Table 2.
Year | Targeted Therapy | Antiangiogenic Therapy | Phase | Status | Results | ClinicalTrials.gov identifier |
---|---|---|---|---|---|---|
2008 | Tandutinib (ems-like tyrosine kinase 3 antagonist) | Bevacizumab | II | Completed | Primary endpoint: six-month progression-free survival was 23%. Tandutinib with bevacizumab was equally effective but more toxic than bevacizumab monotherapy. |
NCT00667394 (152) |
2008 | Everolimus (mTOR inhibitor) | Bevacizumab | II | Completed | Primary endpoint: median progression free survival was 11.3 months. | NCT00805961 (153) |
2008 | Temsirolimus (mTOR inhibitor) | Bevacizumab | II | Completed | Primary endpoint: median progression free survival of eight weeks. Trial terminated early because of poor outcomes. | NCT00800917 (153) |
2011 | Buparlisib (selective PI3K inhibitor) | Bevacizumab | I/II | Completed | Primary endpoint: median progression free survival was 5.3 months. Full results not published. |
NCT01349660 (41) |
2011 | Plerixafor (CXCR4 inhibitor) | Bevacizumab | I | Terminated | n/a | NCT01339039 |
2015 | Ofranergene obadenovec (adenovirus delivering chimeric death receptor | Ofranergene obadenovec/ Bevacizumab |
III | Completed | Primary endpoint: median overall survival was 6.8 months in combination arm versus 7.9 months in control arm. Change of treatment regimen, with the lack of VB-111 monotherapy priming, may explain the differences from the favorable phase II results. |
NCT02511405 (135) |
2018 | ABI009 - nanoparticle albumin-bound rapamycin (mTOR inhibitor) | Bevacizumab | II | Active, not recruiting | Ongoing | NCT03463265 |
2019 | Abemaciclib (CDK 4/6 inhibitors) | Bevacizumab | I | Recruiting | Ongoing | NCT04074785 |