OnCo
trialsTrialRecruiting

TeliMET NSCLC-01

The confirmatory trial for the first c-MET ADC, which was approved early on response rate alone.

Randomised phase 3 to confirm the May 2025 accelerated approval (LUMINOSITY ORR ~35% in c-Met high). Enrolment ongoing.

Setting
Previously treated c-Met-overexpressing, EGFR-wild-type non-squamous NSCLC: telisotuzumab vedotin vs docetaxel
Phase
Phase 3
Sponsor
AbbVie
Registry
Enrolled
698
Replication
Ongoing confirmatory trial for the LUMINOSITY-based accelerated approval.

Connected

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