Trial | Treatments | Patients | Method |
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De Boer, 2011 | Vandetanib plus pemetrexed (n=-9) vs. pemetrexed (n=-9) | | Sample size: -9/-9 Primary endpoint: FU duration: phase 3 |
Aisner, 2013 | vandetanib or placebo as maintenance (n=-9) vs. (n=-9) | patients with advanced non-small-cell lung cancer | Sample size: -9/-9 Primary endpoint: FU duration: phase 2 |
Ahn, 2013 | (n=-9) vs. (n=-9) | advanced or metastatic non-small-cell lung cancer following first-line platinum-doublet chemotherapy | Sample size: -9/-9 Primary endpoint: progression-free survival (PFS) rate at 3 months FU duration: phase II |
Lee ZEPHYR, 2012 | vandetanib 300 mg/d (n=617) vs. placebo (n=307) | patients with advanced non-small-cell lung cancer after prior therapy with an epidermal growth factor receptor tyrosine kinase inhibitor | Sample size: 617/307 Primary endpoint: overall survival FU duration: |
Natale, 2011 | once-daily vandetanib 300 mg (n=83) vs. gefitinib 250 mg (n=85) | patients with advanced non-small-cell lung cancer | double-blind Sample size: 83/85 Primary endpoint: FU duration: phase ii |
de Boer, 2011 | vandetanib 100 mg/d plus pemetrexed 500 mg/m(2) every 21 days (n=256) vs. placebo plus pemetrexed (n=278) | second-line treatment of advanced non-small-cell lung cancer | double-blind Sample size: 256/278 Primary endpoint: Progression-free survival (PFS) FU duration: |
Natale, 2009 | (n=-9) vs. (n=-9) | | double-blind Sample size: -9/-9 Primary endpoint: FU duration: phase ii |
Heymach, 2007 | vandetanib (100 or 300 mg/d) plus docetaxel (75 mg/m2 intravenous infusion every 21 days) (n=-9) vs. placebo plus docetaxel (n=-9) | previously treated non small-cell lung cancer | Sample size: -9/-9 Primary endpoint: FU duration: phase II |