Table 4.
Clinical trials of MV-NIS
| Therapeutic agent | Cancer type | Phase, study type | Mode of therapy | Purpose of the study | Status | Clinical trial number |
|---|---|---|---|---|---|---|
| MV-NIS | Ovarian, fallopian or peritoneal cancer | Phase 2, open-label, randomized parallel study | Intra-peritoneal administration of MV-NIS and intravenous administration of the drugs like paclitaxel or gemcitabine | Safety, tolerability and efficacy evaluation of MV-NIS in comparison with standard chemotherapy | Recruiting | NCT02364713 |
| MV-NIS in combination with cyclophosphamide | Recurrent or refractory multiple myeloma | Phase 1 and phase 2, open-label, non-randomized, parallel study | Intravenous administration of MV-NIS with cyclophosphamide | Determination of maximum tolerated dose of MV-NIS in combination with cyclophosphamide | Active, not recruiting | NCT00450814 |
| MV-NIS in combination with cyclophosphamide | Recurrent or refractory multiple myeloma | Phase 2 open-label single-group assignment | Intravenous administration of MV-NIS | Determination of the clinical efficacy of MV-NIS in combination therapy with cyclophosphamide | Recruiting | NCT02192775 |
| MV-NIS | Malignant pleural mesothelioma | Phase 1, open-label, single-group study | Intra-pleural administration of the oncolytic virus | Dose determination and safety evaluation | Active, not recruiting | NCT01503177 |
| MV-NIS | Head and Neck metastatic squamous cell carcinoma or metastatic breast cancer | Phase1, open-label, single-group study | Intra-tumoral administration of MV-NIS | Dose determination and safety evaluation | Suspended | NCT01846091 |
| MV-NIS | Unresectable or recurrent malignant peripheral nerve sheath tumor | Phase 1, single-group, open-label study | Intra-tumoral administration of MV-NIS | Dose determination and safety evaluation | Recruiting | NCT02706230 |