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
Latest Information Update: 29 May 2025
At a glance
- Drugs Telisotuzumab vedotin (Primary)
- Indications Non-small cell lung cancer
- Focus Adverse reactions; Therapeutic Use
- Acronyms LUMINOSITY
- Sponsors AbbVie; AbbVie Germany
Most Recent Events
- 27 May 2025 According to AbbVie media release, data from this trial will be presented at American Society of Clinical Oncology (ASCO) Annual Meeting.
- 14 May 2025 According to an AbbVie media release, based on the data from this study, the company announced that EMRELIS (telisotuzumab vedotin-tllv) has been granted accelerated approval by the U.S. Food and Drug Administration (FDA) for the treatment of adult patients with locally advanced or metastatic, non-squamous NSCLC with high c-Met protein overexpression (OE) who have received a prior systemic therapy.
- 14 May 2025 Results presented in an AbbVie media release.