Currently recruiting and recently completed trials exploring the combination of ADC and IO agents
Phase | Trial | Organ system | ADC | Antibody target | Payload (class) | IO agent (mechanism of action) | Status |
---|---|---|---|---|---|---|---|
I | NCT03523572 | Breast and urothelial | T-DXd | HER2 | DXd (DDA) | Nivo (ICI) | Recruiting (2018) |
I | NCT04042701 | NSCLC, breast | T-DXd | HER2 | DXd (DDA) | Pembrolizumab (ICI) | Recruiting (2020) |
I | NCT03364348 | Breast | T-DM1 | HER2 | DM1 (TI) | Utomilumab (CSA) | Recruiting (2017) |
I | NCT03032107 | Breast | T-DM1 | HER2 | DM1 (TI) | Pembrolizumab (ICI) | Recruiting (2017) |
II | NCT02924883 | Breast | T-DM1 | HER2 | DM1 (TI) | Atezolizumab (ICI) | Published 2021-negative trial |
I | NCT02341625 | Solid organ, mesothelioma | BMS-986148 | Mesothelin | Unknown | Nivo (ICI) | Active (2015). Not recruiting |
I | NCT03816358 | Pancreatic | Anetumab ravtansine | Mesothelin | DM4 (TI) | Nivo + ipilimumab/Nivo + chemo (ICI) | Recruiting (2019) |
I | NCT03455556 | NSCLC | Anetumab ravtansine | Mesothelin | DM4 (TI) | Atezolizumab (ICI) | Completed (2018–2020) |
I | NCT03126630 | Mesothelioma | Anetumab ravtansine | Mesothelin | DM4 (TI) | Pembrolizumab | Recruiting (2017) |
I | NCT04448886 | HR+/HER2-breast | SG | Trop-2 | SN38 (TI) | Pembrolizumab (ICI) | Recruiting (2020) |
II | NCT04468061 | TNBC | SG | Trop-2 | SN38 (TI) | Pembrolizumab | Recruiting (2020) |
Ib/II | NCT03288545 | Urothelial | EV | Nectin-4 | MMAE (TI) | Pembrolizumab (ICI) | Recruiting (2017)—FDA breakthrough designation 2019 [177] |
I | NCT03310957 | Breast | Ladiratuzumab vedotin | LIV-1 (zinc transporter subfamily) | MMAE (TI) | Pembrolizumab (ICI) | Recruiting (2018) |
I | NCT03000257 | SCLC | Rovalpituzumab tesrine | DLL3 | SC-DR002 (DDA) | Budigalimab (PD-LI) | Completed (2019) |
I/II | NCT03026166 | SCLC | Rovalpituzumab tesirine | DLL3 | SC-DR002 (DDA) | Nivo + ipilimumab (ICI) | P1 completed (2018), P2 halted (2019) due to high number of DLTs [178] |
I | NCT03639194 | SCLC | SC-011 | Unknown | DDA | ABBV-181 (ICI) | Recruiting (2018) |
I | NCT02099058 | NSCLC, solid tumours | Telisotuzumab vedotin | cMET | MMAE (TI) | Nivo | Recruiting (2014) |
I | NCT03786081 | Cervical | TV | TF | MMAE (TI) | Pembrolizumab | Recruiting (2019) |
I | NCT03729596 | Advanced solid tumours | MGC018 | Anti-B7-H3 | Unknown | MGA012 (ICI) | Recruiting (2018) |
II | NCT03835819 | Endometrial | Mirvetuximab soravtansine | FRα | DM4 (TI) | Pembrolizumab | Recruiting (2019) |
cMET: mesenchymal epithelial transition factor; CSA: co-stimulatory agent; DDA: DNA damage agent; DLL3: delta-like ligand 3; FRα: folate receptor alpha; HR+: hormone receptor positive; LIV-1: zinc transporter ZIP6/SLC39A6; Nivo: nivolumab; TI: tubulin inhibitor; +: plus
SM, SP and HKG contributed to the drafting and editing of the manuscript. SM created the figures. HKG contributed to conception and design of the review. All authors contributed to manuscript revision, read, and approved the submitted version.
The authors declare that they have no conflicts of interest.
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© The Author(s) 2022.