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Life sciences · Phase 3 Trial
ClinicalTrials.gov · September 24, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 3 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT06830044). This is a study registration, not published results. Lead sponsor: Vanda Pharmaceuticals. Recruitment status: RECRUITING. Phase: PHASE3. Study type: INTERVENTIONAL. Enrollment: 500 participants (ESTIMATED). Conditions: Major Depressive Disorder (MDD). Interventions: DRUG: Milsaperidone; DRUG: Placebo. Primary outcome measures: Change from Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) , 6 weeks. Brief summary: The purpose of this study is to determine the efficacy and safety of milsaperidone compared to placebo as adjunctive therapy in patients with Major Depressive Disorder