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Drug ReportsVortioxetine
Trintellix, Brintellix(vortioxetine)
Brintellix, Trintellix (vortioxetine) is a small molecule pharmaceutical. Vortioxetine was first approved as Trintellix on 2013-09-30. It is used to treat major depressive disorder in the USA. It has been approved in Europe to treat major depressive disorder. The pharmaceutical is active against 5-hydroxytryptamine receptor 1B, sodium-dependent serotonin transporter, 5-hydroxytryptamine receptor 7, and 5-hydroxytryptamine receptor 1A. In addition, it is known to target 5-hydroxytryptamine receptor 5A, 5-hydroxytryptamine receptor 6, 5-hydroxytryptamine receptor 2A, and 5-hydroxytryptamine receptor 1D.
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Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
mental disordersD001523
Trade Name
FDA
EMA
Trintellix
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Vortioxetine hydrobromide
Tradename
Company
Number
Date
Products
TRINTELLIXTakedaN-204447 RX2013-09-30
3 products, RLD, RS
Show 1 discontinued
Labels
FDA
EMA
No data
Indications
FDA
EMA
Agency Specific
FDA
EMA
Expiration
Code
VORTIOXETINE HYDROBROMIDE, TRINTELLIX, TAKEDA PHARMS USA
2024-01-22M-187
2023-11-13M-267
Patent Expiration
Patent
Expires
Flag
FDA Information
Vortioxetine Hydrobromide, Trintellix, Takeda Pharms Usa
92780962032-03-21U-2436
87226842031-06-30DS, DP
89693552027-06-15U-1668
91259082027-06-15U-2309
91259092027-06-15U-2309
91259102027-06-15U-2309
92279462027-06-15U-1668
98616302027-06-15U-1668
114581342027-06-15DPU-3463
71448842026-06-17DS, DPU-1439
ATC Codes
N: Nervous system drugs
N06: Psychoanaleptics
N06A: Antidepressants
N06AX: Other antidepressants in atc
N06AX26: Vortioxetine
HCPCS
No data
Clinical
Clinical Trials
106 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Major depressive disorderD003865EFO_0003761F22493113863
DepressionD003863F33.922259
Anxiety disordersD001008EFO_0006788F41.12618
Healthy volunteers/patients415
Cognitive dysfunctionD060825HP_0001268G31.84123
Type 2 diabetes mellitusD003924EFO_0001360E1122
Depressive disorderD003866EFO_1002014F32.A112
Bipolar disorderD001714EFO_0000289F30.9112
DementiaD003704EFO_0003862F0311
Post-traumatic stress disordersD013313EFO_0001358F43.111
Show 8 more
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Treatment outcomeD01689611
Radiation injuriesD011832T6611
Hoarding disorderD000067836F42.311
Drug therapyD004358111
Burning mouth syndromeD002054EFO_100085011
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Binge-eating disorderD056912F50.211
AlcoholismD000437EFO_0003829F10.111
Attention deficit disorder with hyperactivityD001289EFO_0003888F9011
Covid-19D000086382U07.111
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Coronary artery diseaseD003324I25.111
PharmacokineticsD01059911
Hepatic insufficiencyD04855011
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Drug-related side effects and adverse reactionsD064420T88.711
Drug interactionsD00434711
NeoplasmsD009369C8011
Magnetic resonance imagingD00827911
Electroconvulsive therapyD00456511
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameVortioxetine
INNvortioxetine
Description
Vortioxetine is an N-arylpiperazine in which the aryl group is specified as 2-[(2,4-dimethylphenyl)sulfanyl]phenyl. Used (as its hydrobromide salt) for treatment of major depressive disorder. It has a role as an antidepressant, an anxiolytic drug, a serotonergic agonist and a serotonergic antagonist. It is a N-arylpiperazine and an aryl sulfide. It is a conjugate base of a vortioxetine(1+).
Classification
Small molecule
Drug classantidepressants (fluoxetine type): thioether derivatives
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Cc1ccc(Sc2ccccc2N2CCNCC2)c(C)c1
Identifiers
PDB
CAS-ID508233-74-7
RxCUI
ChEMBL IDCHEMBL2104993
ChEBI ID76016
PubChem CID9966051
DrugBankDB09068
UNII ID3O2K1S3WQV (ChemIDplus, GSRS)
Target
Agency Approved
HTR1B
HTR1B
SLC6A4
SLC6A4
HTR7
HTR7
HTR1A
HTR1A
Organism
Homo sapiens
Gene name
HTR1B
Gene synonyms
HTR1DB
NCBI Gene ID
Protein name
5-hydroxytryptamine receptor 1B
Protein synonyms
5-HT-1D-beta, 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled, S12, Serotonin 1D beta receptor, Serotonin receptor 1B
Uniprot ID
Mouse ortholog
Htr1b (15551)
5-hydroxytryptamine receptor 1B (P28334)
Alternate
HTR5A
HTR5A
HTR6
HTR6
HTR2A
HTR2A
HTR1D
HTR1D
Organism
Homo sapiens
Gene name
HTR5A
Gene synonyms
NCBI Gene ID
Protein name
5-hydroxytryptamine receptor 5A
Protein synonyms
5-HT-5, 5-HT-5A, 5-hydroxytryptamine (serotonin) receptor 5A, G protein-coupled, Serotonin receptor 5A
Uniprot ID
Mouse ortholog
Htr5a (15563)
5-hydroxytryptamine receptor 5A (Q3URB0)
Variants
No data
Financial
Revenue by drug
$
£
Trintellix Takeda
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Estimated US medical usage
Vortioxetine
Total medical expenditures per year (USD, in millions)
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Number of persons purchased
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Number of purchases
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Refill frequency
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Price per prescription (USD)
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 2,341 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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12,183 adverse events reported
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