CLINICAL TRIALS PROFILE FOR EDIVOXETINE
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Clinical Trials for Edivoxetine
Trial ID | Title | Status | Sponsor | Phase | Summary |
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NCT00420004 ↗ | A Study for Participants With Major Depression | Completed | Eli Lilly and Company | Phase 2 | This is a study to assess the safety and effectiveness of LY2216684 compared to placebo in treating adults with major depressive disorder. |
NCT00922636 ↗ | A Study of Pediatric Patients With Attention Deficit/Hyperactivity Disorder | Completed | Eli Lilly and Company | Phase 2/Phase 3 | The primary purpose of your child's participation in this study is to determine whether LY2216684 can help pediatric patients with attention-deficit/hyperactivity disorder (ADHD); and assess the safety of LY2216684 and any side effects that might be associated with it. |
NCT00965419 ↗ | A Study of Pediatric Participants With Attention Deficit/Hyperactivity Disorder | Terminated | Eli Lilly and Company | Phase 2/Phase 3 | The primary purpose of the study is to assess long-term safety and tolerability of Edivoxetine in pediatric participants with attention deficit hyperactive disorder (ADHD). |
NCT01155661 ↗ | A Safety Study in Participants With Major Depressive Disorder | Completed | Eli Lilly and Company | Phase 3 | The primary objective of this study is to evaluate the long-term safety and tolerability of LY2216684 administered once daily (QD) in the adjunctive treatment with a selective serotonin reuptake inhibitor (SSRI) for up to approximately 1 year in participants with major depressive disorder (MDD) who are partial responders to their SSRI treatment. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Summary |
Clinical Trial Conditions for Edivoxetine
Condition Name
Clinical Trial Locations for Edivoxetine
Trials by Country
Clinical Trial Progress for Edivoxetine
Clinical Trial Phase
Clinical Trial Sponsors for Edivoxetine
Sponsor Name