Tepmetko Generic Name & Formulations
Tepotinib 225mg; tabs.
Treatment of adults with metastatic non-small cell lung cancer (NSCLC) harboring mesenchymal-epithelial transition (MET) exon 14 skipping alterations.
Tepmetko Dosage and Administration
Confirm presence of MET exon 14 skipping alterations in plasma or tumor specimens. Swallow whole. Take with food. 450mg once daily until disease progression or unacceptable toxicity. Dose modifications for adverse reactions: see full labeling.
Tepmetko Boxed Warnings
Monitor for pulmonary symptoms indicative of ILD/pneumonitis; withhold immediately if suspected and permanently discontinue if no other causes are identified. Monitor LFTs prior to initiation, every 2 weeks during 1st 3 months, then once monthly or as clinically indicated; test more frequently if increased AST, ALT or bilirubin develops. Severe renal (CrCl <30mL/min) or hepatic (Child-Pugh C) impairment. Embryo-fetal toxicity. Advise females of reproductive potential and males (w. female partners) to use effective contraception during and for 1 week after the last dose. Pregnancy: exclude status prior to initiation. Nursing mothers: not recommended (during and for 1 week after the last dose).
May be potentiated by dual strong CYP3A and P-gp inhibitors; avoid. May be antagonized by strong CYP3A inducers; avoid. Potentiates certain P-gp substrates (eg, dabigatran etexilate); if unavoidable, reduce substrate dosage.
Tepmetko Adverse Reactions
Edema, fatigue, nausea, diarrhea, musculoskeletal pain, dyspnea; Grade 3 or 4 lab abnormalities (decreased lymphocytes, decreased albumin, decreased sodium, increased GGT, increased amylase, increased ALT/AST, decreased hemoglobin); hepatotoxicity.
Tepmetko Clinical Trials
Tepmetko Patient Counseling