Aripiprazole (Abilify, Abilify Discmelt)
is an
atypical antipsychotic and
antidepressant used in the treatment of
schizophrenia,
bipolar disorder, and
clinical depression. It was approved by the
Food and Drug Administration (FDA) for schizophrenia on
November 15, 2002, for acute
manic
and
mixed episodes associated with bipolar disorder on October
1, 2004, and as an adjunct for
major depressive disorder on November 20, 2007.[1]
Aripiprazole was developed by
Otsuka in
Japan,
and in the
United States,
Otsuka America markets it jointly with
Bristol-Myers Squibb.
Indications
and Usage
Schizophrenia
Aripiprazole has been approved by the FDA for the treatment
of schizophrenia.[2]
Bipolar disorder
Aripiprazole has been approved by the FDA for the treatment
of acute manic and mixed episodes, in both pediatric patients
aged 10–17 and in adults.[3]
Several double-blind, placebo-controlled trials support this
use.[4][5][6][7]
In addition, it is often used as maintenance therapy, either on
its own or in conjunction with a
mood stabilizer such as
lithium or
valproate. This use is also supported by a handful of
studies.[8][9]
Aripiprazole is at least as effective as
haloperidol at reducing manic symptoms,[10][unreliable
source?] and is much better tolerated by patients.[11]
Aripiprazole's use as a monotherapy in bipolar depression is
more controversial. While a few pilot studies have found some
effectiveness[12][13]
(with one finding a reduction in
anhedonia symptoms[14]),
two large, double-blind, placebo-controlled studies found no
difference between aripiprazole and placebo.[15]
One study reported depression as a side effect of the drug.[16]
Major Depression (Unipolar Depression)
In 2007, aripiprazole was approved by the FDA for the
treatment of unipolar depression when used adjunctively with an
antidepressant medication.
[17] It has not been
FDA-approved for use as monotherapy in unipolar depression.
Autism
In 2009, the United States FDA approved Abilify to treat
autism.[18]
It was approved on the basis of two studies that showed it
reduced aggression towards others, self-injury, quickly changing
moods, irritability, and temper tantrums in autistic men and
women 6–17 years of age.
Pharmacology
Aripiprazole's
mechanism of action is different from those of the other
FDA-approved
atypical antipsychotics (e.g.,
clozapine,
olanzapine,
quetiapine,
ziprasidone, and
risperidone). Rather than
antagonizing the
D2 receptor, aripiprazole acts as a D2
partial agonist.[19][20]
Aripiprazole is also a partial agonist at the
5-HT1A receptor, and like the other atypical
antipsychotics displays an antagonist profile at the
5-HT2A receptor.[21][22]
It also antagonizes the
5-HT77 receptor and acts as a partial agonist at
the
5-HT2C receptor, both with high affinity. The
latter action may underly the minimal weight gain seen in the
course of therapy.[23]
Aripiprazole has moderate affinity for histamine and
α-adrenergic receptors and for the
serotonin transporter, and no appreciable affinity for
cholinergic muscarinic receptors.[24]
D2 and
D3 receptor occupancy levels are high, with
average levels ranging between ~71% at 2 mg/day to ~96% at
40 mg/day.[25][26]
Most atypical antipsychotics bind preferentially to
extrastriatal receptors, but aripiprazole appears to be less
preferential in this regard, as binding rates are high
throughout the brain.[27]
Recently, it has been demonstrated that in 5-HT7
receptor
knockout mice, aripiprazole does not reduce immobility time
in the
forced swim test (FST), and actually increases it.[28][29]
This implicates 5-HT7 antagonism as playing a major
role in aripiprazole's antidepressant effects, similarly to
amisulpride.[28][29][30]
Pharmacokinetics
Aripiprazole displays linear kinetics and has an elimination
half-life of approximately 75 hours. Steady-state plasma
concentrations are achieved in about 14 days. Cmax (maximum
plasma concentration) is achieved 3–5 hours after oral dosing.
Bioavailability of the oral tablets is about 90% and the
drug undergoes extensive hepatic metabolization
(dehydrogenation, hydroxylation, and N-dealkylation),
principally by the enzymes
CYP2D6 and
CYP3A4. Its only known active metabolite is
dehydro-aripiprazole, which typically accumulates to
approximately 40% of the aripiprazole concentration. The
parenteral drug is excreted only in traces, and its metabolites,
active or not, are excreted via feces and urine.[24]
Patent status
Otsuka's US patent on aripiprazole expires on October 20,
2014;[31]
however, due to a pediatric extension, a generic will not become
available until at least April 20, 2015.[3]
Barr Laboratories (now
Teva Pharmaceuticals) initiated a patent challenge under the
Hatch-Waxman Act in March 2007.[32]
This challenge is still in court as of 14 August 2009.
Side effects
Akathisia, headache, unusual tiredness or weakness, nausea,
vomiting, an uncomfortable feeling in the stomach, constipation,
light-headedness,
insomnia, sleepiness, shaking, and blurred vision.
Uncontrollable twitching or jerking movements, tremors,
seizure, and weight gain. Some people may feel dizzy, especially
when getting up from a lying or sitting position, or may
experience a fast heart rate.
Neuroleptic malignant syndrome (Combination of
fever,
muscle stiffness,
faster breathing,
sweating, reduced consciousness, and sudden change in
blood pressure and
heart rate.)
Tardive dyskinesia (As with all antipsychotic medication,
patients using aripiprazole may develop the permanent
neurological disorder tardive dyskinesia.[33][34][35])
Stroke (While taking aripiprazole some elderly patients with
dementia have suffered from
stroke or
'mini' stroke.)
Other elderly patients may experience high
blood sugar or the onset or worsening of
diabetes.
Allergic reaction (such as swelling in the
mouth
or
throat,
itching,
rash),
increased production of
saliva,
speech disorder,
nervousness,
agitation,
fainting, reports of abnormal
liver test values,
inflammation of the pancreas,
muscle pain, weakness, stiffness, or cramps.
Overdosage
Children or adults who ingested acute overdoses have usually
manifested central nervous system depression ranging from mild
sedation to coma; serum concentrations of aripiprazole and
dehydroaripiprazole in these patients were elevated by up to 3-4
fold over normal therapeutic levels, yet no deaths have yet been
recorded.[36]
Drug
interactions
Aripiprazole is a substrate of
CYP2D6 and
CYP3A4. Coadministration with medications that inhibit (e.g.
paroxetine,
fluoxetine) or induce (e.g.
carbamazepine) these metabolic enzymes are known to increase
and decrease, respectively, plasma levels of aripiprazole.[37]
As such, anyone taking Abilify should be aware that their dosage
of Abilify may need to be decreased.
Aripiprazole may change the subjective effects of alcohol.
One study[38]
found that aripiprazole increased the sedative effect and
reduced the sense of euphoria normally associated with alcohol
consumption. However, another alcohol study[39]
found that there was no difference in subjective effect between
a placebo group and a group taking aripiprazole.
Dosage forms
- Intramuscular injection, solution: 7.5 mg/mL (1.3 mL)
- Solution, oral: 1 mg/mL (150 mL) [contains
propylene glycol,
sucrose 400 mg/mL, and
fructose 200 mg/mL; orange cream flavor]
- Tablet: 2 mg, 5 mg, 10 mg, 15 mg, 20 mg, 30 mg
- Tablet, orally disintegrating: 10 mg [contains
phenylalanine 1.12 mg; creme de vanilla flavor]; 15 mg
[contains phenylalanine 1.68 mg; creme de vanilla flavor]
Chemistry

U.S. Patent 5,006,528
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Ethylone •
Fenethylline •
Fenproporex •
Flephedrone •
Fludorex •
Furfenorex •
Hordenine •
Lophophine (Homomyristicylamine) •
Mefenorex •
Mephedrone •
Methamphetamine (Desoxyephedrine,
Methedrine;
Dextromethamphetamine,
Levomethamphetamine) •
Methcathinone (Methylpropion) •
Methedrone •
Methoxymethylenedioxyamphetamine (MMDA)
•
Methoxymethylenedioxymethamphetamine
(MMDMA) •
Methylbenzodioxolylbutanamine (MBDB) •
Methylenedioxyamphetamine (MDA;
Tenamfetamine) •
Methylenedioxyethylamphetamine (MDEA) •
Methylenedioxyhydroxyamphetamine (MDOH)
•
Methylenedioxymethamphetamine (MDMA) •
Methylenedioxymethylphenethylamine
(MDMPEA; Homarylamine) •
Methylenedioxyphenethylamine (MDPEA;
Homopiperonylamine) •
Methylone •
Ortetamine •
Parabromoamphetamine (PBA) •
Parachloroamphetamine (PCA) •
Parafluoroamphetamine (PFA) •
Parafluoromethamphetamine (PFMA) •
Parahydroxyamphetamine (PHA) •
Paraiodoamphetamine (PIA) •
Paramethoxyamphetamine (PMA) •
Paramethoxyethylamphetamine (PMEA) •
Paramethoxymethamphetamine (PMMA) •
Paredrine (Norpholedrine, Oxamphetamine)
•
Phenethylamine (PEA) •
Pholedrine •
Phenpromethamine •
Prenylamine •
Propylamphetamine •
Tiflorex (Flutiorex) •
Tyramine (TRA) •
Xylopropamine •
Zylofuramine; Piperazines:
2,5-Dimethoxy-4-bromobenzylpiperazine
(2C-B-BZP) •
Benzylpiperazine (BZP) •
Methoxyphenylpiperazine (MeOPP;
Paraperazine) •
Methylbenzylpiperazine (MBZP) •
Methylenedioxybenzylpiperazine (MDBZP;
Piperonylpiperazine); Others:
2-Amino-1,2-dihydronaphthalene (2-ADN) •
2-Aminoindane (2-AI) •
2-Aminotetralin (2-AT) •
4-Benzylpiperidine (4-BP) •
Clofenciclan •
Cyclopentamine •
Cypenamine •
Cyprodenate •
Feprosidnine •
Gilutensin •
Heptaminol •
Hexacyclonate •
Indanylaminopropane (IAP) •
Indanorex •
Isometheptene •
Methylhexanamine •
Naphthylaminopropane (NAP) •
Octodrine •
Phthalimidopropiophenone •
Propylhexedrine ( Levopropylhexedrine)
•
Tuaminoheptane (Tuamine)
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Enzyme
Inhibitors |
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Others |
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Histaminergics |
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Receptor
Ligands |
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Agonists:
2-Pyridylethylamine •
Betahistine •
Histamine •
HTMT ���
UR-AK49
Antagonists: 1st
Generation:
4-Methyldiphenhydramine •
Alimemazine •
Antazoline •
Azatadine •
Bamipine •
Benzatropine (Benztropine) •
Bepotastine •
Bromazine •
Brompheniramine •
Buclizine •
Captodiame •
Carbinoxamine •
Chlorcyclizine •
Chloropyramine •
Chlorothen •
Chlorpheniramine •
Chlorphenoxamine •
Cinnarizine •
Clemastine •
Clobenzepam •
Clocinizine •
Cyclizine •
Cyproheptadine •
Dacemazine •
Deptropine •
Dexbrompheniramine •
Dexchlorpheniramine •
Dimenhydrinate •
Dimetindene •
Diphenhydramine •
Diphenylpyraline •
Doxylamine •
Embramine •
Etybenzatropine
(Ethylbenztropine) •
Etymemazine •
Histapyrrodine •
Hydroxyethylpromethazine •
Hydroxyzine •
Isopromethazine •
Isothipendyl •
Meclizine •
Mepyramine (Pyrilamine) •
Mequitazine •
Methafurylene •
Methapyrilene •
Methdilazine •
Moxastine •
Niaprazine •
Orphenadrine •
Oxatomide •
Oxomemazine •
Phenindamine •
Pheniramine •
Phenyltoloxamine •
Pimethixene •
Promethazine •
Propiomazine •
Pyrrobutamine •
Talastine •
Thenalidine ���
Thenyldiamine •
Thiazinamium •
Thonzylamine •
Tolpropamine •
Tripelennamine •
Triprolidine; 2nd Generation:
Acrivastine •
Astemizole •
Azelastine •
Cetirizine •
Clemizole •
Clobenztropine •
Ebastine •
Emedastine •
Epinastine •
Ketotifen •
Latrepirdine •
Levocabastine •
Loratadine •
Mebhydrolin •
Mizolastine •
Olopatadine •
Rupatadine •
Setastine •
Terfenadine; 3rd Generation:
Desloratadine •
Fexofenadine •
Levocetirizine; Miscellaneous:
Tricyclic Antidepressants ( Amitriptyline,
Doxepin,
Trimipramine, etc) •
Tetracyclic Antidepressants ( Mianserin,
Mirtazapine, etc) •
Serotonin Antagonists and Reuptake
Inhibitors ( Trazodone,
Nefazodone) •
Typical Antipsychotics ( Chlorpromazine,
Thioridazine, etc) •
Atypical Antipsychotics ( Clozapine,
Olanzapine,
Quetiapine, etc)
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Reuptake
Inhibitors |
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Enzyme
Inhibitors |
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Others |
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[hide]
Serotonergics |
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Receptor
ligands |
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Agonists: Azapirones:
Alnespirone •
Binospirone •
Buspirone •
Enilospirone •
Eptapirone •
Gepirone •
Ipsapirone •
Perospirone ��
Revospirone •
Tandospirone •
Tiospirone •
Umespirone •
Zalospirone; Antidepressants:
Etoperidone •
Nefazodone •
Trazodone; Antipsychotics:
Aripiprazole •
Asenapine •
Clozapine •
Quetiapine •
Ziprasidone; Ergolines:
Dihydroergotamine •
Ergotamine •
Lisuride •
Methysergide •
LSD; Tryptamines:
5-CT •
5-MeO-DMT •
5-MT •
Bufotenin •
DMT •
Psilocin •
Psilocybin; Others:
8-OH-DPAT •
Adatanserin •
Befiradol •
Dimemebfe •
Ebalzotan •
Eltoprazine •
F-11,461 •
F-12,826 •
F-13,714 •
F-14,679 •
F-15,599 •
Flesinoxan •
Flibanserin •
Lesopitron •
Lu AA21004 •
LY-293,284 •
LY-301,317 •
MKC-242 •
NBUMP •
Osemozotan •
Oxaflozane •
Pardoprunox •
Piclozotan •
Rauwolscine •
Repinotan ��
Roxindole •
RU-24969 •
S-15535 •
Sarizotan •
SSR-181,507 •
Sunepitron •
U-92016A •
Urapidil •
Vilazodone •
Xaliproden •
Yohimbine
Antagonists:
Antipsychotics:
Iloperidone •
Risperidone •
Sertindole; Beta Blockers:
Alprenolol •
Cyanopindolol •
Iodocyanopindolol •
Oxprenolol •
Pindobind •
Pindolol •
Propranolol •
Tertatolol; Others:
AV965 •
BMY-7378 •
Dotarizine •
Flopropione •
GR-46611 •
Isamoltane •
Lecozotan •
Metitepine/Methiothepin •
MPPF •
NAN-190 •
PRX-00023 •
Robalzotan •
S-15535 •
SB-649915 •
SDZ 216-525 •
Spiperone •
Spiramide •
Spiroxatrine •
UH-301 •
WAY-100,135 •
WAY-100,635 •
Xylamidine
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Agonists: Lysergamides:
Dihydroergotamine •
Methysergide; Triptans:
Almotriptan •
Avitriptan •
Eletriptan •
Frovatriptan •
Naratriptan •
Rizatriptan •
Sumatriptan •
Zolmitriptan; Tryptamines:
5-CT •
5-MT; Others:
CP-135,807 •
CP-286,601 •
GR-46611 •
L-694,247 •
L-772,405 •
PNU-109,291 •
PNU-142,633
Antagonists: Lysergamides:
Metergoline; Others:
Alniditan
BRL-15572 •
GR-127,935 •
Ketanserin •
LY-310,762 •
LY-367,642 •
LY-456,219 •
LY-456,220 •
Metitepine/Methiothepin •
Ritanserin •
Yohimbine •
Ziprasidone
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Agonists: Phenethylamines:
2C-B •
2C-E •
2C-I •
2C-T-2 •
2C-T-7 •
2C-T-21 •
DOB •
DOC •
DOI •
DOM •
MDA •
MDMA •
Mescaline; Piperazines:
Aripiprazole •
mCPP •
TFMPP; Tryptamines:
5-CT •
5-MeO-α-ET •
5-MeO-α-MT •
5-MeO-DET •
5-MeO-DiPT •
5-MeO-DMT ���
5-MeO-DPT •
5-MT •
α-ET •
α-Methyl-5-HT •
α-MT •
Bufotenin •
DET •
DiPT •
DMT •
DPT ��
Psilocin •
Psilocybin; Others:
A-372,159 •
AL-38022A •
CP-809,101 •
Dimemebfe •
Lorcaserin•
Medifoxamine •
MK-212 •
ORG-37,684 •
Oxaflozane •
PNU-22394 •
Ro60-0175 •
Vabicaserin •
WAY-629 •
WAY-161,503 •
YM-348
Antagonists: Atypical
Antipsychotics:
Clozapine •
Iloperidone •
Melperone •
Olanzapine •
Paliperidone •
Pimozide •
Quetiapine •
Risperidone •
Sertindole •
Ziprasidone •
Zotepine; Typical
Antipsychotics:
Chlorpromazine •
Loxapine •
Pipamperone; Antidepressants:
Agomelatine •
Amitriptyline •
Amoxapine •
Etoperidone •
Fluoxetine •
Mianserin •
Mirtazapine •
Nefazodone •
Nortriptyline •
Trazodone; Others:
Adatanserin •
Cinanserin •
Cyproheptadine •
Deramciclane •
Dotarizine •
Eltoprazine •
Esmirtazapine •
FR-260,010 •
Ketanserin •
Ketotifen •
Latrepirdine •
Lu AA24530 •
Metitepine/Methiothepin •
Methysergide •
Pizotifen •
Ritanserin •
RS-102,221 •
SB-200,646 •
SB-206,553 •
SB-221,284 •
SB-228,357 •
SB-242,084 •
SB-243,213 •
SDZ SER-082 •
Xylamidine
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Agonists: Lysergamides:
Dihydroergotamine •
Ergotamine •
Lisuride •
LSD •
Mesulergine •
Metergoline •
Methysergide; Tryptamines:
2-Methyl-5-HT •
5-BT •
5-CT •
5-MT •
Bufotenin •
E-6801 •
E-6837 •
EMD-386,088 •
EMDT •
LY-586,713 •
N-Methyl-5-HT •
Tryptamine •
WAY-181,187 •
WAY-208,466
Antagonists:
Antidepressants:
Amitriptyline •
Amoxapine •
Clomipramine •
Doxepin •
Mianserin •
Nortriptyline; Atypical
Antipsychotics:
Aripiprazole •
Asenapine •
Clozapine •
Fluperlapine •
Iloperidone •
Olanzapine •
Tiospirone; Typical
Antipsychotics:
Chlorpromazine •
Loxapine; Others:
BGC20-760 •
BVT-5182 •
BVT-74316 •
EGIS-12233 •
GW-742,457 •
Ketanserin •
Latrepirdine •
Lu AE58054 •
Metitepine/Methiothepin •
MS-245 •
PRX-07034 •
Ritanserin •
Ro 04-6790 •
Ro 63-0563 •
SB-258,585 •
SB-271,046 •
SB-357,134 •
SB-399,885 •
SB-742,457
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Reuptake
Inhibitors |
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Releasing
Agents |
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