Lumateperone

Clinical data
Pronunciation	/ˌluːməˈtɛpəroʊn/ LOO-mə-TE-pər-ohn
Trade names	Caplyta
Other names	ITI-007; ITI-722
AHFS/Drugs.com	Monograph
MedlinePlus	a620014
License data	US DailyMed: Lumateperone
Routes of administration	By mouth
Drug class	Atypical antipsychotic
ATC code	N05AD10 (WHO)
Legal status
Legal status	US: ℞-only[1]
Pharmacokinetic data
Bioavailability	4.4%[1]
Protein binding	97.4%[1]
Metabolism	MultipleUGTs,CYP450s, andAKR enzymes[1]
Excretion	<1% excreted unchanged in urine[1]
Identifiers
IUPAC name 1-(4-fluorophenyl)-4-((6bR,10aS)-3-methyl-2,3,6b,9,10,10a-hexahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxalin-8(7H)-yl)-1-butanone
CAS Number	313368-91-1 Y
PubChemCID	9821941
DrugBank	DB06077
ChemSpider	7997690
UNII	70BSQ12069
KEGG	D11169
Chemical and physical data
Formula	C24H28FN3O
Molar mass	393.506 g·mol−1
3D model (JSmol)	Interactive image
SMILES CN1CCN2c3c(cccc31)[C@@H]1CN(CCCC(=O)c3ccc(F)cc3)CC[C@@H]12
InChI InChI=1S/C24H28FN3O/c1-26-14-15-28-21-11-13-27(16-20(21)19-4-2-5-22(26)24(19)28)12-3-6-23(29)17-7-9-18(25)10-8-17/h2,4-5,7-10,20-21H,3,6,11-16H2,1H3/t20-,21-/m0/s1 Key:HOIIHACBCFLJET-SFTDATJTSA-N

Lumateperone, sold under the brand nameCaplyta, is anatypical antipsychoticmedication of thepyridopyrroloquinoxaline andbutyrophenone families. It is approved for the treatment ofschizophrenia as well asbipolar depression, as either monotherapy or adjunctive therapy (withlithium orvalproate).^[1] It is developed by Intra-Cellular Therapies, licensed fromBristol-Myers Squibb.^[2] Lumateperone was approved for medical use in the United States in December 2019 with an initial indication for schizophrenia,^[3][4] and became available in February 2020.^[1]

Lumateperone isindicated for the treatment of schizophrenia in adults;^[1] and depressive episodes associated with bipolar I or II disorder (bipolar depression) in adults, as monotherapy and as adjunctive therapy with lithium or valproate.^[1]

In December 2019, the USFood and Drug Administration (FDA) approved lumateperone for the treatment of schizophrenia in adults.^[3][4][5]

In December 2021, the FDA approved lumateperone for the treatment of bipolar depression in adults as monotherapy and as adjunctive therapy withlithium orvalproate.^[1][6]

The most common adverse effects (≥5%) weresomnolence anddry mouth.^[1]

Lumateperone is associated with a low rate of serumaminotransferase elevations during therapy, but has not been linked to instances of clinically apparentacute liver injury.^[7]

Lumateperone acts as anantagonist at5-HT_2A receptors and binds to severaldopamine receptors (D₁,D₂, andD₄) with moderate affinity. It has moderateserotonin transporter reuptake inhibition, which is partly responsible for its antidepressant effect in bipolar disorder and reduction of negative symptoms of schizophrenia.^[1][10] It may also inhibit dopamine transporter reuptake, but more evidence is needed to confirm this.^[8] It has additional off-target antagonism at α1 receptors, without appreciable antimuscarinic or antihistaminergic properties, limiting side effects associated with other atypical antipsychotics, notablymetabolic syndrome andhyperprolactinemia.^[1][8]

Similar toaripiprazole, lumateperone acts as a partial agonist at inhibitory D2autoreceptors and an antagonist at postsynaptic D2 receptors, thereby simultaneously reducing dopamine release and binding to postsynaptic receptors, respectively. However, lumateperone only occupies around 39% of D2 receptors—compared to at least 60-80% D2 occupancy for most antipsychotics to work forpsychosis—and displays regioselectivity for themesolimbic pathway, whose hyperactivity is responsible for the positive symptoms of schizophrenia. This reduces the risk ofextrapyramidal symptoms (EPS) from reduced dopaminergic transmission in thenigrostriatal pathway.^[10][9]

A mechanism that is shared by all other atypical antipsychotics is antagonism of 5HT2A receptors, but, uniquely, lumateperone's affinity for these receptors is 60x higher than its affinity for D2 receptors.^[10] This makes it a highly effective treatment for negative and cognitive symptoms of schizophrenia since 5HT2A antagonism increases dopamine release in themesocortical pathway, which is hypoactive in those with schizophrenia.^[10][8]

Interestingly, lumateperone indirectly augmentsglutamatergic neurotransmission through its activity at D1 receptors, which causesphosphorylation of GluN2B subunits ofNMDA receptors in the mesolimbic pathway. This is significant since NMDA receptor hypofunction, reduced D1 binding, and glutamatergic abnormalities have been implicated in contributing to the cognitive and negative symptoms of schizophrenia.^[10][11]

After taking the medication by mouth, lumateperone reachesmaximum plasma concentrations within 1–2 hours and has a terminal eliminationhalf-life of 18 hours.^[1] Lumateperone is a substrate for numerous metabolic enzymes, including variousglucuronosyltransferase (UGT) isoforms (UGT1A1, 1A4, and 2B15),aldo-keto reductase (AKR) isoforms (AKR1C1,1B10, and1C4), andcytochrome P450 (CYP) enzymes (CYP3A4,2C8, and1A2).^[1]

Lumateperone does not cause appreciable inhibition of any common CYP450 enzymes. It is not a substrate forp-glycoprotein.^[1]

In terms ofchemical structure, lumateperone is apyridopyrroloquinoxaline andbutyrophenone.^[12]

The FDA approved lumateperone in 2019 based on evidence from three clinical trials (Trial 1/NCT01499563, Trial 2/NCT02282761 and Trial 3/NCT02469155) that enrolled 818 adult participants with schizophrenia.^[3] The trials were conducted at 33 sites in the United States.^[3] Trials 1 and 2 provided data on the benefits and side effects of lumateperone, and Trial 3 provided data on side effects only.^[3]

Three trials provided data for the approval of lumateperone.^[3] In each trial, hospitalized participants with schizophrenia were randomly assigned to receive either lumateperone or a comparison treatment (placebo or active comparator) once daily for four weeks (Trials 1 and 2) or six weeks (Trial 3).^[3] Neither the participants nor the health care providers knew which treatment was being given until after the trials were completed.^[3]

Trials 1 and 2 provided data for the assessment of benefits and side effects through four weeks of therapy.^[3] Benefit was assessed by measuring the overall improvement in the symptoms of schizophrenia.^[3] Trial 3 provided data for the assessment of side effects only during six weeks of therapy.^[3]

TwoPhase III lumateperone monotherapy studies were conducted and completed for the treatment of bipolar depression, those being trial Study 401 and Study 404.^[13] A third trial, Study 402, aims to test lumateperone in addition tolithium orvalproate,^[14][15] the data pertaining this trial is due out in 2020.^[16][15]

Study 401 was conducted solely in the United States while Study 404 was a global study and included patients from the US.^[17][18] Of the entire Study 404 population (381 patients), two-thirds were from Russia and Colombia. At the completion of the two monotherapy Phase III trials only Study 404 met its primary endpoint and one of its secondary endpoints.^[19][20] In Study 404, patients received 42 mg lumateperone once daily or placebo for six weeks. Study 404 patients saw an improvement of depressive symptoms compared to placebo as documented by a change inMADRS total score of 4.6.^[21]

• Atypical antipsychotics
• 4-Fluorophenyl compounds
• Ketones
• Pyridopyrroloquinoxalines
• Serotonin-dopamine activity modulators

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