About this trial
The primary objective is to determine the overall response rate (ORR) of Teliso-V in subjects with c-Met-positive (c-Met+) NSCLC.
Subjects with locally advanced or metastatic NSCLC tumor cell expression that is c-Met+ per central lab immunohistochemistry (IHC) assay specification, who have previously progressed on systemic cytotoxic therapy (or ineligible), and an immune checkpoint inhibitor (as monotherapy or in combination with systemic cytotoxic chemotherapy, or ineligible) and prior anti-cancer therapies targeting driver gene alterations (if applicable) and who have received no more than 2 lines of prior systemic chemotherapy (including no more than 1 line of systemic cytotoxic chemotherapy) in the metastatic setting.
Where’s this trial being run?
St Vincents University Hospital and Mater Misericordiae University Hospital
Can I join this study / trial?
The first thing you do is to talk to your doctor and/or the cancer trials research team in your hospital. The contact details for the cancer trials research units in Ireland is here.
Why not Print this page and bring it with you. It will help your doctor and research team advise you.Print this page
For more detailed informationClick Here
Phase 2, Open-Label Safety and Efficacy Study of Telisotuzumab Vedotin (ABBV-399) in Subjects With Previously Treated c-Met+ Non-Small Cell Lung Cancer
|Principal Investigator:||Dr Emer Hanrahan (St. Vincent's University Hospital)|
Global: October 2018
Ireland: November 2019- Closing 30-Jun-2023
|Global Recruitment Target:||270|
|Ireland Recruitment Target:||9|