Form: Injection
Method of administration: Intravenous
FDA approval date: February 04, 2004
Classification: Folate Analog Metabolic Inhibitor
Summary: ALIMTA ® is a folate analog metabolic inhibitor indicated: in combination with pembrolizumab and platinum chemotherapy, for the initial treatment of patients with metastatic non-squamous NSCLC, with no EGFR or ALK genomic tumor aberrations.