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.
Patient Profile
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 University Hospital Limerick
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.
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Click HereQuestions?
Here’s a list of questions you may have for your doctor or local cancer research team.
QuestionsSummary Data
| Name: | AbbVie M14-239 |
|---|---|
| Number: | 18-49 |
| Full Title: | 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) |
|---|---|
| Type: | Industry Sponsored |
| Sponsor: | AbbVie |
| Recruitment Started: |
Global: October 2018 Ireland: November 2019 |
| Global Recruitment Target: | 310 |
|---|---|
| Ireland Recruitment Target: | 9 |