Emrelis (telisotuzumab vedotin-tllv)

BL 761384

Emrelis (telisotuzumab vedotin-tllv)

BL 761384

U.S. License Holder:

AbbVie Inc.

Date of License:

May-14-2025

Last Update:

June-15-2025

approved_indications FDA-Approved Indications

EMRELIS (telisotuzumab vedotin-tllv) is a c-Met-directed antibody and microtubule inhibitor conjugate 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 [greater than or equal to 50 percent of tumor cells with strong (3+) staining], as determined by an FDA-approved test, who have received a prior systemic therapy.

Methodology

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