Enablex, Emselex(darifenacin hydrobromide)
Emselex, Enablex (darifenacin hydrobromide) is a small molecule pharmaceutical. Darifenacin hydrobromide was first approved as Emselex on 2004-10-22. It is used to treat overactive urinary bladder and urge urinary incontinence in the USA. It has been approved in Europe to treat overactive urinary bladder and urge urinary incontinence. It is known to target muscarinic acetylcholine receptor M3 and muscarinic acetylcholine receptor M1.
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Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
urogenital diseases | D000091642 |
signs and symptoms pathological conditions | D013568 |
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Darifenacin hydrobromide
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
ENABLEX | AbbVie | N-021513 DISCN | 2004-12-22 | 2 products, RLD |
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Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
darifenacin | ANDA | 2022-12-01 |
darifenacin | ANDA | 2023-01-25 |
enablex | New Drug Application | 2010-01-01 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
overactive urinary bladder | EFO_1000781 | D053201 | N32.81 |
urge urinary incontinence | EFO_0006865 | D053202 | N39.41 |
Agency Specific
FDA
EMA
No data
Patent Expiration
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HCPCS
No data
Clinical
Clinical Trials
22 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Overactive urinary bladder | D053201 | EFO_1000781 | N32.81 | — | 1 | 3 | 2 | 6 | 12 |
Healthy volunteers/patients | — | 2 | 1 | — | 1 | — | 4 | ||
Nocturia | D053158 | R35.1 | — | — | — | 1 | — | 1 | |
Urinary incontinence | D014549 | HP_0000020 | R32 | — | — | — | 1 | — | 1 |
Spinal cord injuries | D013119 | EFO_1001919 | — | — | — | 1 | — | 1 |
Indications Phases 3
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Multiple sclerosis | D009103 | EFO_0003885 | G35 | — | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Therapeutic equivalency | D013810 | 2 | — | — | — | — | 2 |
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Parkinson disease | D010300 | EFO_0002508 | G20 | — | — | — | — | 1 | 1 |
Renal colic | D056844 | EFO_1001412 | N23 | — | — | — | — | 1 | 1 |
Postoperative pain | D010149 | G89.18 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | DARIFENACIN HYDROBROMIDE |
INN | darifenacin |
Description | Darifenacin is 2-[(3S)-1-Ethylpyrrolidin-3-yl]-2,2-diphenylacetamide in which one of the hydrogens at the 2-position of the ethyl group is substituted by a 2,3-dihydro-1-benzofuran-5-yl group. It is a selective antagonist for the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions, and is used as the hydrobromide salt in the management of urinary incontinence. It has a role as a muscarinic antagonist and an antispasmodic drug. It is a member of 1-benzofurans, a member of pyrrolidines and a monocarboxylic acid amide. |
Classification | Small molecule |
Drug class | muscarinic receptor antagonists |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | Br.NC(=O)C(c1ccccc1)(c1ccccc1)[C@@H]1CCN(CCc2ccc3c(c2)CCO3)C1 |
Identifiers
PDB | — |
CAS-ID | 133099-04-4 |
RxCUI | 136198 |
ChEMBL ID | CHEMBL1200935 |
ChEBI ID | 31455 |
PubChem CID | 444031 |
DrugBank | DB00496 |
UNII ID | APG9819VLM (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
Variants
Clinical Variant
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Financial
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Trends
PubMed Central
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Safety
Black-box Warning
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Adverse Events
Top Adverse Reactions
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535 adverse events reported
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