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Drug ReportsPemetrexed
Alimta(pemetrexed)
Alimta, Armisarte, Ciambra, Pemetrexed, Pemfexy (pemetrexed) is a small molecule pharmaceutical. Pemetrexed was first approved as Alimta on 2004-02-04. It is used to treat mesothelial neoplasms and non-small-cell lung carcinoma in the USA. It has been approved in Europe to treat mesothelioma and non-small-cell lung carcinoma. The pharmaceutical is active against dihydrofolate reductase. In addition, it is known to target proton-coupled folate transporter, thymidylate synthase, and trifunctional purine biosynthetic protein adenosine-3.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
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FDA approval date
EMA approval date
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Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
neoplasmsD009369
respiratory tract diseasesD012140
Trade Name
FDA
EMA
Alimta, Pemetrexed, Pemetrexed ditromethamine, Pemfexy (discontinued: Pemetrexed, Pemetrexed ditromethamine)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Pemetrexed disodium
Tradename
Company
Number
Date
Products
PEMETREXED DISODIUMAccord HealthcareN-214408 RX2022-07-19
4 products, RLD, RS
PEMETREXED DISODIUMHospiraN-214218 RX2022-06-22
3 products, RLD, RS
ALIMTAEli LillyN-021462 RX2004-02-04
2 products, RLD, RS
PEMETREXED DISODIUMSandozN-214657 RX2022-05-26
3 products, RLD, RS
PEMETREXEDShilpa MedicareN-215179 RX2023-05-22
3 products, RLD, RS
Pemetrexed
Tradename
Company
Number
Date
Products
PEMETREXEDAllerganN-208419 RX2020-08-21
3 products, RLD, RS
PEMFEXYEagle PharmaceuticalsN-209472 RX2020-02-08
1 products, RLD, RS
Pemetrexed ditromethamine
Tradename
Company
Number
Date
Products
PEMETREXED DITROMETHAMINEHospiraN-208746 RX2022-06-10
2 products, RLD, RS
Show 1 discontinued
Labels
FDA
EMA
Brand Name
Status
Last Update
alimtaNew Drug Application2023-05-19
axtleNew Drug Application2024-12-27
pemetrexedNew Drug Application2024-11-28
pemetrexed disodiumANDA2022-11-15
pemfexyNew Drug Application2023-05-15
pemrydi rtuNew Drug Application2024-11-11
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
non-small-cell lung carcinoma—D002289—
mesothelial neoplasms—D018301—
Agency Specific
FDA
EMA
No data
Patent Expiration
Patent
Expires
Flag
FDA Information
Pemetrexed, Pemfexy, Eagle Pharms
96049902035-10-28DP
Pemetrexed Disodium, Pemetrexed, Shilpa
111478172035-03-26DP
ATC Codes
L: Antineoplastic and immunomodulating agents
— L01: Antineoplastic agents
— L01B: Antimetabolites
— L01BA: Folic acid analogs, antimetabolites
— L01BA04: Pemetrexed
HCPCS
Code
Description
J9304
Injection, pemetrexed (pemfexy), 10 mg
J9305
Injection, pemetrexed, not otherwise specified, 10 mg
Clinical
Clinical Trials
1301 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Non-small-cell lung carcinomaD002289————1——1
Indications Phases 2
No data
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common namePemetrexed
INNpemetrexed
Description
Pemetrexed, sold under the brand name Alimta among others, is a chemotherapy medication for the treatment of pleural mesothelioma and non-small cell lung cancer (NSCLC)..
Classification
Small molecule
Drug classantineoplastic thymidylate synthetase inhibitors
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Structure (InChI/SMILES or Protein Sequence)
Nc1nc2[nH]cc(CCc3ccc(C(=O)N[C@@H](CCC(=O)O)C(=O)O)cc3)c2c(=O)[nH]1
Identifiers
PDB—
CAS-ID137281-23-3
RxCUI—
ChEMBL IDCHEMBL225072
ChEBI ID63616
PubChem CID446556
DrugBankDB00642
UNII ID04Q9AIZ7NO (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
Alimta – Eli Lilly
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Pemfexy – Eagle Pharmaceuticals
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Tabular view
Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 23,214 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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30,868 adverse events reported
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