Neupro(rotigotine)
Neupro (rotigotine) is a small molecule pharmaceutical. Rotigotine was first approved as Neupro on 2006-02-15. It is used to treat parkinson disease and restless legs syndrome in the USA. It has been approved in Europe to treat parkinson disease and restless legs syndrome. The pharmaceutical is active against D(2) dopamine receptor. In addition, it is known to target D(1A) dopamine receptor, D(4) dopamine receptor, D(3) dopamine receptor, and D(1B) dopamine receptor.
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Commercial
Therapeutic Areas
Therapeutic Area | MeSH |
|---|---|
| nervous system diseases | D009422 |
| mental disorders | D001523 |
Trade Name
FDA
EMA
Neupro
Labels
FDA
EMA
Brand Name | Status | Last Update |
|---|---|---|
| neupro | New Drug Application | 2025-06-24 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
|---|---|---|---|
| parkinson disease | EFO_0002508 | D010300 | G20 |
| restless legs syndrome | EFO_0004270 | D012148 | G25.81 |
Agency Specific
FDA
EMA
No data
HCPCS
No data
Clinical
Clinical Trials
110 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Parkinson disease | D010300 | EFO_0002508 | G20 | 4 | 1 | 17 | 7 | 6 | 35 |
| Syndrome | D013577 | — | — | — | 6 | 9 | 2 | 2 | 19 |
| Restless legs syndrome | D012148 | EFO_0004270 | G25.81 | — | 5 | 9 | 2 | 2 | 18 |
| Psychomotor agitation | D011595 | — | — | — | 5 | 9 | 2 | 2 | 18 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Sleep wake disorders | D012893 | — | G47 | — | — | 2 | — | — | 2 |
| Parasomnias | D020447 | — | G47.5 | — | — | 2 | — | — | 2 |
| Chronic kidney failure | D007676 | EFO_0003884 | N18.6 | — | — | 1 | — | — | 1 |
| Kidney diseases | D007674 | EFO_0003086 | N08 | — | — | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Myofascial pain syndromes | D009209 | EFO_1001054 | — | — | 1 | — | — | — | 1 |
| Fibromyalgia | D005356 | EFO_0005687 | M79.1 | — | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Healthy volunteers/patients | — | — | — | 8 | — | — | — | — | 8 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Rotigotine |
| INN | rotigotine |
| Description | 6-{propyl[2-(thiophen-2-yl)ethyl]amino}-5,6,7,8-tetrahydronaphthalen-1-ol is a member of tetralins. |
| Classification | Small molecule |
| Drug class | — |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | CCCN(CCc1cccs1)[C@H]1CCc2c(O)cccc2C1 |
Identifiers
| PDB | — |
| CAS-ID | 99755-59-6 |
| RxCUI | — |
| ChEMBL ID | CHEMBL1303 |
| ChEBI ID | — |
| PubChem CID | 57537 |
| DrugBank | DB05271 |
| UNII ID | 87T4T8BO2E (ChemIDplus, GSRS) |
Target
Variants
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Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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9,963 adverse events reported
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