A Trial to Measure the Difference in All-cause Hospitalizations for Participants Who Are Using Abilify MyCite Versus Virtual Matched Controls in Adults With Schizophrenia, Bipolar 1 Disorder, and Major Depressive Disorder

Stopped early · Phase 4

Conditions studied: Schizophrenia, Bipolar 1 Disorder, Major Depressive Disorder

In brief

The primary objective of this pragmatic clinical trial (Main Study) was to assess the difference between all-cause hospitalizations in participants using Abilify MyCite versus virtual matched controls. In addition, secondary and exploratory objectives were to assess medication adherence, healthcare utilization and costs, and patient-reported outcomes.

Key facts

Study ID

NCT03643159

Run by

Otsuka Pharmaceutical Development & Commercialization, Inc.

People needed

2

Starts

2018-06-28

Expected to finish

2018-10-17

Last updated by the study team

2019-11-08

Who can join

Age: 18 and older, up to 63. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants are actively enrolled in an Anthem-affiliated commercial, Medicaid, or Medicare health plan with medical and pharmacy benefits.
• Participants must have a smartphone with data plan.
• Participants currently prescribed aripiprazole, or appropriate for aripiprazole treatment.
• Participants must have a current diagnosis of SCH, BP1, or MDD.

You may not qualify if…

• Any participant who participated in another clinical trial within 30 days of enrollment into the current study.
• Females who are breast-feeding and/or who are pregnant at the time of study enrollment, or who plan to become pregnant during the study.
• Participants who are currently being treated with a long-acting injectable antipsychotic.

Where it is running

• Siyan Clinical Research — Santa Rosa, California, United States
• Psychiatric Addiction Curative/PACT Atlanta LLC — Decatur, Georgia, United States
• Georgia Psychiatry and Sleep — Smyrna, Georgia, United States
• Kolade Research Institute — Las Vegas, Nevada, United States
• Signature Research Associates, Inc. — Fairlawn, Ohio, United States

Full record on ClinicalTrials.gov

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