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 |