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ziprasidone or olanzapine

Medical University of Vienna · FDA-approved active Small molecule

Both ziprasidone and olanzapine are atypical antipsychotics that block dopamine D2 and serotonin 5-HT2A receptors to reduce psychotic symptoms.

Both ziprasidone and olanzapine are atypical antipsychotics that block dopamine D2 and serotonin 5-HT2A receptors to reduce psychotic symptoms. Used for Schizophrenia, Bipolar disorder (acute mania and maintenance), Agitation associated with schizophrenia or bipolar disorder.

At a glance

Generic nameziprasidone or olanzapine
SponsorMedical University of Vienna
Drug classAtypical antipsychotic
TargetDopamine D2 receptor; Serotonin 5-HT2A receptor
ModalitySmall molecule
Therapeutic areaPsychiatry
PhaseFDA-approved

Mechanism of action

Ziprasidone and olanzapine work by antagonizing dopamine D2 receptors in the mesolimbic and mesocortical pathways, which reduces positive symptoms of psychosis, while also blocking serotonin 5-HT2A receptors, which may enhance antipsychotic efficacy and reduce extrapyramidal side effects. Both agents are considered atypical antipsychotics due to their combined dopaminergic and serotonergic activity, distinguishing them from first-generation antipsychotics.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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