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Drug ReportsVinflunine
Vinflunine
Javlor (vinflunine) is a small molecule pharmaceutical. Vinflunine was first approved as Javlor on 2009-09-21. It has been approved in Europe to treat transitional cell carcinoma and urologic neoplasms.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
neoplasmsD009369
urogenital diseasesD000091642
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)
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Labels
FDA
EMA
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Indications
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Agency Specific
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Patent Expiration
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ATC Codes
L: Antineoplastic and immunomodulating agents
— L01: Antineoplastic agents
— L01C: Plant alkaloids and other natural products, antineoplastic drugs
— L01CA: Vinca alkaloids and analogues, antineoplastic
— L01CA05: Vinflunine
HCPCS
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Clinical
Clinical Trials
34 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
CarcinomaD002277—C80.0165—110
Transitional cell carcinomaD002295——174—110
Urinary bladder neoplasmsD001749—C67354——9
Breast neoplasmsD001943EFO_0003869C50—24——6
NeoplasmsD009369—C80411——6
Ureteral neoplasmsD014516EFO_0003844C66121——4
Neoplasm metastasisD009362EFO_0009708——12——2
Head and neck neoplasmsD006258————1——1
Squamous cell carcinoma of head and neckD000077195————1——1
Stomach neoplasmsD013274EFO_0003897C16—11——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Lung neoplasmsD008175HP_0100526C34.90—3———3
Renal insufficiencyD051437HP_0000083N1912———2
Urologic neoplasmsD014571—C64-C6811———2
Urethral neoplasmsD014523EFO_0003846—11———2
Pelvic neoplasmsD010386——11———2
Penile neoplasmsD010412—C60—1———1
Prostatic neoplasmsD011471—C61—1———1
Small cell carcinomaD018288———1———1
Small cell lung carcinomaD055752———1———1
Non-small-cell lung carcinomaD002289———1———1
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Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameVinflunine
INNvinflunine
Description
Vinflunine is an organic heteropentacyclic compound and an organic heterotetracyclic compound that is vinorelbine in which the tetrahydropyridine moiety of the heterotetracyclic part of the molecule has been redced to the corresponding piperidine, and in which the ethyl group attached to this ring has been replaced by a 1,1-difluoroethyl group. It has a role as an antineoplastic agent. It is an organic heteropentacyclic compound, an organic heterotetracyclic compound, a semisynthetic derivative, a methyl ester, an acetate ester and a vinca alkaloid. It is functionally related to a vinorelbine.
Classification
Small molecule
Drug classvinca alkaloids
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Structure (InChI/SMILES or Protein Sequence)
CC[C@]12C=CCN3CC[C@@]4(c5cc([C@@]6(C(=O)OC)C[C@@H]7C[C@@H](C(C)(F)F)CN(Cc8c6[nH]c6ccccc86)C7)c(OC)cc5N(C)[C@H]4[C@@](O)(C(=O)OC)[C@@H]1OC(C)=O)[C@@H]32
Identifiers
PDB—
CAS-ID162652-95-1
RxCUI—
ChEMBL IDCHEMBL2110725
ChEBI ID90241
PubChem CID10629256
DrugBankDB11641
UNII ID5BF646324K (ChemIDplus, GSRS)
Target
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Variants
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Financial
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Trends
PubMed Central
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Safety
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Adverse Events
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259 adverse events reported
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