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Telisotuzumab adizutecan

Generic Name
Telisotuzumab adizutecan

AbbVie's Telisotuzumab Vedotin Shows Promise in c-Met Overexpressing NSCLC

• AbbVie's telisotuzumab vedotin (Teliso-V) demonstrated a 35% overall response rate in patients with high c-Met expression in the LUMINOSITY trial. • The FDA granted breakthrough therapy designation to Teliso-V, highlighting its potential to significantly improve outcomes in NSCLC patients. • A phase 3 trial (TeliMET-NSCLC-01) is underway, comparing Teliso-V to docetaxel in c-Met-positive, non-squamous NSCLC patients. • Teliso-V targets c-Met, a protein involved in cancer progression and resistance to therapies like EGFR inhibitors, offering a novel approach.

Telisotuzumab Adizutecan Shows Promise in c-Met-Expressing Solid Tumors

• Telisotuzumab adizutecan (ABBV-400) demonstrates antitumor activity in non-small cell lung cancer (NSCLC) and gastroesophageal cancer (GEA) patients in a Phase 1 study. • In EGFR wild-type NSCLC, ABBV-400 achieved a 43.8% objective response rate (ORR) and an 85.4% clinical benefit rate at 2.4/3.0 mg/kg every three weeks. • GEA patients treated with ABBV-400 at 3.0 mg/kg every three weeks showed a 28.6% ORR and a 71.4% clinical benefit rate. • Promising initial results were observed in heavily pretreated metastatic colorectal cancer (CRC) patients with high c-Met expression, with an ORR of 37.5%.

ESMO 2024: AbbVie and Nuvalent Present Promising Data on Novel Cancer Therapies

• AbbVie presented data on mirvetuximab soravtansine for platinum-sensitive ovarian cancer, showing a 51.9% objective response rate in pre-treated patients. • Nuvalent's NVL-655 and zidesamtinib demonstrated durable responses in heavily pre-treated NSCLC patients, targeting ALK and ROS1, respectively. • AbbVie's telisotuzumab vedotin (Teliso-V) is under FDA review for accelerated approval in c-Met overexpressing non-small cell lung cancer. • Nuvalent plans to initiate a Phase 3 trial (ALKAZAR) of NVL-655 in TKI-naïve ALK-positive NSCLC patients in the first half of 2025.
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