Lumefantrine
Coartem (lumefantrine) is a small molecule pharmaceutical. Lumefantrine was first approved as Coartem on 2009-04-07. It is used to treat falciparum malaria and malaria in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
infections | D007239 |
Trade Name
FDA
EMA
Combinations
Coartem
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Artemether
+
Lumefantrine
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
COARTEM | Novartis | N-022268 RX | 2009-04-07 | 1 products, RLD, RS |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
coartem | New Drug Application | 2020-06-13 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
falciparum malaria | EFO_0007444 | D016778 | B50 |
malaria | EFO_0001068 | D008288 | B54 |
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
HCPCS
No data
Clinical
Clinical Trials
167 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Malaria | D008288 | EFO_0001068 | B54 | 12 | 9 | 24 | 45 | 21 | 106 |
Falciparum malaria | D016778 | EFO_0007444 | B50 | 2 | 10 | 16 | 20 | 6 | 47 |
Vivax malaria | D016780 | EFO_0007445 | B51 | 1 | 1 | 2 | 4 | 1 | 9 |
Hiv infections | D015658 | EFO_0000764 | B20 | 2 | — | 1 | 6 | — | 9 |
Hiv | D006678 | O98.7 | 2 | — | — | 1 | — | 3 | |
Anemia | D000740 | EFO_0004272 | D64.9 | — | — | — | 2 | — | 2 |
Drug interactions | D004347 | — | — | — | 1 | — | 1 | ||
Tuberculosis | D014376 | EFO_0000774 | A15-A19 | — | — | — | 1 | — | 1 |
Schistosomiasis | D012552 | EFO_1001475 | B65 | — | — | — | 1 | — | 1 |
Helminthiasis | D006373 | EFO_1001342 | B65-B83 | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Covid-19 | D000086382 | U07.1 | — | — | 1 | — | — | 1 | |
Fever | D005334 | HP_0001945 | R50.9 | — | — | 1 | — | — | 1 |
Asymptomatic diseases | D058070 | — | 1 | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Healthy volunteers/patients | — | 3 | 1 | — | — | — | 3 | ||
Pharmacokinetics | D010599 | 2 | 1 | — | — | — | 2 | ||
Schistosomiasis haematobia | D012553 | EFO_0007530 | B65.0 | — | 1 | — | — | — | 1 |
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Pneumonia | D011014 | EFO_0003106 | J18 | — | — | — | — | 2 | 2 |
Malnutrition | D044342 | EFO_0008572 | E40-E46 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | LUMEFANTRINE |
INN | lumefantrine |
Description | Lumefantrine is a member of the class of fluorenes that is 9-(p-chlorobenzylidene)-9H-fluorene which is substitutec by chlorine at positions 2 and 7, and by a 2-(dibutylamino)-1-hydroxyethyl group at position 4. An antimalarial drug used in combination with artemether for the treatment of multi-drug resistant strains of falciparum malaria. It has a role as an antimalarial. It is a tertiary amine, a member of monochlorobenzenes, a secondary alcohol and a member of fluorenes. |
Classification | Small molecule |
Drug class | — |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | CCCCN(CCCC)CC(O)c1cc(Cl)cc2c1-c1ccc(Cl)cc1/C2=C/c1ccc(Cl)cc1 |
Identifiers
PDB | — |
CAS-ID | 82186-77-4 |
RxCUI | — |
ChEMBL ID | CHEMBL38827 |
ChEBI ID | 156095 |
PubChem CID | 6437380 |
DrugBank | DB06708 |
UNII ID | F38R0JR742 (ChemIDplus, GSRS) |
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
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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65,198 adverse events reported
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