Telisotuzumab Vedotin: Side Effects, Uses & Monitoring

Facts extracted from current FDA product labeling for Telisotuzumab Vedotin. Educational only — not medical advice.

Labeled uses

EMRELIS is indicated for the treatment of adult patients with locally advanced or metastatic, non-squamous non-small cell lung cancer (NSCLC) with high c-Met protein overexpression [≥50% of tumor cells with strong (3+) staining], as determined by an FDA-approved test [see Dosage and Administration ( 2.1 )] , who have received a prior systemic therapy. This indication is approved under accelerated approval based on overall response rate (ORR) and duration of response  (DOR) [see Clinical Studies ( 14 )] . Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).

Source: FDA labeling via NIH DailyMed (set bc04f980…). Not affiliated with FDA or NIH.

Medical disclaimer: Always consult a qualified healthcare professional about any medication.