Table 3.
Company | Target | Linker | Payload | MM cell EC50* |
Pros | Cons | Trial status | |
---|---|---|---|---|---|---|---|---|
Indatuximab Ravtansine |
Biotest | CD138 | Cleavable | DM4 | 1 nM | Good target cell specificity | Internalization efficiency unknown |
Phase I/Iia (open) |
Lorvotuzumab mertansine |
ImmunoGen | CD56 | Cleavable | DM1 | 10–50 nM | Upregulated expression on MM cells |
Expression on other cell types |
Development discontinued |
Milatuzumab–DOX | Immunomedics | CD74 | Acid labile hydrazone |
Doxorubicin | 900 nM | Rapid internalization and recycling |
Lower potency, labile linker |
Phase I (not open) |
anti-FcrL5 ADC | Genetech | FcrL5 | Cleavable & non- cleavable |
DM4, MMAF and MMAE |
0.33 nM | High target cell specificity | Low expression level? | Not yet registered |
GSK2857916 | GlaxoSmith Kline |
BCMA | Non-cleavable | MMAF | 0.08–6.6 nM | High target cell specificity | Variable expression level |
Phase I (not open) |
Cross-comparison of agent EC50s is limited due to varying assay conditions and cell lines used in the study.