TABLE 4.
Drug (target) | Clinical trial (phase) | Status | Cancer type | Patients enrolled | Arms | Outcomes |
LY2157299 (TβRI) | NCT01220271 (Phases I/II) | Completed | Glioma | 75 | Phase I LY2157299 (160 mg) + radiotherapy + temozolamide LY2157299 (300 mg) + radiotherapy + temozolamide Phase II LY2157299 (established dose) + radiotherapy + temozolamide Radiotherapy + temozolamide |
NA |
LY3200882 (TβRI) | NCT02937272 (Phase I) | Active, not recruiting | Solid tumors | 223 | LY3200882 LY3200882 + LY3300054 LY3200882 + gemcitabine + nab-paclitaxel LY3200882 + cisplatin + radiation |
NA |
LY3200882 (TβRI) | NCT04031872 (Phases I/II) | Active, not recruiting | Colorectal metastatic cancer | 31 | Single-arm: LY3200882 + capecitabine | NA |
Cmax, maximum concentration; ORR, objective response rate; PFS, progression-free survival; CBR, clinical benefit rate; CR, complete response; PR, partial response; AUC, area under the curve; SAE, serious adverse event; OS, overall survival; NA, not available.