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NCT00545142: SMART-A

Multi-center, Single Arm, Open Phase IV Clinical Trial to Evaluate the Efficacy and Safety of Co-administration of Abilify With Depakote in the 6-week Treatment of Acute Mania in Patients With Bipolar Disorder

Completed Phase 4 Last updated 24 June 2010
What this trial tests

Phase 4 trial testing Abilify(Aripiprazole) in Bipolar Disorder in 280 participants. Completed in 1 June 2010.

Timeline
1 October 2007
Primary endpoint
1 June 2010
1 June 2010

Quick facts

Lead sponsorKorea Otsuka Pharmaceutical Co., Ltd.
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment280
Start date1 October 2007
Primary completion1 June 2010
Estimated completion1 June 2010
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Korea Otsuka Pharmaceutical Co., Ltd. — full company profile →

Who can join

Adults 18 to 65, any sex, with Bipolar Disorder. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

To demonstrate the efficacy and safety of co-administration of Abilify(aripiprazole) with Depakote(divalproate) in the acute phase of 6-week treatment of acute mania in patients with bipolar disorder.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Bipolar Disorder

Currently open trials in the same condition.

Other Korea Otsuka Pharmaceutical Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00545142.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing