| Revision as of 12:43, 16 August 2006 editAndrew73 (talk | contribs)Extended confirmed users3,990 edits reverted vandalism← Previous edit | Revision as of 16:17, 18 August 2006 edit undoPhil E.Stein (talk | contribs)8 edits revert to 83Next edit → | ||
| Line 11: | Line 11: | ||
| In ], the ] approved pemetrexed for treatment of malignant ]l ], a type of tumor of the lining of the lung, in combination with ]. In ], the FDA granted approval as a second-line agent for the treatment of non-small cell ]. | In ], the ] approved pemetrexed for treatment of malignant ]l ], a type of tumor of the lining of the lung, in combination with ]. In ], the FDA granted approval as a second-line agent for the treatment of non-small cell ]. | ||
| Patients are required to be on ] and vitamin ] supplementation when they are on pemetrexed therapy. (In clinical trials for mesothelioma, folic acid and B12 supplementation reduced the frequency of adverse events.) It is also recommended for patients to be on a steroid (e.g. ] 4mg twice daily) on the day prior, day of, and day after pemetrexed infusion to avoid skin rashes. | Patients are required to be on ] and vitamin ] supplementation when they are on pemetrexed therapy. (In clinical trials for mesothelioma, folic acid and B12 supplementation reduced the frequency of adverse events.) It is also recommended for patients to be on a steroid (e.g. ] 4mg twice daily) on the day prior, day of, and day after pemetrexed infusion to avoid skin rashes .. | ||
| ==External links== | ==External links== | ||
Revision as of 16:17, 18 August 2006
Pharmaceutical compound| File:Pemetrexed.jpg | |
| Clinical data | |
|---|---|
| Routes of administration | IV |
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Bioavailability | NA |
| Protein binding | 81% |
| Metabolism | Negligible |
| Elimination half-life | 3.5 hours |
| Excretion | Renal |
| Identifiers | |
IUPAC name
| |
| CAS Number | |
| PubChem CID | |
| DrugBank | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.205.735  |
| Chemical and physical data | |
| Formula | C20H21N5O6 |
| Molar mass | 427.411 g/mol g·mol |
Pemetrexed (brand name Alimta®) is a chemotherapy drug. Its indications are the treatment of pleural mesothelioma as well as non-small cell lung cancer.
History
The molecular structure of pemetrexed was developed by Edward C. Taylor at Princeton University and clinically developed by Indianapolis based drug maker, Eli Lilly and Company.
Mechanism of action
Pemetrexed is chemically similar to folic acid and is in the class of chemotherapy drugs called folate antimetabolites. It works by inhibiting three enzymes used in purine and pyrimidine synthesis—thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyl transferase (GARFT). By inhibiting the formation of precursor purine and pyrimidine nucleotides, pemetrexed prevents the formation of DNA and RNA, which are required for the growth and survival of both normal cells and cancer cells.
Clinical use
In February 2004, the Food and Drug Administration approved pemetrexed for treatment of malignant pleural mesothelioma, a type of tumor of the lining of the lung, in combination with cisplatin. In July 2004, the FDA granted approval as a second-line agent for the treatment of non-small cell lung cancer.
Patients are required to be on folic acid and vitamin B12 supplementation when they are on pemetrexed therapy. (In clinical trials for mesothelioma, folic acid and B12 supplementation reduced the frequency of adverse events.) It is also recommended for patients to be on a steroid (e.g. dexamethasone 4mg twice daily) on the day prior, day of, and day after pemetrexed infusion to avoid skin rashes ..
External links
 | This pharmacology-related article is a stub. You can help Misplaced Pages by expanding it. |