EMICERFONT
Emicerfont is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Events Timeline
5D
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3M
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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
No data
Clinical
Clinical Trials
10 clinical trials
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Indications Phases 4
No data
Indications Phases 3
No data
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Irritable bowel syndrome | D043183 | EFO_0000555 | K58 | 1 | 3 | — | — | — | 4 |
| Social phobia | D000072861 | EFO_1001917 | F40.1 | 2 | 1 | — | — | — | 3 |
| Syndrome | D013577 | — | — | 1 | 2 | — | — | — | 3 |
| Anxiety disorders | D001008 | EFO_0006788 | F41.1 | 1 | 1 | — | — | — | 2 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Healthy volunteers/patients | — | — | — | 3 | — | — | — | — | 3 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | EMICERFONT |
| INN | emicerfont |
| Description | Emicerfont is an aromatic amine and a tertiary amino compound. |
| Classification | Small molecule |
| Drug class | CRF-1 (corticotropin releasing factor) receptor antagonists |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | COc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C)c1 |
Identifiers
| PDB | — |
| CAS-ID | 786701-13-1 |
| RxCUI | — |
| ChEMBL ID | CHEMBL514270 |
| ChEBI ID | — |
| PubChem CID | 11223423 |
| DrugBank | DB12910 |
| UNII ID | OJ8EG4264P (ChemIDplus, GSRS) |
Target
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Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 51 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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