Drug data last refreshed 21h ago · AI intelligence enriched 2w ago
ALIMTA (pemetrexed disodium) is a folate antagonist small-molecule chemotherapy that inhibits multiple folate-dependent enzymes critical for cell replication. It is approved for non-small cell lung cancer, malignant mesothelioma, ovarian cancer, and several other solid tumors. The drug works by blocking thymidylate synthase and other nucleotide synthesis pathways, preventing tumor cell division.
Approaching loss of exclusivity with modest Part D spending signals a mature product with reduced team expansion opportunities.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Pemetrexed Disodium and Hsp90 Inhibitor AUY922 in Treating Patients With Previously Treated Stage IV Non-Small Cell Lung Cancer
TaxoteRe Plus Cisplatin Versus AlImta Plus Cisplatin in 1st Line Non-squamous Cell Type Lung Cancer
Pemetrexed Disodium/Observation in Treating Patients W/ Malignant Pleural Mesothelioma w/Out Progressive Disease After 1st Line Chemotherapy
Gemcitabine Hydrochloride or Pemetrexed Disodium and Carboplatin With or Without Celecoxib in Treating Patients With Advanced Non-Small Cell Lung Cancer
A Study of Alimta/Cisplatin/Gefitinib for Asian Non-smoking Participants With Non Small Cell Lung Cancer
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moALIMTA currently has zero linked job openings, reflecting its mature lifecycle status and declining commercial focus. Career opportunities on this product are extremely limited and concentrated in specialty pharmacy, patient support, and post-LOE generic management.