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Abilify MyCite®

Otsuka Pharmaceutical Development & Commercialization, Inc. · FDA-approved active Small molecule

Abilify MyCite is an ingestible tablet formulation of aripiprazole, a dopamine D2 and serotonin 5-HT1A receptor partial agonist, equipped with an ingestible sensor that tracks medication adherence.

Abilify MyCite is an ingestible tablet formulation of aripiprazole, a dopamine D2 and serotonin 5-HT1A receptor partial agonist, equipped with an ingestible sensor that tracks medication adherence. Used for Schizophrenia, Bipolar I disorder (acute manic or mixed episodes), Major depressive disorder (adjunctive treatment).

At a glance

Generic nameAbilify MyCite®
Also known asOPC-14597 Digital
SponsorOtsuka Pharmaceutical Development & Commercialization, Inc.
Drug classAtypical antipsychotic with digital adherence monitoring
TargetDopamine D2 receptor, serotonin 5-HT1A receptor
ModalitySmall molecule
Therapeutic areaPsychiatry
PhaseFDA-approved

Mechanism of action

Aripiprazole works by acting as a partial agonist at dopamine D2 receptors and serotonin 5-HT1A receptors, helping to restore balance in neurotransmitter activity in the brain. The MyCite formulation includes an ingestible sensor that detects when the medication is ingested and transmits this information to a wearable patch and mobile app, enabling real-time monitoring of medication adherence. This digital health component is designed to improve treatment outcomes by providing patients, caregivers, and healthcare providers with objective adherence data.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results