Table 6.
Agents
|
Targeted molecule (s)
|
Condition
|
Study phase
|
Clinical trial identifier
|
Encorafenib + Binimetinib + Cetuximab | Wild type plus BRAF V600E and MEK, EGFR | Previously untreated BRAF-mutant mCRC | Phase II | NCT03693170 |
Tucatinib + Trastuzumab | HER2 | First-line HER2-positive mCRC | Phase III | NCT05253651 |
Disitamab + Vedotin + Tislelizumab | HER2 and PD-1 | HER2-positive advanced CRC | Phase II | NCT05493683 |
Vanucizumab + Bevacizumab | VEGF-A/angiopoietin-2 and VEGF | mCRC | Phase II | NCT02141295 |
Regorafenib + Nivolumab | VEGFR1/2/3 and PD-1 | Later-lines treatment of mCRC | Phase III | NCT05328908 |
Lenvatinib + Pembrolizumab | VEGFR1/2/3 and PD-1 | mCRC | Phase III | NCT04776148 |
Fruquitinib + Camrelizumab | VEGFR tyrosine kinase and PD-1 | Non-MSI-H/dMMR mCRC | Phase II | NCT04866862 |
Disitamab + Vedotin + Pembrolizumab | HER2 and PD-1 | HER2-expressing mCRC | Phase II | NCT05333809 |
Cobimetinib + Atezolizumab | MAPK and PD-L1 | mCRC | Phase III | NCT02788279 |
Cetuximab + Vemurafenib | EGFR and mutated BRAF V600E | BRAF V600E Mutated Advanced CRC | Phase II | NCT03727763 |
Penpulimab + Anlotinib | PD-1 and VEGFR1/2/3 | Refractory mCRC | Phase II | NCT04970914 |
Favezelimab | LAG-3 and PD-1 | Previously treated metastatic PD-L1 positive CRC | Phase III | NCT05064059 |
MEN1611 + Cetuximab | PI3K and EGFR | mCRC | Phase I/II | NCT04495621 |
Encorafenib + Cetuximab + Pembrolizumab | BRAF V600E, as well as wild-type BRAF, EGFR, andPD-1 | Previously untreated mCRC | Phase II | NCT05217446 |
RXC004 + Nivolumab | Porcupine (wnt activator) and PD1 | RNF43 or RSPO aberrated, metastatic, MSS CRC after progression on SOC | Phase II | NCT04907539 |
Regorafenib + Pembrolizumab | VEGFR1/2/3PD1 | Advanced or mCRC | Phase I/II | NCT03657641 |
Isatuximab + Atezolizumab | Epitope on CD38, and PD-L1 | mCRC | Phase I/II | NCT03555149 |
Atezolizumab + Selicrelumab + Bevacizumab | PD-L1, CD40 antigen, and VEGF | mCRC | Phase I/II | NCT03555149 |
Atezolizumab + Idasanutlin | PD-L1 and MDM2 | mCRC | Phase I/II | NCT03555149 |
Atezolizumab + Regorafenib | PD-L1 andVEGFR1/2/3 | mCRC | Phase I/II | NCT03555149 |
Olaparib (MK-7339) + Bevacizumab | PARP and VEGF | Unresectable or mCRC | Phase III | NCT04456699 |
Nivolumab + Ipilimumab | PD-1 andCTLA-4 | dMMR and/or MSI mCRC resistant to anti-PD1 monotherapy | Phase II | NCT05310643 |
Nivolumab + Ipilimumab | PD-1 and CTLA-4 | dMMR and/or MSI mCRC | Phase II | NCT04730544 |
Surufatinib + Sintilimab | VEGFR1/2/3 and PD-1 | Advanced MSS-Type CRC | Phase II | NCT04764006 |
Camrelizumab + Apatinib | PD-1 and VEGFR-2 | Advanced CRC | Phase I/II | NCT04067986 |
Fruquintinib + Tislelizumab + Stereotactic ablative radiotherapy | VEGFR1/2/3 and PD-1 | mCRC | Phase II | NCT04948034 |
Avelumab + Cetuximab + mFOLFOXIRI | PD-1/PD-L1 and EGFR | Unresectable mCRC | Phase II | NCT04513951 |
Geptanolimab (GB226) + Fruquintinib | PD-1 and VEGFR1/2/3 | mCRC | Phase I | NCT03977090 |
Selinexor + Pembrolizumab | Exportin 1 and PD-1 | Previously treated mCRC with RAS mutations | Phase II | NCT04854434 |
Panitumumab + Rilotumumab | EGFR and HGF | wild-type KRAS mCRC | Phase I/II | NCT00788957 |
Panitumumab + Ganitumab | EGFR and IGF-1R | wild-type KRAS mCRC | Phase I/II | NCT00788957 |
MEK: Mitogen-activated extracellular signal-regulated kinase; EGFR: Epidermal growth factor receptor; mCRC: Metastatic colorectal cancer; HER2: Human epidermal growth factor receptor 2; PD-1: Programmed death-1; PD-L1: Programmed death ligand-1; VEGF-A: Vascular endothelial growth factor-A; VEGFR: Vascular endothelial growth factor receptor; MSI-H/dMMR: Microsatellite instability-high/mismatch repair deficient; MSS: Microsatellite stable; MAPK: mitogen-activated protein kinases; LAG-3 Lymphocyte activation gene 3; PI3K: Phosphoinositide 3-kinases; RNF43: Ring Finger Protein 43; RSPO: R-spondin; SOC: Standard of Care; PARP: Poly ADP ribose polymerase; CTLA-4: Cytotoxic T lymphocyte-associated antigen 4; HGF: Hepatocyte growth factor; IGF-1R: Insulin growth factor receptor-1.