Table 4.
Clinical trials of Disitamab vedotin (DV)
| Clinical trials | Participants (cTNM/N) | Primary endpoints | Nation |
|---|---|---|---|
| DVa+PD-1 A | cT2-T4aN0-3M0/9 | 88.9% ORR [59] | China |
| DVa+PD-1 A | cT2-4bN0-3M0-1a/51 | Following [60] | China |
| DVa+PD-1 A | cT2-4aN0-2M0/11 | 81.8% ORR [61] | China |
| DVa+PD-1 A | la/mUC/185 | 62.5% ORR [55] | China |
| DVa | la/mUC/43 | 51.2% ORR [13] | China |
| DVa | la/mUC/107 | 50.5% ORR [12] | China |
| DVa vs DVa+PD-1 A | la/mUC/38 | 63.2% ORR [62] | China |
| DV vs DV+PD-1 A | la/mUC/36 | 38.9% ORR [57] | China |
PD-1 A: programmed death-1 antibody (toripalimab or tislelizumabo or pembrolizumab or envafolimab or sintilimab); la/mUC locally advanced or metastatic urothelial carcinoma
a2 mg/kg, once every 2 weeks