Hetlioz(tasimelteon)
Hetlioz (tasimelteon) is a small molecule pharmaceutical. Tasimelteon was first approved as Hetlioz on 2014-01-31. It is used to treat circadian rhythm sleep disorders in the USA. It has been approved in Europe to treat circadian rhythm sleep disorders. The pharmaceutical is active against melatonin receptor type 1A and melatonin receptor type 1B.
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Commercial
Trade Name
FDA
EMA
Hetlioz (generic drugs available since 2022-12-12)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
hetlioz | New Drug Application | 2020-12-10 |
tasimelteon | ANDA | 2023-01-24 |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
TASIMELTEON, HETLIOZ, VANDA PHARMS INC | |||
2027-12-01 | ODE-330 | ||
2023-12-01 | I-850 | ||
TASIMELTEON, HETLIOZ LQ, VANDA PHARMS INC | |||
2027-12-01 | ODE-329 | ||
2023-12-01 | NP | ||
TASIMELTEON, TASIMELTEON, APOTEX | |||
2023-06-27 | PC |
Patent Expiration
Patent | Expires | Flag | FDA Information |
---|---|---|---|
Tasimelteon, Hetlioz Lq, Vanda Pharms Inc | |||
11202770 | 2040-12-11 | DP | |
Tasimelteon, Hetlioz, Vanda Pharms Inc | |||
10179119 | 2035-08-29 | U-3003 | |
11266622 | 2035-08-29 | U-3003 | |
10376487 | 2035-07-27 | U-2615, U-3007 | |
10071977 | 2035-02-12 | DS, DP | |
10829465 | 2035-02-12 | DS, DP | |
11566011 | 2035-02-12 | DS, DP | |
10610511 | 2034-10-10 | U-2615, U-3007 | |
11141400 | 2034-10-10 | U-2615, U-3007 | |
9730910 | 2034-05-17 | U-2085, U-3005 | |
RE46604 | 2033-01-25 | U-2147 | |
9060995 | 2033-01-25 | U-1710 | |
9539234 | 2033-01-25 | U-1934, U-3004 | |
9549913 | 2033-01-25 | U-1486 | |
9855241 | 2033-01-25 | U-2149 | |
10149829 | 2033-01-25 | U-2477, U-3006 | |
10449176 | 2033-01-25 | U-2149 | |
10610510 | 2033-01-25 | U-2805, U-3009 | |
10945988 | 2033-01-25 | U-2149 | |
10980770 | 2033-01-25 | U-3106, U-3107 | |
11285129 | 2033-01-25 | U-3342, U-3343 | |
11633377 | 2033-01-25 | U-2149, U-3003 |
HCPCS
No data
Clinical
Clinical Trials
23 clinical trials
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Smith-magenis syndrome | D058496 | Orphanet_819 | Q93.88 | 1 | 1 | 1 | — | — | 2 |
Autism spectrum disorder | D000067877 | F84.0 | 1 | — | 1 | — | — | 2 | |
Sleep wake disorders | D012893 | G47 | — | — | 2 | — | — | 2 | |
Sleep initiation and maintenance disorders | D007319 | F51.01 | — | — | 2 | — | — | 2 | |
Major depressive disorder | D003865 | EFO_0003761 | F22 | — | 1 | 1 | — | — | 1 |
Chronobiology disorders | D021081 | — | — | 1 | — | — | 1 | ||
Nervous system diseases | D009422 | G00-G99 | — | — | 1 | — | — | 1 |
Indications Phases 2
No data
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Healthy volunteers/patients | — | 5 | — | — | — | — | 5 | ||
Renal insufficiency | D051437 | HP_0000083 | N19 | 1 | — | — | — | — | 1 |
Hepatic insufficiency | D048550 | 1 | — | — | — | — | 1 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | TASIMELTEON |
INN | tasimelteon |
Description | Tasimelteon is a member of the class of 1-benzofurans that is propionamide in which one of the amide hydrogens is replaced by a [(1R,2R)-2-(2,3-dihydro-1-benzofuran-4-yl)cyclopropyl]methyl group. A melatonin receptor agonist used for the treatment of non-24-hour sleep-wake disorder. It has a role as a melatonin receptor agonist. It is a monocarboxylic acid amide, a member of 1-benzofurans and a member of cyclopropanes. It is functionally related to a propionamide. |
Classification | Small molecule |
Drug class | selective melatonin receptor agonist |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | CCC(=O)NC[C@@H]1C[C@H]1c1cccc2c1CCO2 |
Identifiers
PDB | — |
CAS-ID | 609799-22-6 |
RxCUI | 1490468 |
ChEMBL ID | CHEMBL2103822 |
ChEBI ID | 79042 |
PubChem CID | 10220503 |
DrugBank | DB09071 |
UNII ID | SHS4PU80D9 (ChemIDplus, GSRS) |
Target
Variants
Clinical Variant
No data
Financial
Hetlioz - Vanda Pharmaceuticals
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 258 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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1,988 adverse events reported
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