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Telisotuzumab Vedotin · Emrelis, ABBV-399

Antibody-drug conjugate · Cytotoxic, directed at c-Met (MET) · developed by Abbvie

Approved FDA, May 2025
ABBV Developer
1 Registered trials

What is Telisotuzumab Vedotin?

Telisotuzumab vedotin-tllv is a c-Met-directed antibody drug conjugate containing MMAE, a microtubule-disrupting agent. The antibody binds c-Met on tumor cells, undergoes internalization, and releases MMAE intracellularly to disrupt microtubules, causing cell cycle arrest and apoptosis.

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as
Emrelis, ABBV-399, ABT-399, PR-1420682
Drug type
Antibody-drug conjugate
Targets
c-Met (MET)
Mechanism
Cytotoxic, directed at c-Met (MET)
Pathways
microtubule disruption, cell cycle arrest, apoptosis
Therapy area
Oncology
Developer
Abbvie Inc (ABBV)
FDA status
Approved as Emrelis (May 14, 2025), BLA761384 · FDA label
UNII
976X9VXC3Z

✅ FDA-approved uses

From the indications section of the FDA label (version of May 25, 2025). Read the full label for the exact wording, limitations and safety information.

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT04928846 Phase 3 Non Small Cell Lung Cancer Recruiting ABBV

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Non Small Cell Lung Cancer

Other drugs acting on MET

More from Abbvie

Sources

Updated Oct 3, 2026. Something wrong or missing? Report it on the ABBV page.

Follow ABBV, the company behind Telisotuzumab Vedotin

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Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.