Evaluation of Efficacy and Safety of Milsaperidone as Adjunctive Therapy in Patients With Major Depressive Disorder

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-65
SponsorVanda Pharmaceuticals

About this trial

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

Eligibility criteria

Qualifiers

Male or female patient 18 to 65 years of age, inclusive;

Meets DSM-5-TR criteria for MDD

Currently having an inadequate response to antidepressant therapy as confirmed by the Investigator using the Antidepressant Treatment Response Questionnaire (ATRQ)

Disqualifiers

Within the patients lifetime, has a confirmed DSM-5-TR psychiatric diagnosis other than MDD

Within 6 months of Screening, has a confirmed DSM-5-TR psychiatric diagnosis other than MDD

Within 12 months of Screening, has had any other psychiatric condition (other than MDD) that has been the main focus of treatment

Trial design

Treatments tested in this trial

  • Milsaperidone
  • Placebo

Treatment groups

500 Participants
are divided into 2 treatment groups

Sponsors and collaborators