Condition: Renal Cell Carcinoma · Sponsor: AVEO Pharmaceuticals, Inc.
Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
This study will be comparing tivozanib in combination with nivolumab to tivozanib alone in subjects with advanced Renal Cell Carcinoma (RCC) who have had 1 or 2 prior lines of therapy, one of which was an Immune Checkpoint Inhibitor (ICI).
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Inclusion Criteria: * Radiographic disease progression during or following at least 6 weeks of treatment with ICI for locally advanced or metastatic RCC with a clear cell component either in first- or second-line treatment. * Subjects must have recovered from the adverse events of prior therapy to grade ≤ 1 or baseline. * Histologically or cytologically confirmed RCC with a clear cell component. * Measurable disease per RECIST criteria Version 1.1. * Eastern Cooperative Oncology Group performance status of 0 or 1. * All participants must follow protocol defined contraceptive measures. Exclusion Criteria: * Subjects who received: a. A single agent tyrosine kinase inhibitor (TKI) in the first line setting followed by a single agent immune checkpoint inhibitor (ICI) in the second line setting; b. More than 2 prior lines of therapy in the advanced or metastatic setting. * History of life-threatening toxicity related to prior immune therapy. * Active autoimmune disease as well as those that required discontinuation of prior immuno-oncological (IO) therapy due to immune mediated AEs. * Uncontrolled hypertension. * More than 1 prior line of therapy with a checkpoint inhibitor in the metastatic setting. * Subjects on immune suppressive therapy for organ transplant or subjects with a history of genetic or acquired immune suppression disease such as human immunodeficiency virus (HIV) \[Patients with HIV who have CD4+ T-cell counts \>350 cells/µL, without a history of acquired immune deficiency syndrome (AIDS)-defining opportunistic infections, and are on established antiretroviral therapy which does not include a cytochrome P450 (CYP)3A4 inducer, for at least 4 weeks and have an HIV viral load less than 400 copies/mL, are eligible\]. * History of clinically significant interstitial lung disease or current non-infectious pneumonitis.
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| City of Hope Comprehensive Cancer Center | Duarte, California, United States | — |
| Chao Family Comprehensive Cancer Center, UC Irvine | Irvine, California, United States | — |
| University of California San Diego | La Jolla, California, United States | — |
| Leland Stanford Junior University | Redwood City, California, United States | — |
| Kaiser Permanente Riverside Medical Center | Riverside, California, United States | — |
| US Oncology - Rocky Mountain Cancer Centers - Midtown | Denver, Colorado, United States | — |
| Florida Cancer Specialists & Res Inst | Fort Myers, Florida, United States | — |
| Florida Cancer Specialists & Research Institute (FCS) - Tampa Cancer Center Location | St. Petersburg, Florida, United States | — |
| The University of Kansas Cancer Center | Westwood, Kansas, United States | — |
| University of Kentucky UK Markey Cancer Center | Lexington, Kentucky, United States | — |
| Tulane Cancer Center Clinic - Oncology | New Orleans, Louisiana, United States | — |
| University of Maryland Medical Center-Greenebaum Cancer Ctr | Baltimore, Maryland, United States | — |
+ 127 more locations — full list on the registry record.
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