Browse By Model Organism Result Page of OvirusTdb

The total number of records retrieved from this search are 100. Click on ID to see further detail.
IDOV_192Virus nameHerpes simplex virusVirus strainrQNestin34.5Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationDeletion mutant for both copies of gamma 34.5 gene and ICP6 gene, re-addition of 34.5 gene under nestin promoterVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic nu/nu mice injected intracranially with GBM30 cells 1.0E+5 cellsIn-vivo virus concentration5.0E+5 PFU (on 5 day) in total 8 miceIn-vivo toxicityNA In-vivo result40% mice survived on 28th dayMode of deliveryIntratumorallyPathway inducedNAImmunogenic effectNAClinical trialNAPMID26524593
IDOV_193Virus nameHerpes simplex virusVirus strainrQNestin34.5Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationDeletion mutant for both copies of gamma 34.5 gene and ICP6 gene, re-addition of 34.5 gene under nestin promoterVirus aloneNoVirus in combination with drug/radiationVirus in combination with tubastatin A (TA) at a dose of 1.3 mg per kg body weight (4, 5, 6, 7 and 8 days after tumor implantation)Immune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic nu/nu mice injected intracranially with GBM30 cells 1.0E+5 cellsIn-vivo virus concentration5.0E+5 PFU (on 5 day) in total 8 miceIn-vivo toxicityNA In-vivo result80% mice survived on 28th dayMode of deliveryIntratumorallyPathway inducedNAImmunogenic effectNAClinical trialNAPMID26524593
IDOV_357Virus nameAdenovirusVirus strainAdhz60Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationE1b-deleted mutantVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic BALB/c nu/nu male mice (subcutaneously injected A549 lung cancer cells, 5.0E+6 cells)In-vivo virus concentration1.0E+9 pfu (every 3 days for at total 4 treatments)In-vivo toxicityNA In-vivo result41% smaller tumor size compared to the negative control virus AdLacZMode of deliveryIntratumorallyPathway inducedNAImmunogenic effectNAClinical trialNAPMID26561948
IDOV_358Virus nameAdenovirusVirus strainAdhz60Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationE1b-deleted mutantVirus aloneNoVirus in combination with drug/radiationVirus in combination with temozolomide (TMZ) intraperitoneally at 50 mg/Kg for five consecutive daysImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic BALB/c nu/nu male mice (subcutaneously injected A549 lung cancer cells, 5.0E+6 cells)In-vivo virus concentration1.0E+9 pfu (every 3 days for at total 4 treatments)In-vivo toxicityNA In-vivo result70% smaller tumor size compared to the negative control virus AdLacZMode of deliveryIntratumorallyPathway inducedJNK activation induces autophagyImmunogenic effectNAClinical trialNAPMID26561948
IDOV_359Virus nameAdenovirusVirus strainAdLacZVirus genome typeDNAVirus familyAdenoviridaeVirus genome modificationE1/E3-deleted mutantVirus aloneNoVirus in combination with drug/radiationVirus in combination with temozolomide (TMZ) intraperitoneally at 50 mg/Kg for five consecutive daysImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic BALB/c nu/nu male mice (subcutaneously injected A549 lung cancer cells, 5.0E+6 cells)In-vivo virus concentration1.0E+9 pfu (every 3 days for at total 4 treatments)In-vivo toxicityNA In-vivo result30% smaller tumor size compared to the negative control virus AdLacZMode of deliveryIntratumorallyPathway inducedJNK activation induces autophagyImmunogenic effectNAClinical trialNAPMID26561948
IDOV_376Virus nameHerpes simplex virusVirus strainSeprehvir (HSV1716)Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationΔγ134.5 attenuated virus mutantVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice (subcutaneously xenografted with CHLA-20)In-vivo virus concentration1.0E+7 pfu in 100 μL (on days 0, 2 and 4 after the tumor mass reached 150–300 mm³)In-vivo toxicityNA In-vivo result42% mice survivedMode of deliveryIntratumorallyPathway inducedNAImmunogenic effectNAClinical trialNAPMID26583803
IDOV_377Virus nameHerpes simplex virusVirus strainSeprehvir (HSV1716)Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationΔγ134.5 attenuated virus mutantVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice (subcutaneously xenografted with CHP-123)In-vivo virus concentration1.0E+7 pfu in 100 μL (on days 0, 2 and 4 after the tumor mass reached 150–300 mm³)In-vivo toxicityNA In-vivo result63% mice survivedMode of deliveryIntratumorallyPathway inducedNAImmunogenic effectNAClinical trialNAPMID26583803
IDOV_378Virus nameHerpes simplex virusVirus strainSeprehvir (HSV1716)Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationΔγ134.5 attenuated virus mutantVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice (subcutaneously xenografted with SK-N-AS)In-vivo virus concentration1.0E+7 pfu in 100 μL (on days 0, 2 and 4 after the tumor mass reached 150–300 mm³)In-vivo toxicityNA In-vivo result0% mice survivedMode of deliveryIntratumorallyPathway inducedNAImmunogenic effectNAClinical trialNAPMID26583803
IDOV_379Virus nameHerpes simplex virusVirus strainSeprehvir (HSV1716)Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationΔγ134.5 attenuated virus mutantVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice (subcutaneously xenografted with SK-N-BE(2))In-vivo virus concentration1.0E+7 pfu in 100 μL (on days 0, 2 and 4 after the tumor mass reached 150–300 mm³)In-vivo toxicityNA In-vivo result18% mice survivedMode of deliveryIntratumorallyPathway inducedNAImmunogenic effectNAClinical trialNAPMID26583803
IDOV_392Virus nameVaccinia virusVirus strainGLV-1h68Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHomozygous athymic female nude mice (subcutaneously injected with KMC-1 cells suspended in 50 μl Matrigel)In-vivo virus concentration1.0E+7 PFUIn-vivo toxicityNA In-vivo resultReduction in tumor volume to 30 cubic millimeter compared to control 200 cubic millimeter after 15 daysMode of deliveryIntratumorallyPathway inducedNAImmunogenic effectNAClinical trialNAPMID26584530
IDOV_749Virus nameAdenovirusVirus strainAdAFPp-E1AVirus genome typeDNAVirus familyAdenoviridaeVirus genome modificationThe viral mutant with E1A gene driven by AFP promoterVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHepG2 orthotopic liver xenograft tumor in Balb/c athymic nudeIn-vivo virus concentrationNAIn-vivo toxicityNA In-vivo resultReduction in tumor weight to 0.2 g compared to control 0.75 g after 18 daysMode of deliveryintravenouslyPathway inducedNAImmunogenic effectNAClinical trialNAPMID27450327
IDOV_750Virus nameAdenovirusVirus strainAdAFPp-E1A-122Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationThe viral insertion mutant with miR-122 target sequence into AdAFPp-E1A for negatively regulating E1A gene expressionVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHepG2 orthotopic liver xenograft tumor in Balb/c athymic nudeIn-vivo virus concentrationNAIn-vivo toxicityNA In-vivo resultReduction in tumor weight to 0.2 g compared to control 0.75 g after 18 daysMode of deliveryintravenouslyPathway inducedNAImmunogenic effectNAClinical trialNAPMID27450327
IDOV_751Virus nameAdenovirusVirus strainAdTrackVirus genome typeDNAVirus familyAdenoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHepG2 orthotopic liver xenograft tumor in Balb/c athymic nudeIn-vivo virus concentrationNAIn-vivo toxicityNA In-vivo resultReduction in tumor weight to 0.85 g compared to control 0.75 g after 18 daysMode of deliveryintravenouslyPathway inducedNAImmunogenic effectNAClinical trialNAPMID27450327
IDOV_752Virus nameAdenovirusVirus strainAdAFPp-E1A-122Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationThe viral insertion mutant with miR-122 target sequence into AdAFPp-E1A for negatively regulating E1A gene expressionVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHepG2 subcutaneous liver xenograft tumor in Balb/c athymic nudeIn-vivo virus concentrationNAIn-vivo toxicityNA In-vivo resultReduction in tumor volume to 0.8 cubic centimeter compared to control 2.4 cubic centimeter after 15 daysMode of deliveryintravenouslyPathway inducedNAImmunogenic effectNAClinical trialNAPMID27450327
IDOV_838Virus nameHerpes simplex virusVirus strainHSV-G207Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationDeletion mutant of both copies of gamma 34.5 geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic rat xenograft model for C85 cell lineIn-vivo virus concentration1.0E+7 pfu In-vivo toxicityNA In-vivo resultNo responseMode of deliveryDirect injectionPathway inducedNAImmunogenic effectNAClinical trialNAPMID10428757
IDOV_839Virus nameHerpes simplex virusVirus strainHSV-G207Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationDeletion mutant of both copies of gamma 34.5 geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic rat xenograft model for C86 cell lineIn-vivo virus concentration1.0E+7 pfu In-vivo toxicityNA In-vivo result4 xenograft model shows partial reduction and 2 shows complete reduction (50% reduction)Mode of deliveryDirect injectionPathway inducedNAImmunogenic effectNAClinical trialNAPMID10428757
IDOV_840Virus nameHerpes simplex virusVirus strainHSV-G207Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationDeletion mutant of both copies of gamma 34.5 geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic rat xenograft model for HCT8 cell lineIn-vivo virus concentration1.0E+7 pfu In-vivo toxicityNA In-vivo result4 xenograft model shows complete reduction and 4 shows partial reduction (complete reduction)Mode of deliveryDirect injectionPathway inducedNAImmunogenic effectNAClinical trialNAPMID10428757
IDOV_858Virus nameMeasles virusVirus strainMV-EdmVirus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationRecombinant expressing a peptideVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomevirus expressing a marker peptide (MV-hCEA)Source of cell lineNaturalOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic mouse xenograft model for SKOV3 cell lineIn-vivo virus concentration1.0E+7 pfu/mlIn-vivo toxicityNA In-vivo resultMedian survival time increased by >105 daysMode of deliverysubcutaneousPathway inducedNAImmunogenic effectNAClinical trialNAPMID12183422
IDOV_859Virus nameMeasles virusVirus strainMV-EdmVirus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationRecombinant expressing a peptideVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomevirus expressing a marker peptide (MV-hCEA)Source of cell lineNaturalOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic mouse xenograft model for SKOV3 cell lineIn-vivo virus concentration10⁷pfu/mlIn-vivo toxicityNA In-vivo resultMedian survival time increased by >80 daysMode of deliveryintraperitonialPathway inducedNAImmunogenic effectNAClinical trialNAPMID12183422
IDOV_897Virus nameHerpes simplex virusVirus strainMutantVirus genome typeDNAVirus familyHerpesviridaeVirus genome modificationDeletion mutant for Gamma 34.5Virus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd athymic nude mice xenograft for Hep 3B cancer cell lineIn-vivo virus concentration1.0E+7 pfu In-vivo toxicityNA In-vivo resultComplete reduction in tumor nodes after 4 weeksMode of deliveryintraperitonialPathway inducedNAImmunogenic effectNAClinical trialNAPMID12788648
IDOV_1103Virus nameAdenovirusVirus strainZD55-IL-24Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationAdenovirus expressing ZD55 gene and IL-24 geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeExpressing IL-24 geneSource of cell lineShanghai cell collectionOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic BALB/c nude mice xenograft for SW620 cell lineIn-vivo virus concentration5.0E+8 cells per wellIn-vivo toxicityNA In-vivo resultDecrease in tumor volume below 800mm³ as compared to controlMode of deliveryIntratumoral injectionPathway inducedApoptosis induction and cspase 3 activationImmunogenic effectNAClinical trialNAPMID15661558
IDOV_1104Virus nameAdenovirusVirus strainAd-IL-24Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationAdenovirus expressing IL-24 geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeExpressing IL-24 geneSource of cell lineShanghai cell collectionOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic BALB/c nude mice xenograft for SW620 cell lineIn-vivo virus concentration5.0E+8 cells per wellIn-vivo toxicityNA In-vivo resultDecrease in tumor volume below 600mm³ as compared to controlMode of deliveryIntratumoral injectionPathway inducedApoptosis induction and cspase 3 activationImmunogenic effectNAClinical trialNAPMID15661558
IDOV_1105Virus nameAdenovirusVirus strainONYX-015Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineShanghai cell collectionOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic BALB/c nude mice xenograft for SW620 cell lineIn-vivo virus concentration5.0E+8 cells per wellIn-vivo toxicityNA In-vivo resultComplete reduction in tumor volumeMode of deliveryIntratumoral injectionPathway inducedApoptosis induction and cspase 3 activationImmunogenic effectNAClinical trialNAPMID15661558
IDOV_1190Virus nameAdenovirusVirus strainICOVIR-5Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationNoneVirus aloneNoVirus in combination with drug/radiationICOVIR-5 in combination with RAD001 drug (5mg/kg for 5 days)Immune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman glioblastoma cell lineCell lineU-87 MGConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for U87MG cellsIn-vivo virus concentration1.0E+7 pfu In-vivo toxicityNA In-vivo resultComplete reduction of tumor after 90 days in 20-40% of animalsMode of deliveryNAPathway inducedNAImmunogenic effectNAClinical trialNAPMID17557108
IDOV_1191Virus nameAdenovirusVirus strainICOVIR-5Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationNoneVirus aloneNoVirus in combination with drug/radiationICOVIR-5 in combination with Temozolomide drug (7.5mg/kg for 5 days)Immune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman glioblastoma cell lineCell lineU-87 MGConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for U87MG cellsIn-vivo virus concentration1.0E+7 pfu In-vivo toxicityNA In-vivo resultComplete reduction of tumor after 90 days in 20-40% of animalsMode of deliveryNAPathway inducedNAImmunogenic effectNAClinical trialNAPMID17557108
IDOV_1665Virus nameHerpes simplex virusVirus strainHSV-1Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeVirus expressing vstat120 geneSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice, injected with U87deltaEGFR cell lineIn-vivo virus concentration1.0E+5 pfuIn-vivo toxicityNA In-vivo resultSignificant increase in median survival time of miceMode of deliveryIntracranialPathway inducedNAImmunogenic effectNAClinical trialNAPMID19844198
IDOV_1666Virus nameHerpes simplex virusVirus strainHSV-1Virus genome typeDNAVirus familyHerpesviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeVirus expressing vstat120 geneSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice, injected with GlideltaEGFR-H2B-RFP cell lineIn-vivo virus concentration1.5E+6 cellsIn-vivo toxicityNA In-vivo resultSignificant reduction in tumor volume and increase in median survival time of miceMode of deliverySubcutaneouslyPathway inducedNAImmunogenic effectNAClinical trialNAPMID19844198
IDOV_1915Virus nameVaccinia virusVirus strainGLV-1h68Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineMalignan small cell canine carcinoma cell lineCell lineMTH52cConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd athymic nude mice xenograft for MTH52c cell lineIn-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultSignificant decrease in tumor volume after 42 daysMode of deliveryNAPathway inducedNAImmunogenic effectVirus cause increase expression of ApoA1, IL-2,11,18,IFN-gamma, IP-10, MCP-1,3,5,MIP-2,MMP-9 and TNF alphaClinical trialNAPMID20631910
IDOV_2063Virus nameVaccinia virusVirus strainGLV-1h68Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman hepatocellular carcinoma cell lineCell linePLCConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic hsd nude mice xenograft for PLC cell lineIn-vivo virus concentration5.0E+6 pfuIn-vivo toxicityReduction in tumor volume below 2000mm compared to control after 45 days In-vivo resultNo responseMode of deliveryNAPathway inducedInduction of apoptosis in cancer cell lineImmunogenic effectIncreased expression of immunological gene such as GM-CSF, IFN-gamma, IL-6,2,12,18, IP-10, MCP-1,3,5, TNF-alpha and MIP-2Clinical trialNAPMID21779374
IDOV_2064Virus nameVaccinia virusVirus strainGLV-1h68Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman hepatocellular carcinoma cell lineCell lineHuh-7Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic hsd nude mice xenograft for PLC cell lineIn-vivo virus concentration5.0E+6 pfuIn-vivo toxicityReduction in tumor volume below 3000mm compared to control after 35 days In-vivo resultMode of deliveryNAPathway inducedInduction of apoptosis in cancer cell lineImmunogenic effectIncreased expression of immunological gene such as GM-CSF, IFN-gamma, IL-6,2,12,18, IP-10, MCP-1,3,5, TNF-alpha and MIP-2Clinical trialNAPMID21779374
IDOV_2408Virus nameVesicular stomatitis virusVirus strainVSV-Delta-M51-GFPVirus genome typeRNAVirus familyRhabdoviridaeVirus genome modificationDeletion of M51 gene and insertion of GFP geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell linePancreatic ductal adeonocarcinoma cell lineCell lineMIAPaCa-2Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for MIA PaCa2 cell lineIn-vivo virus concentration5.0E+7 pfuIn-vivo toxicityNA In-vivo resultReduction in tumor weight below 5 mg after 25 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectDownregulation of IFN-GammaClinical trialNAPMID22238308
IDOV_2409Virus nameVesicular stomatitis virusVirus strainVSV-Delta-M51-GFPVirus genome typeRNAVirus familyRhabdoviridaeVirus genome modificationDeletion of M51 gene and insertion of GFP geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell linePancreatic ductal adeonocarcinoma cell lineCell linePANC-1Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for MIA PANC-1 cell lineIn-vivo virus concentration5 × 10⁷ pfu In-vivo toxicityNA In-vivo resultReduction in tumor weight below 200 mg after 25 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectDownregulation of IFN-GammaClinical trialNAPMID22238308
IDOV_2410Virus nameVesicular stomatitis virusVirus strainVSV-Delta-M51-GFPVirus genome typeRNAVirus familyRhabdoviridaeVirus genome modificationDeletion of M51 gene and insertion of GFP geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell linePancreatic ductal adeonocarcinoma cell lineCell lineHPAF-IIConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for HPAF-II cell lineIn-vivo virus concentration5 × 10⁷ pfu In-vivo toxicityNA In-vivo resultReduction in tumor weight below 20 mg after 25 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectDownregulation of IFN-GammaClinical trialNAPMID22238308
IDOV_2411Virus nameVesicular stomatitis virusVirus strainVSV-Delta-M51-GFPVirus genome typeRNAVirus familyRhabdoviridaeVirus genome modificationDeletion of M51 gene and insertion of GFP geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell linePancreatic ductal adeonocarcinoma cell lineCell lineSU.86.86Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for U.86.86 cell lineIn-vivo virus concentration5 × 10⁷ pfu In-vivo toxicityNA In-vivo resultReduction in tumor weight below 20 mg after 25 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectDownregulation of IFN-GammaClinical trialNAPMID22238308
IDOV_2526Virus nameVaccinia virusVirus strainGLV-1h151Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationDeteltion of TK gene and addition of GFP geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman pancreatic cancer cell lineCell linePANC-1Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd:athymic nude mice xenografted for PANC-1 cell line(2.0E+6 cells)In-vivo virus concentration2.0E+6 pfuIn-vivo toxicityNA In-vivo resultDecrease in tumor volume below 2 after 34 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID22258815
IDOV_2527Virus nameVaccinia virusVirus strainGLV-1h151Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationDeteltion of TK gene and addition of GFP geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman pancreatic cancer cell lineCell linePANC-1Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd:athymic nude mice xenografted for PANC-1 cell line(2.0E+6 cells)In-vivo virus concentration2.0E+6 pfuIn-vivo toxicityNA In-vivo resultDecrease in tumor volume below 2 after 34 daysMode of deliveryIntravenousPathway inducedNAImmunogenic effectNAClinical trialNAPMID22258815
IDOV_2843Virus nameVaccinia virusVirus strainwild typeVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman colorectal cancer cell lineCell lineHCT-116Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd:athymic nude mice xenograft for HCT-116 (5.0E+6 cells)In-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultSignificant reduction in tumor volume after 42 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID23531320
IDOV_3002Virus namePoxvirusVirus strainCF33-hNISVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationInsertion of gene encoding human hNISVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman colorectal cancer cell lineCell lineHCT-116Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd:athymic nude mice xenograft for HCT-116 (2.0E+6 cells)In-vivo virus concentration1.0E+5 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor volume after 55 daysMode of deliveryIntratumoralPathway inducedImmunogenicity followed by virus induced cell deathImmunogenic effectNAClinical trialNAPMID31061881
IDOV_3003Virus namePoxvirusVirus strainCF33-hNISVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationInsertion of gene encoding human hNISVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman colorectal cancer cell lineCell lineHT-29Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd:athymic nude mice xenograft for HT-29 (5.0E+6 cells)In-vivo virus concentration1.0E+5 pfuIn-vivo toxicityNA In-vivo resultTumor volume reached 1500mm after day 50Mode of deliveryIntratumoralPathway inducedImmunogenicity followed by virus induced cell deathImmunogenic effectNAClinical trialNAPMID31061881
IDOV_3004Virus namePoxvirusVirus strainCF33-hNISVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationInsertion of gene encoding human hNISVirus aloneNoVirus in combination with drug/radiationVirus in combination with I-131Immune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman colorectal cancer cell lineCell lineHCT-116Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd:athymic nude mice xenograft for HCT-116 (2.0E+6 cells)In-vivo virus concentration1.0E+4 pfuIn-vivo toxicityNA In-vivo resultReduction in tumor volume below 100mm after 55 daysMode of deliveryIntravenousPathway inducedImmunogenicity followed by virus induced cell deathImmunogenic effectNAClinical trialNAPMID31061881
IDOV_3005Virus namePoxvirusVirus strainCF33-hNISVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationInsertion of gene encoding human hNISVirus aloneNoVirus in combination with drug/radiationVirus in combination with I-131Immune gene insertion in viral genomeNoSource of cell lineATCCOrigin of cell lineHuman colorectal cancer cell lineCell lineHT-29Concentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd:athymic nude mice xenograft for HT-29 (3.0E+9 cells)In-vivo virus concentration1.0E+4 pfuIn-vivo toxicityNA In-vivo resultReduction in tumor volume below 300mm after 45 daysMode of deliveryIntravenousPathway inducedImmunogenicity followed by virus induced cell deathImmunogenic effectNAClinical trialNAPMID31061881
IDOV_4108Virus nameVaccinia virusVirus strainVVstrain LIVP 6.1.1Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationMutant for J2R geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineUniversity of colorado, USAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd athymic nude mice xenograft for STSA-1 cell line (1.0E+6)In-vivo virus concentration1.0E+7 pfuIn-vivo toxicityNA In-vivo resultTumor volume reduced to 1000 mm compared to control 2500mm after 42 daysMode of deliveryIntravenousPathway inducedNAImmunogenic effectNAClinical trialNAPMID26205404
IDOV_4109Virus nameVaccinia virusVirus strainVVstrain GLV-5b451Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationDerived from LIVP6.1.1 by inserting glaf-2 gene into J2R locusVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineUniversity of colorado, USAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd athymic nude mice xenograft for STSA-1 cell line (1.0E+6)In-vivo virus concentration1.0E+7 pfuIn-vivo toxicityNA In-vivo resultTumor volume reduced to 200 mm compared to control 2500mm after 49 daysMode of deliveryIntravenousPathway inducedNAImmunogenic effectNAClinical trialNAPMID26205404
IDOV_4148Virus nameAdenovirusVirus strainAduPARE1AVirus genome typeDNAVirus familyAdenoviridaeVirus genome modificationAddition of E1A gene upstream of uPAR promoterVirus aloneNoVirus in combination with drug/radiationVirus in combination with gemcitabine (160mg/kg)Immune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for BxPC-3 (5.0E+5)In-vivo virus concentration5.0E+10 VP per cellIn-vivo toxicityNA In-vivo resultMedian survival time increased from 22 days to 57 days with combined tretamentMode of deliveryNAPathway inducedVirus induce apoptosis process leads to cancer cell deathImmunogenic effectNAClinical trialNAPMID26227809
IDOV_4149Virus nameAdenovirusVirus strainAduPARE1AVirus genome typeDNAVirus familyAdenoviridaeVirus genome modificationAddition of E1A gene upstream of uPAR promoterVirus aloneNoVirus in combination with drug/radiationVirus in combination with gemcitabine (160mg/kg)Immune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for PANC-1 (5.0E+5)In-vivo virus concentration5.0E+10 VP per cellIn-vivo toxicityNA In-vivo resultMedian survival time increased from 37 days to 79.5 days with combined tretamentMode of deliveryNAPathway inducedVirus induce apoptosis process leads to cancer cell deathImmunogenic effectNAClinical trialNAPMID26227809
IDOV_4190Virus nameMeasles virusVirus strainMV-lambda-NAPVirus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationGenetically engineered for expressing human lambda immunoglobulin chainVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic nude mice xenograft for MDA-231-lu-P4 (1.0E+6 cells)In-vivo virus concentration2.0E+6 TCID50In-vivo toxicityNA In-vivo resultAll mice dead after 100 daysMode of deliveryIntravenousPathway inducedVirus induce apoptosis process leads to cancer cell deathImmunogenic effectVirus and drug both cause induction of IL-24 expressionClinical trialIn clinical trialsPMID26272026
IDOV_4191Virus nameMeasles virusVirus strainMV-lambda-NAPVirus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationGenetically engineered for expressing human lambda immunoglobulin chainVirus aloneNoVirus in combination with drug/radiationVirus in combination with Alisertib 30mg/kg for 3 weeksImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic nude mice xenograft for MDA-231-lu-P4 (1.0E+6 cells)In-vivo virus concentration2.0E+6 TCID50In-vivo toxicityNA In-vivo resultMice median survival time increased to 82.5 days compared to controlMode of deliveryIntravenousPathway inducedVirus induce apoptosis process leads to cancer cell deathImmunogenic effectVirus and drug both cause induction of IL-24 expressionClinical trialIn clinical trialsPMID26272026
IDOV_4192Virus nameMeasles virusVirus strainMV-lambda-NAPVirus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationGenetically engineered for expressing human lambda immunoglobulin chainVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic nude mice xenograft for MDA-231-lu-P4 (2.0E+6), pleural effusion transthoracic cavityIn-vivo virus concentration5.0E+5 TCID50In-vivo toxicityNA In-vivo resultMice median survival increased to 57 daysMode of deliveryTransthoracicPathway inducedVirus induce apoptosis process leads to cancer cell deathImmunogenic effectVirus and drug both cause induction of IL-24 expressionClinical trialIn clinical trialsPMID26272026
IDOV_4193Virus nameMeasles virusVirus strainMV-lambda-NAPVirus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationGenetically engineered for expressing human lambda immunoglobulin chainVirus aloneYesVirus in combination with drug/radiationVirus in combination with Alisertib 30mg/kg for 3 weeksImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic nude mice xenograft for MDA-231-lu-P4 (2.0E+6), pleural effusion transthoracic cavityIn-vivo virus concentration5.0E+5 TCID50In-vivo toxicityNA In-vivo resultMice median survival increased to 74 days compared to control 57 daysMode of deliveryTransthoracicPathway inducedVirus induce apoptosis process leads to cancer cell deathImmunogenic effectVirus and drug both cause induction of IL-24 expressionClinical trialIn clinical trialsPMID26272026
IDOV_4438Virus nameVesicular stomatitis virusVirus strainRdBVirus genome typeRNAVirus familyRhabdoviridaeVirus genome modificationVirus expressing VSVG epitope, with no dletion in HI-loop, no addition of linkerVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismmale athymic nude mice xenograft for A549 (1.0E+7)In-vivo virus concentration5.0E+9 pfuIn-vivo toxicityNA In-vivo resultTumor volume become below 600 cubic millimeter after 71 days compared to control 1000Mode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID26430798
IDOV_4439Virus nameVesicular stomatitis virusVirus strainRdB-1L-VSVGVirus genome typeRNAVirus familyRhabdoviridaeVirus genome modificationVirus expressing VSVG epitope, with no dletion in HI-loop, addition of single linkerVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismmale athymic nude mice xenograft for A549 (1.0E+7)In-vivo virus concentration5.0E+9 pfuIn-vivo toxicityNA In-vivo resultTumor volume become below 100 cubic millimeter after 71 days compared to control 1000Mode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID26430798
IDOV_4440Virus nameVesicular stomatitis virusVirus strainRdBVirus genome typeRNAVirus familyRhabdoviridaeVirus genome modificationVirus expressing VSVG epitope, with no dletion in HI-loop, no addition of linkerVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismmale athymic nude mice xenograft for MCF7 (1.0E+7)In-vivo virus concentration5.0E+10 pfuIn-vivo toxicityNA In-vivo resultTumor volume become below 1500 cubic millimeter after 49 days compared to control 4000Mode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID26430798
IDOV_4441Virus nameVesicular stomatitis virusVirus strainRdB-1L-VSVGVirus genome typeRNAVirus familyRhabdoviridaeVirus genome modificationVirus expressing VSVG epitope, with no dletion in HI-loop, addition of single linkerVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismmale athymic nude mice xenograft for MCF7 (1.0E+7)In-vivo virus concentration5.0E+10 pfuIn-vivo toxicityNA In-vivo resultTumor volume become below 600 cubic millimeter after 49 days compared to control 4000Mode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID26430798
IDOV_4505Virus nameNewcastle disease virusVirus strainwild typeVirus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for HT1080 (5.0E+6)In-vivo virus concentration2.0E+7 pfuIn-vivo toxicityNA In-vivo resultTumor volume reduced to 300 cubic mm after 25 days compared to control 800 cubic mmMode of deliveryIntratumoralPathway inducedNAImmunogenic effectInduced expression of Type 1 IFN, NK cells and macrophagesClinical trialNAPMID27009956
IDOV_4506Virus nameNewcastle disease virusVirus strain73T-S-KmVirus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationInsertion of HNKMKS sequence in fusogenic site between 111 -116 nucleotideVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for HT1080 (5.0E+6)In-vivo virus concentration2.0E+7 pfuIn-vivo toxicityNA In-vivo resultTumor volume reduced to below 100 cubic mm after 25 days compared to control 800 cubic mmMode of deliveryIntratumoralPathway inducedNAImmunogenic effectInduced expression of Type 1 IFN, NK cells and macrophagesClinical trialNAPMID27009956
IDOV_4507Virus nameNewcastle disease virusVirus strain73T-R-198Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationInsertion of HNRTKR sequence in fusogenic site between 111 -116 nucleotideVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for HT1080 (5.0E+6)In-vivo virus concentration2.0E+7 pfuIn-vivo toxicityNA In-vivo resultTumor volume reduced to 300 cubic mm after 25 days compared to control 800 cubic mmMode of deliveryIntratumoralPathway inducedNAImmunogenic effectInduced expression of Type 1 IFN, NK cells and macrophagesClinical trialNAPMID27009956
IDOV_4508Virus nameNewcastle disease virusVirus strain73T-R-198Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationInsertion of HNRTKR sequence in fusogenic site between 111 -116 nucleotideVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for HT1080 (5.0E+6)In-vivo virus concentration1.0E+8 pfuIn-vivo toxicityNA In-vivo resultTumor volume reduced to below 500 cubic mm compared to control 1000 cubic mm after 25 daysMode of deliveryIntravenousPathway inducedNAImmunogenic effectInduced expression of Type 1 IFN, NK cells and macrophagesClinical trialNAPMID27009956
IDOV_4631Virus nameAdenovirusVirus strainAd5/3-delata 24Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationMutation in delta E3 and delta 24 geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic nude mice xenograft for UPCI SCC 090 (2.0E+6)In-vivo virus concentration3.5E+11 pfuIn-vivo toxicityNA In-vivo resultComplete ereduction in tumor volume after 30 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID27086483
IDOV_4632Virus nameAdenovirusVirus strainAd5/3-CB016Virus genome typeDNAVirus familyAdenoviridaeVirus genome modificationMutation in delta E3 geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismFemale athymic nude mice xenograft for UPCI SCC 090 (2.0E+6)In-vivo virus concentration3.5E+11 pfuIn-vivo toxicityNA In-vivo resultComplete ereduction in tumor volume after 30 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID27086483
IDOV_4698Virus nameHerpes simplex virusVirus strainRAMBOVirus genome typeDNAVirus familyHerpesviridaeVirus genome modificationAntiangiogenic Vstat120 expressing virusVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice subcutaneous xenograft for CAL27 (1.5E+7)In-vivo virus concentration2.0E+6 pfu on day 7 and 16In-vivo toxicityNA In-vivo resultMice treated with virus shows delayed tumor growth compared to control, one shows complete tumor regressionMode of deliveryIntratumoralPathway inducedNAImmunogenic effectInduce antitumor immune responseClinical trialNAPMID27119105
IDOV_4704Virus nameHerpes simplex virusVirus strainRAMBOVirus genome typeDNAVirus familyHerpesviridaeVirus genome modificationAntiangiogenic Vstat120 expressing virusVirus aloneNoVirus in combination with drug/radiationVirus combination with ATN-224 (0.7 mg/kg/day) an copper chelator showing synergistic effectImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for UM-SCC-74A (1.5E+7)In-vivo virus concentration2.0E+6 pfu on day 7In-vivo toxicityNA In-vivo resultIncreased in survival time and reduction in tumor volume to below 200 cubic mm comapred to control 700 cubic mmMode of deliveryIntratumoralPathway inducedNAImmunogenic effectInduce antitumor immune responseClinical trialNAPMID27119105
IDOV_4705Virus nameHerpes simplex virusVirus strainRAMBOVirus genome typeDNAVirus familyHerpesviridaeVirus genome modificationAntiangiogenic Vstat120 expressing virusVirus aloneNoVirus in combination with drug/radiationVirus combination with ATN-224 (0.7 mg/kg/day) an copper chelator showing synergistic effectImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice xenograft for CAL27 (1.5E+7)In-vivo virus concentration2.0E+6 pfu on day 7In-vivo toxicityNA In-vivo resultIncreased in survival time and reduction in tumor volume to below 500 cubic mm comapred to control 2000 cubic mmMode of deliveryIntratumoralPathway inducedNAImmunogenic effectInduce antitumor immune responseClinical trialNAPMID27119105
IDOV_5184Virus nameTanapoxvirusVirus strainwild typeVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice CrlNU-Foxn1 xenograft for cellosaurus cell line 5.0E+6 cellsIn-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultReduction in tumor growth 250 compared to 550 after 34 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID27738905
IDOV_5185Virus nameTanapoxvirusVirus strainTPV-delta15LVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationDeletion mutant for 15L geneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice CrlNU-Foxn1 xenograft for cellosaurus cell line 5.0E+6 cellsIn-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor volume compared to 550 after 34 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID27738905
IDOV_5186Virus nameTanapoxvirusVirus strainTPV-delta66RVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationDeletion mutant for tk 66ORFVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice CrlNU-Foxn1 xenograft for cellosaurus cell line 5.0E+6 cellsIn-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultReduction in tumor growth 150 compared to 550 after 34 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID27738905
IDOV_5187Virus nameTanapoxvirusVirus strainTPV-delta15Ldelta66RVirus genome typeDNAVirus familyPoxviridaeVirus genome modificationDeletion mutant for 15L gene and tk 66R locusVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic nude mice CrlNU-Foxn1 xenograft for cellosaurus cell line 5.0E+6 cellsIn-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultReduction in tumor growth 200 compared to 550 after 34 daysMode of deliveryIntratumoralPathway inducedNAImmunogenic effectNAClinical trialNAPMID27738905
IDOV_5638Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fibroblast HT1080 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regrression in tumor in 11 mice from complete 12 (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5639Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fibroblast HT1080 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regrression in tumor in 8 mice from complete 9 (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5640Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fibroblast HT1080 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regrression in tumor in all mice (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5641Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human ovarian carcinoma PA-1 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regrression in tumor in all mice (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5642Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human oral carcinoma KB (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete reduction in tumor in 7 mice from all 12 treated (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5643Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fmelanoma SKMEL (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete reduction in tumor in 5 mice from all 8 treated (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5644Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human lung carcinoma A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete reduction in tumor in 5 mice from all 8 treated (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5645Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human lung carcinoma A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regrression in tumor in all mice (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5646Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for humanglioblastoma U87MG (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete reduction in tumor in 1 mice from all 9 treated (tumor volume <10mm and >5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5647Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fibroblast HT1080 (10 million)In-vivo virus concentration1.0E+9 pfuIn-vivo toxicityNA In-vivo resultComplete regression in all tumor bearing mice (tumor volume <8.5 mm and > 5.5)Mode of deliveryIntravenouslyPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5648Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fibroblast HT1080 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in all tumor bearing mice (tumor volume <8.5 mm and > 5.5)Mode of deliveryIntravenouslyPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5649Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fibroblast HT1080 (10 million)In-vivo virus concentration6.0E+7 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor volume in 10 mice out of 11 (tumor volume <8.5 mm and > 5.5)Mode of deliveryIntravenouslyPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5650Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fibroblast HT1080 (10 million)In-vivo virus concentration2.0E+7 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor volume in 5 mice out of 11 (tumor volume <8.5 mm and > 5.5)Mode of deliveryIntravenouslyPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5651Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for human fibroblast HT1080 (10 million)In-vivo virus concentration2.0E+7 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor volume in 5 mice out of 7 (tumor volume <8.5 mm and > 5.5)Mode of deliveryIntravenouslyPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5652Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration1.5E+9 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 2 mice from total 8 tretated (tumor dimension 8 - 9.5mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5653Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration9.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 7 mice from total 8 tretated (tumor dimension 8 - 9.5mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5654Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 3 mice from total 8 tretated (tumor dimension 8 - 9.5mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5655Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration1.5E+9 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 2 mice from total 6 tretated (tumor volume <300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5656Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration9.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 3 mice from total 4 tretated (tumor dimension <300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5657Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 2 mice from total 6 tretated (tumor volume <300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5658Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 3 mice from total 5 tretated (tumor volume >300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5659Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in all mice(tumor volume >300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5660Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 4 mice from total 5 tretated (tumor volume>300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5661Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration1.5E+9 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in all mice (tumor dimension 10 - 11.5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5662Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 6 mice from 7 (tumor dimension 10 - 11.5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5663Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+7 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 5 mice from 7 (tumor dimension 10 - 11.5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5664Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+6 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in 5 mice from 7 (tumor dimension 10 - 11.5 mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5665Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration1.5E+9 pfuIn-vivo toxicityNA In-vivo resultComplete regression in tumor in all mice (tumor volume >300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5666Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+8 pfuIn-vivo toxicityNA In-vivo resultComplete reduction in tumor in 6 mice from 7 (tumor volume >300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5667Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+7 pfuIn-vivo toxicityNA In-vivo resultComplete reduction in tumor in 4 mice from 6 (tumor volume >300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5668Virus nameNewcastle disease virusVirus strainNDV-MK107Virus genome typeRNAVirus familyParamyxoviridaeVirus genome modificationNoneVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismAthymic mice xenograft for A375 (10 million)In-vivo virus concentration3.0E+6 pfuIn-vivo toxicityNA In-vivo resultComplete reduction in tumor in 4 mice from 6 (tumor volume >300mm)Mode of deliveryIntratumoralPathway inducedInduction of apoptosis by virus infectionImmunogenic effectInduction of IFN-Gamma productionClinical trialNAPMIDUS7470426
IDOV_5682Virus nameVaccinia virusVirus strainGLV-1h22Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationInsertion of Ruc-GFP, non coding DNA at F14.5L gene locus and TK and HA gene locus using psel vectorrespectivelyVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd athymic nude mice xenograft for GI-101A human breast carcinoma cells (5.0E+6)In-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultTumor volume become 261.8mm compared to control 240.8 mm after 33 daysMode of deliveryIntravenouslyPathway inducedInduction of apoptosisImmunogenic effectNAClinical trialNAPMIDUS8052968
IDOV_5683Virus nameVaccinia virusVirus strainGLV-1h68Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationInsertion of Ruc-GFP, non coding DNA at F14.5L gene locus and TK and HA gene locus using psel vectorrespectivelyVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd athymic nude mice xenograft for GI-101A human breast carcinoma cells (5.0E+6)In-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultTumor volume become 248.4mm compared to control 240.8 mm after 33 daysMode of deliveryIntravenouslyPathway inducedInduction of apoptosisImmunogenic effectNAClinical trialNAPMIDUS8052968
IDOV_5684Virus nameVaccinia virusVirus strainGLV-1h70Virus genome typeDNAVirus familyPoxviridaeVirus genome modificationInsertion of Ruc-GFP, LacZ gene locus and TK and HA gene locus using psel vectorrespectivelyVirus aloneYesVirus in combination with drug/radiationNoImmune gene insertion in viral genomeNoSource of cell lineNAOrigin of cell lineNACell lineNAConcentration of cell lineNAIn-vitro toxicityNAAssayNAIn-vitro virus concentrationNAIn-vitro resultNAModel organismHsd athymic nude mice xenograft for GI-101A human breast carcinoma cells (5.0E+6)In-vivo virus concentration5.0E+6 pfuIn-vivo toxicityNA In-vivo resultTumor volume become 216.8mm compared to control 240.8 mm after 33 daysMode of deliveryIntravenouslyPathway inducedInduction of apoptosisImmunogenic effectNAClinical trialNAPMIDUS8052968