Table 3.
Clinical trials of the adenovirus-based oncolytic viruses
| Oncolytic vector | Therapeutic agent | Cancer type | Phase, study type | Mode of therapy | Purpose of the study | Status | Clinical trial number |
|---|---|---|---|---|---|---|---|
| DNX2401 | DNX2401 in combination with temozolomide | Recurrent glioblastoma | Phase 1, open-label, single-group study | Intra-tumoral | Safety evaluation | Completed | NCT01956734 |
| DNX2401 with interferon gamma | Recurrent glioblastoma | Phase 1b, open-label, parallel assignment | Intra-tumoral | Efficacy evaluation of DNX-2401 | Completed | NCT02197169 | |
| DNX-2401 | Diffuse pontine glioma | Phase 1, open-label, single-group study | Intra-tumoral | Safety evaluation and dose determination | Recruiting | NCT03178032 | |
| DNX-2401 in combination with pembrolizumab | Recurrent glioblastoma or gliosarcoma | Phase 2, multicenter, open-label study | Intra-tumoral DNX-2401 with intravenous pembrolizumab | Single dose efficacy evaluation of DNX-2401 | Active, not recruiting | NCT02798406 | |
| ONCOS-102 | ONCOS-102 in combination with cyclophosphamide | Advance cancers, malignant solid tumor | Phase 1, open-label, single-group study | Intra-tumoral ONCOS-102 with intravenous cyclophosphamide | Safety and dosage determination | completed | NCT01598129 |
| ONCOS-102 in combination with pemetrexed/cisplatin or cyclophosphamide | Un-resectable malignant pleural mesothelioma | Randomized phase 1b or phase2 open-label, parallel group-study | Intra-tumoral ONCOS-102 | Evaluation of safety, tolerability and efficacy of ONCOS-102 in combination with chemotherapy | Active, not recruiting | NCT02879669 | |
| ONCOS-102 in combination with pembrolizumab or cyclophosphamide | Advanced or un-resectable melanoma | Phase1, open-label, single-group study | Intra-tumoral ONCOS-102 with intra-venous pembrolizumab | Safety evaluation of sequential treatment with ONCOS-102 in combination with pembrolizumab | Recruiting | NCT03003676 | |
| VCN-01 | VCN-01 in combination with gemcitabine and Abraxane | Patients with advanced solid tumors | Phase1, open-label, single-group study | Intra-venous administration of VCN-01 with gemcitabine | Safety and tolerability evaluation of VCN-01 in combination therapy | Active, not recruiting | NCT02045602 |
| VCN-01 | Refractory retinoblastoma | Phase 1, open-label, single-group study | Intra-vitreal injection of VCN-01 | Safety and efficacy evaluation | Recruiting | NCT03284268 | |
| VCN-01 in combination with durvalumab | Recurrent head and neck squamous cell carcinoma | Phase 1, multicenter, open-label, dose-escalation study | Intra-venous injection of VCN-01 and durvalumab | Safety, tolerability and efficacy evaluation | Recruiting | NCT03799744 | |
| LOAd703 | LOAd703 in combination with gemcitabine and nab-paclitaxel | Pancreatic cancer | Open-label, single-group phase 1/2 trial | Ultra-sound guided percutaneas injection of LOAd703 | Safety evaluation | Recruiting | NCT02705196 |
| LOAd703 | Pancreatic, ovarian, biliary and colorectal cancer | Open-label, single-group, phase 1/2 study | Image-guided intra-tumoral injection of LoAd703 | Evaluation of efficacy of LOAd703 in various cancers | Recruiting | NCT03225989 | |
| ColoAd1 | ColoAd1 | Resectable colon cancer, resectable non-small cell lung cancer, bladder cancer, renal cell carcinoma | Phase 1 study | Intra-tumoral injection or intravenous infusion of ColoAd1 | Mechanism of action study | Completed | NCT02053220 |
| ColoAd1 | Solid tumor of epithelial origin, colorectal cancer, bladder cancer | Phase I, Phase II study | Sub-acute fractionated intravenous injection | Dose escalation study | Completed | NCT02028442 | |
| OBP-301 | Telomelysin (OBP-301) | Esophago gastric adenocarcinoma | Phase 2 study | Intra-tumoral | Safety and efficacy study | Recruiting | NCT03921021 |
| OBP-301 and pembrolizumab | Advanced solid tumor | Phase 1 study | Intra-tumoral | Safety and efficacy study | Recruiting | NCT03172819 | |
| OBP-301 | Hepatocellular carcinoma | Phase 1 study | Intra-tumoral | Safety and efficacy study | Recruiting | NCT02293850 | |
| OBP-301 | Melanoma Stage III/IV | Phase 2 study | Intra-lesion | Safety, efficacy evaluation | Active but not recruiting | NCT03190824 | |
| CG0070 | CG0070 | Bladder cancer (BOND2) | Phase 2 study | Intra-vesical therapy | Safety and efficacy study | Completed | NCT02365818 |
| CG0070 | Bladder cancer (ExBOND) | Phase 2 study | Intra-vesical therapy | Safety and efficacy study | Withdrawn | NCT02143804 | |
| CG0070 | Carcinoma, transitional cell bladder neoplasms | Phase 1 study | Intra-vesical therapy | Evaluation of safety and dosing of CG0070 | Current recruitment status is unknown | NCT00109655 |