Emend, Ivemend(fosaprepitant)
Emend, Ivemend (fosaprepitant) is a small molecule pharmaceutical. Fosaprepitant was first approved as Ivemend on 2008-01-11. It has been approved in Europe to treat neoplasms and vomiting. It is known to target substance-P receptor.
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Commercial
Trade Name
FDA
EMA
Emend (generic drugs available since 2016-06-09)
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 |
---|---|---|
fosaprepitant | New Drug Application | 2022-06-30 |
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
FOSAPREPITANT DIMEGLUMINE, EMEND, MERCK AND CO INC | |||
2025-05-02 | D-186 |
Patent Expiration
No data
ATC Codes
No data
HCPCS
Code | Description |
---|---|
J1453 | Injection, fosaprepitant, 1 mg |
Clinical
Clinical Trials
62 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Vomiting | D014839 | HP_0002013 | R11.1 | 5 | 9 | 11 | 4 | 3 | 31 |
Nausea | D009325 | HP_0002018 | R11.0 | 1 | 3 | 2 | 3 | 2 | 11 |
Postoperative nausea and vomiting | D020250 | EFO_0004888 | 1 | — | 2 | 2 | — | 5 | |
Breast neoplasms | D001943 | EFO_0003869 | C50 | 1 | — | 1 | 1 | — | 3 |
Ovarian neoplasms | D010051 | EFO_0003893 | C56 | — | — | — | 1 | — | 1 |
Uterine neoplasms | D014594 | EFO_0003859 | C55 | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Neoplasms | D009369 | C80 | 1 | 1 | 3 | — | — | 4 | |
Major depressive disorder | D003865 | EFO_0003761 | F22 | — | — | 4 | — | — | 4 |
Nasopharyngeal neoplasms | D009303 | 1 | — | 1 | — | — | 2 | ||
Multiple myeloma | D009101 | C90.0 | 1 | 1 | 1 | — | — | 2 | |
Female genital neoplasms | D005833 | — | — | 1 | — | — | 1 | ||
Digestive system surgical procedures | D013505 | — | — | 1 | — | — | 1 | ||
Uterine cervical neoplasms | D002583 | — | — | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Non-small-cell lung carcinoma | D002289 | — | 1 | — | — | — | 1 | ||
Squamous cell carcinoma of head and neck | D000077195 | — | 1 | — | — | — | 1 | ||
Squamous cell carcinoma | D002294 | — | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Traumatic brain injuries | D000070642 | S06 | 1 | — | — | — | — | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | FOSAPREPITANT |
INN | fosaprepitant |
Description | Fosaprepitant (Emend for Injection (US), Ivemend (EU)) is an antiemetic medication, administered intravenously. It is a prodrug of aprepitant.
|
Classification | Small molecule |
Drug class | phosphoro-derivatives; tachykinin (neurokinin) receptor antagonists: NK1 receptor antagonists |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | C[C@@H](O[C@H]1OCCN(Cc2nn(P(=O)(O)O)c(=O)[nH]2)[C@H]1c1ccc(F)cc1)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 |
Identifiers
PDB | — |
CAS-ID | 172673-20-0 |
RxCUI | 1731071 |
ChEMBL ID | CHEMBL1199324 |
ChEBI ID | 64321 |
PubChem CID | 219090 |
DrugBank | DB06717 |
UNII ID | 6L8OF9XRDC (ChemIDplus, GSRS) |
Target
Agency Approved
No data
Alternate
TACR1
TACR1
Organism
Homo sapiens
Gene name
TACR1
Gene synonyms
NK1R, TAC1R
NCBI Gene ID
Protein name
substance-P receptor
Protein synonyms
neurokinin receptor 1, NK-1 receptor, NK-1R, Tachykinin receptor 1, tachykinin receptor 1 (substance P receptor; neurokinin-1 receptor)
Uniprot ID
Mouse ortholog
Tacr1 (21336)
substance-P receptor (Q8BYR7)
Variants
Clinical Variant
No data
Financial
Emend - Merck Sharp & Dohme
$
€
£
₣
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 520 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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3,594 adverse events reported
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