Clinical trial
An 8 Week Double Blind, Placebo-Controlled, Parallel Group, Fixed Dosage Study to Evaluate the Efficacy and Safety of Armodafinil Treatment (150mg/Day) as Adjunctive Therapy in Adults With Major Depression Associated With Bipolar I Disorder
NCT00481195 is registered in ClinicalTrials.gov with Cephalon as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- An 8 Week Double Blind, Placebo-Controlled, Parallel Group, Fixed Dosage Study to Evaluate the Efficacy and Safety of Armodafinil Treatment (150mg/Day) as Adjunctive Therapy in Adults With Major Depression Associated With Bipolar I Disorder
- Lead sponsor
- Cephalon
- Phase
- Phase 2
- Overall status
- Completed
- Start date
- June 30, 2007
- Completion date
- December 31, 2008
- Enrollment
- 257 (actual)
- Sites
- 55
Conditions
As the registry lists them; a condition with its own page is linked.
bipolar i depression