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 1A, 5-hydroxytryptamine receptor 7, 5-hydroxytryptamine receptor 1B, and sodium-dependent serotonin transporter. In addition, it is known to target 5-hydroxytryptamine receptor 2A, 5-hydroxytryptamine receptor 6, 5-hydroxytryptamine receptor 5A, 5-hydroxytryptamine receptor 2C, 5-hydroxytryptamine receptor 3A, and 5-hydroxytryptamine receptor 1D.
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Commercial
Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
mental disorders | D001523 |
Trade Name
FDA
EMA
Trintellix (generic drugs available since 2021-09-17)
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 |
---|---|---|---|---|
TRINTELLIX | Takeda | N-204447 RX | 2013-09-30 | 3 products, RLD, RS |
Show 1 discontinued
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
trintellix | New Drug Application | 2023-01-05 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
major depressive disorder | EFO_0003761 | D003865 | F22 |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
VORTIOXETINE HYDROBROMIDE, TRINTELLIX, TAKEDA PHARMS USA | |||
2024-01-22 | M-187 | ||
2023-11-13 | M-267 |
Patent Expiration
Patent | Expires | Flag | FDA Information |
---|---|---|---|
Vortioxetine Hydrobromide, Trintellix, Takeda Pharms Usa | |||
9278096 | 2032-03-21 | U-2436 | |
8722684 | 2031-06-30 | DS, DP | |
8969355 | 2027-06-15 | U-1668 | |
9125908 | 2027-06-15 | U-2309 | |
9125909 | 2027-06-15 | U-2309 | |
9125910 | 2027-06-15 | U-2309 | |
9227946 | 2027-06-15 | U-1668 | |
9861630 | 2027-06-15 | U-1668 | |
11458134 | 2027-06-15 | DP | U-3463 |
7144884 | 2026-06-17 | DS, DP | U-1439 |
HCPCS
No data
Clinical
Clinical Trials
100 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 disorder | D003865 | EFO_0003761 | F22 | 4 | 8 | 31 | 13 | 3 | 57 |
Depression | D003863 | F33.9 | 1 | 1 | 2 | 5 | — | 8 | |
Anxiety disorders | D001008 | EFO_0006788 | F41.1 | — | 2 | 6 | 1 | — | 8 |
Healthy volunteers/patients | — | 4 | — | — | 1 | — | 5 | ||
Cognitive dysfunction | D060825 | G31.84 | — | 1 | — | 2 | — | 3 | |
Type 2 diabetes mellitus | D003924 | EFO_0001360 | E11 | — | — | — | 2 | — | 2 |
Depressive disorder | D003866 | EFO_1002014 | F32.A | — | 1 | — | 1 | — | 2 |
Dementia | D003704 | F03 | — | — | — | 1 | — | 1 | |
Post-traumatic stress disorders | D013313 | EFO_0001358 | F43.1 | — | — | — | 1 | — | 1 |
Hot flashes | D019584 | — | — | — | 1 | — | 1 |
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Binge-eating disorder | D056912 | F50.2 | — | 1 | — | — | — | 1 | |
Alcoholism | D000437 | EFO_0003829 | F10.1 | — | 1 | — | — | — | 1 |
Attention deficit disorder with hyperactivity | D001289 | EFO_0003888 | F90 | — | 1 | — | — | — | 1 |
Covid-19 | D000086382 | U07.1 | — | 1 | — | — | — | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | VORTIOXETINE |
INN | vortioxetine |
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 class | antidepressants (fluoxetine type): thioether derivatives |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | Cc1ccc(Sc2ccccc2N2CCNCC2)c(C)c1 |
Identifiers
PDB | — |
CAS-ID | 508233-74-7 |
RxCUI | 1455099 |
ChEMBL ID | CHEMBL2104993 |
ChEBI ID | 76016 |
PubChem CID | 9966051 |
DrugBank | DB09068 |
UNII ID | 3O2K1S3WQV (ChemIDplus, GSRS) |
Target
Agency Approved
HTR1A
HTR1A
HTR7
HTR7
HTR1B
HTR1B
SLC6A4
SLC6A4
Organism
Homo sapiens
Gene name
HTR1A
Gene synonyms
ADRB2RL1, ADRBRL1
NCBI Gene ID
Protein name
5-hydroxytryptamine receptor 1A
Protein synonyms
5-HT1a receptor, 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled, G-21, guanine nucleotide-binding regulatory protein-coupled receptor, Serotonin receptor 1A
Uniprot ID
Mouse ortholog
Htr1a (15550)
5-hydroxytryptamine receptor 1A (Q8BGS4)
Alternate
HTR2A
HTR2A
HTR6
HTR6
HTR5A
HTR5A
HTR2C
HTR2C
HTR3A
HTR3A
HTR1D
HTR1D
Organism
Homo sapiens
Gene name
HTR2A
Gene synonyms
HTR2
NCBI Gene ID
Protein name
5-hydroxytryptamine receptor 2A
Protein synonyms
5-HT2 receptor, 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled, serotonin 5-HT-2A receptor, Serotonin receptor 2A
Uniprot ID
Mouse ortholog
Htr2a (15558)
5-hydroxytryptamine receptor 2A (P35363)
Variants
Clinical Variant
No data
Financial
Trintellix - Takeda
$
€
£
₣
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 1,847 documents
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Safety
Black-box Warning
Black-box warning for: Trintellix
Adverse Events
Top Adverse Reactions
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245 adverse events reported
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