423-5. Belzeaux R, Fiori LM, Lopez JP, Boucekine M, Boyer L, Blier P, Farzan F, Frey BN, Giacobbe P, Lam RW, Leri F, MacQueen GM, Milev R, Muller DJ, Parikh SV, Rotzinger S, Soares CN, Uher R, Foster JA, Kennedy SH, Turecki G. Predicting Worsening Suicidal Ideation With Clinical Features and Peripheral Expression of Messenger RNA and MicroRNA During Antidepressant Treatment. J Clin Psychiatry. 2019 May 7;80(3):18m12556. doi: 10.4088/JCP.18m12556.
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Public notes
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Contacts
Principal investigator
Name
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Email contact via H. Lundbeck A/S
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Address
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[email protected]
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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/NCT00599911
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