Lomustine
Gleostine (lomustine) is a small molecule pharmaceutical. Lomustine was first approved as Gleostine on 1982-01-01. It is used to treat brain neoplasms, colonic neoplasms, hodgkin disease, kidney neoplasms, and lung neoplasms amongst others in the USA.
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Commercial
Trade Name
FDA
EMA
Gleostine
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Lomustine
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
GLEOSTINE | CordenPharma | N-017588 RX | 1982-01-01 | 3 products, RLD, RS |
Show 1 discontinued
Labels
FDA
EMA
Brand Name | Status | Last Update |
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gleostine | New Drug Application | 2020-11-10 |
Agency Specific
FDA
EMA
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Patent Expiration
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HCPCS
Code | Description |
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S0178 | Lomustine, oral, 10 mg |
Clinical
Indications Phases 4
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Indications Phases 3
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Indications Phases 2
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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 name | LOMUSTINE |
INN | lomustine |
Description | Lomustine is an N-nitrosourea that is urea in which one of the nitrogens is substituted by a 2-chloroethyl group and by a nitroso group, while the other nitrogen is substituted by a cyclohexyl group. An alkylating antineoplastic agent, it is used in the treatment of brain tumours, lung cancer, malignant melanoma and other solid tumours. It has a role as an alkylating agent and an antineoplastic agent. It is a member of N-nitrosoureas and an organochlorine compound. |
Classification | Small molecule |
Drug class | antineoplastics (chloroethylamine derivatives) |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | O=NN(CCCl)C(=O)NC1CCCCC1 |
Identifiers
PDB | — |
CAS-ID | 13010-47-4 |
RxCUI | 6466 |
ChEMBL ID | CHEMBL514 |
ChEBI ID | 6520 |
PubChem CID | 3950 |
DrugBank | DB01206 |
UNII ID | 7BRF0Z81KG (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
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Financial
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Trends
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Safety
Black-box Warning
Black-box warning for: Gleostine
Adverse Events
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152 adverse events reported
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