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_192 | Virus nameHerpes simplex virus | Virus strainrQNestin34.5 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDeletion mutant for both copies of gamma 34.5 gene and ICP6 gene, re-addition of 34.5 gene under nestin promoter | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic nu/nu mice injected intracranially with GBM30 cells 1.0E+5 cells | In-vivo virus concentration5.0E+5 PFU (on 5 day) in total 8 mice | In-vivo toxicityNA | In-vivo result40% mice survived on 28th day | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26524593 |
IDOV_193 | Virus nameHerpes simplex virus | Virus strainrQNestin34.5 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDeletion mutant for both copies of gamma 34.5 gene and ICP6 gene, re-addition of 34.5 gene under nestin promoter | Virus aloneNo | Virus 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 genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic nu/nu mice injected intracranially with GBM30 cells 1.0E+5 cells | In-vivo virus concentration5.0E+5 PFU (on 5 day) in total 8 mice | In-vivo toxicityNA | In-vivo result80% mice survived on 28th day | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26524593 |
IDOV_357 | Virus nameAdenovirus | Virus strainAdhz60 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationE1b-deleted mutant | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model 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 AdLacZ | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26561948 |
IDOV_358 | Virus nameAdenovirus | Virus strainAdhz60 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationE1b-deleted mutant | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with temozolomide (TMZ) intraperitoneally at 50 mg/Kg for five consecutive days | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model 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 AdLacZ | Mode of deliveryIntratumorally | Pathway inducedJNK activation induces autophagy | Immunogenic effectNA | Clinical trialNA | PMID26561948 |
IDOV_359 | Virus nameAdenovirus | Virus strainAdLacZ | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationE1/E3-deleted mutant | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with temozolomide (TMZ) intraperitoneally at 50 mg/Kg for five consecutive days | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model 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 AdLacZ | Mode of deliveryIntratumorally | Pathway inducedJNK activation induces autophagy | Immunogenic effectNA | Clinical trialNA | PMID26561948 |
IDOV_376 | Virus nameHerpes simplex virus | Virus strainSeprehvir (HSV1716) | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationΔγ134.5 attenuated virus mutant | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model 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 survived | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26583803 |
IDOV_377 | Virus nameHerpes simplex virus | Virus strainSeprehvir (HSV1716) | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationΔγ134.5 attenuated virus mutant | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model 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 survived | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26583803 |
IDOV_378 | Virus nameHerpes simplex virus | Virus strainSeprehvir (HSV1716) | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationΔγ134.5 attenuated virus mutant | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model 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 survived | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26583803 |
IDOV_379 | Virus nameHerpes simplex virus | Virus strainSeprehvir (HSV1716) | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationΔγ134.5 attenuated virus mutant | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model 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 survived | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26583803 |
IDOV_392 | Virus nameVaccinia virus | Virus strainGLV-1h68 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHomozygous athymic female nude mice (subcutaneously injected with KMC-1 cells suspended in 50 μl Matrigel) | In-vivo virus concentration1.0E+7 PFU | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 30 cubic millimeter compared to control 200 cubic millimeter after 15 days | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26584530 |
IDOV_749 | Virus nameAdenovirus | Virus strainAdAFPp-E1A | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationThe viral mutant with E1A gene driven by AFP promoter | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHepG2 orthotopic liver xenograft tumor in Balb/c athymic nude | In-vivo virus concentrationNA | In-vivo toxicityNA | In-vivo resultReduction in tumor weight to 0.2 g compared to control 0.75 g after 18 days | Mode of deliveryintravenously | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27450327 |
IDOV_750 | Virus nameAdenovirus | Virus strainAdAFPp-E1A-122 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationThe viral insertion mutant with miR-122 target sequence into AdAFPp-E1A for negatively regulating E1A gene expression | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHepG2 orthotopic liver xenograft tumor in Balb/c athymic nude | In-vivo virus concentrationNA | In-vivo toxicityNA | In-vivo resultReduction in tumor weight to 0.2 g compared to control 0.75 g after 18 days | Mode of deliveryintravenously | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27450327 |
IDOV_751 | Virus nameAdenovirus | Virus strainAdTrack | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHepG2 orthotopic liver xenograft tumor in Balb/c athymic nude | In-vivo virus concentrationNA | In-vivo toxicityNA | In-vivo resultReduction in tumor weight to 0.85 g compared to control 0.75 g after 18 days | Mode of deliveryintravenously | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27450327 |
IDOV_752 | Virus nameAdenovirus | Virus strainAdAFPp-E1A-122 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationThe viral insertion mutant with miR-122 target sequence into AdAFPp-E1A for negatively regulating E1A gene expression | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHepG2 subcutaneous liver xenograft tumor in Balb/c athymic nude | In-vivo virus concentrationNA | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 0.8 cubic centimeter compared to control 2.4 cubic centimeter after 15 days | Mode of deliveryintravenously | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27450327 |
IDOV_838 | Virus nameHerpes simplex virus | Virus strainHSV-G207 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDeletion mutant of both copies of gamma 34.5 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic rat xenograft model for C85 cell line | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultNo response | Mode of deliveryDirect injection | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID10428757 |
IDOV_839 | Virus nameHerpes simplex virus | Virus strainHSV-G207 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDeletion mutant of both copies of gamma 34.5 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic rat xenograft model for C86 cell line | In-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 injection | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID10428757 |
IDOV_840 | Virus nameHerpes simplex virus | Virus strainHSV-G207 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDeletion mutant of both copies of gamma 34.5 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic rat xenograft model for HCT8 cell line | In-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 injection | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID10428757 |
IDOV_858 | Virus nameMeasles virus | Virus strainMV-Edm | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationRecombinant expressing a peptide | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomevirus expressing a marker peptide (MV-hCEA) | Source of cell lineNatural | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic mouse xenograft model for SKOV3 cell line | In-vivo virus concentration1.0E+7 pfu/ml | In-vivo toxicityNA | In-vivo resultMedian survival time increased by >105 days | Mode of deliverysubcutaneous | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID12183422 |
IDOV_859 | Virus nameMeasles virus | Virus strainMV-Edm | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationRecombinant expressing a peptide | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomevirus expressing a marker peptide (MV-hCEA) | Source of cell lineNatural | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic mouse xenograft model for SKOV3 cell line | In-vivo virus concentration10â·pfu/ml | In-vivo toxicityNA | In-vivo resultMedian survival time increased by >80 days | Mode of deliveryintraperitonial | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID12183422 |
IDOV_897 | Virus nameHerpes simplex virus | Virus strainMutant | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDeletion mutant for Gamma 34.5 | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd athymic nude mice xenograft for Hep 3B cancer cell line | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor nodes after 4 weeks | Mode of deliveryintraperitonial | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID12788648 |
IDOV_1103 | Virus nameAdenovirus | Virus strainZD55-IL-24 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAdenovirus expressing ZD55 gene and IL-24 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeExpressing IL-24 gene | Source of cell lineShanghai cell collection | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic BALB/c nude mice xenograft for SW620 cell line | In-vivo virus concentration5.0E+8 cells per well | In-vivo toxicityNA | In-vivo resultDecrease in tumor volume below 800mm³ as compared to control | Mode of deliveryIntratumoral injection | Pathway inducedApoptosis induction and cspase 3 activation | Immunogenic effectNA | Clinical trialNA | PMID15661558 |
IDOV_1104 | Virus nameAdenovirus | Virus strainAd-IL-24 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAdenovirus expressing IL-24 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeExpressing IL-24 gene | Source of cell lineShanghai cell collection | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic BALB/c nude mice xenograft for SW620 cell line | In-vivo virus concentration5.0E+8 cells per well | In-vivo toxicityNA | In-vivo resultDecrease in tumor volume below 600mm³ as compared to control | Mode of deliveryIntratumoral injection | Pathway inducedApoptosis induction and cspase 3 activation | Immunogenic effectNA | Clinical trialNA | PMID15661558 |
IDOV_1105 | Virus nameAdenovirus | Virus strainONYX-015 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineShanghai cell collection | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic BALB/c nude mice xenograft for SW620 cell line | In-vivo virus concentration5.0E+8 cells per well | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor volume | Mode of deliveryIntratumoral injection | Pathway inducedApoptosis induction and cspase 3 activation | Immunogenic effectNA | Clinical trialNA | PMID15661558 |
IDOV_1190 | Virus nameAdenovirus | Virus strainICOVIR-5 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationICOVIR-5 in combination with RAD001 drug (5mg/kg for 5 days) | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman glioblastoma cell line | Cell lineU-87 MG | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for U87MG cells | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction of tumor after 90 days in 20-40% of animals | Mode of deliveryNA | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID17557108 |
IDOV_1191 | Virus nameAdenovirus | Virus strainICOVIR-5 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationICOVIR-5 in combination with Temozolomide drug (7.5mg/kg for 5 days) | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman glioblastoma cell line | Cell lineU-87 MG | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for U87MG cells | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction of tumor after 90 days in 20-40% of animals | Mode of deliveryNA | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID17557108 |
IDOV_1665 | Virus nameHerpes simplex virus | Virus strainHSV-1 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeVirus expressing vstat120 gene | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice, injected with U87deltaEGFR cell line | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultSignificant increase in median survival time of mice | Mode of deliveryIntracranial | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID19844198 |
IDOV_1666 | Virus nameHerpes simplex virus | Virus strainHSV-1 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeVirus expressing vstat120 gene | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice, injected with GlideltaEGFR-H2B-RFP cell line | In-vivo virus concentration1.5E+6 cells | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume and increase in median survival time of mice | Mode of deliverySubcutaneously | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID19844198 |
IDOV_1915 | Virus nameVaccinia virus | Virus strainGLV-1h68 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineMalignan small cell canine carcinoma cell line | Cell lineMTH52c | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd athymic nude mice xenograft for MTH52c cell line | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultSignificant decrease in tumor volume after 42 days | Mode of deliveryNA | Pathway inducedNA | Immunogenic effectVirus cause increase expression of ApoA1, IL-2,11,18,IFN-gamma, IP-10, MCP-1,3,5,MIP-2,MMP-9 and TNF alpha | Clinical trialNA | PMID20631910 |
IDOV_2063 | Virus nameVaccinia virus | Virus strainGLV-1h68 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman hepatocellular carcinoma cell line | Cell linePLC | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic hsd nude mice xenograft for PLC cell line | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityReduction in tumor volume below 2000mm compared to control after 45 days | In-vivo resultNo response | Mode of deliveryNA | Pathway inducedInduction of apoptosis in cancer cell line | Immunogenic 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-2 | Clinical trialNA | PMID21779374 |
IDOV_2064 | Virus nameVaccinia virus | Virus strainGLV-1h68 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman hepatocellular carcinoma cell line | Cell lineHuh-7 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic hsd nude mice xenograft for PLC cell line | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityReduction in tumor volume below 3000mm compared to control after 35 days | In-vivo result | Mode of deliveryNA | Pathway inducedInduction of apoptosis in cancer cell line | Immunogenic 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-2 | Clinical trialNA | PMID21779374 |
IDOV_2408 | Virus nameVesicular stomatitis virus | Virus strainVSV-Delta-M51-GFP | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationDeletion of M51 gene and insertion of GFP gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell linePancreatic ductal adeonocarcinoma cell line | Cell lineMIAPaCa-2 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for MIA PaCa2 cell line | In-vivo virus concentration5.0E+7 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor weight below 5 mg after 25 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectDownregulation of IFN-Gamma | Clinical trialNA | PMID22238308 |
IDOV_2409 | Virus nameVesicular stomatitis virus | Virus strainVSV-Delta-M51-GFP | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationDeletion of M51 gene and insertion of GFP gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell linePancreatic ductal adeonocarcinoma cell line | Cell linePANC-1 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for MIA PANC-1 cell line | In-vivo virus concentration5 × 10ⷠpfu | In-vivo toxicityNA | In-vivo resultReduction in tumor weight below 200 mg after 25 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectDownregulation of IFN-Gamma | Clinical trialNA | PMID22238308 |
IDOV_2410 | Virus nameVesicular stomatitis virus | Virus strainVSV-Delta-M51-GFP | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationDeletion of M51 gene and insertion of GFP gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell linePancreatic ductal adeonocarcinoma cell line | Cell lineHPAF-II | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for HPAF-II cell line | In-vivo virus concentration5 × 10ⷠpfu | In-vivo toxicityNA | In-vivo resultReduction in tumor weight below 20 mg after 25 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectDownregulation of IFN-Gamma | Clinical trialNA | PMID22238308 |
IDOV_2411 | Virus nameVesicular stomatitis virus | Virus strainVSV-Delta-M51-GFP | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationDeletion of M51 gene and insertion of GFP gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell linePancreatic ductal adeonocarcinoma cell line | Cell lineSU.86.86 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for U.86.86 cell line | In-vivo virus concentration5 × 10ⷠpfu | In-vivo toxicityNA | In-vivo resultReduction in tumor weight below 20 mg after 25 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectDownregulation of IFN-Gamma | Clinical trialNA | PMID22238308 |
IDOV_2526 | Virus nameVaccinia virus | Virus strainGLV-1h151 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationDeteltion of TK gene and addition of GFP gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman pancreatic cancer cell line | Cell linePANC-1 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd:athymic nude mice xenografted for PANC-1 cell line(2.0E+6 cells) | In-vivo virus concentration2.0E+6 pfu | In-vivo toxicityNA | In-vivo resultDecrease in tumor volume below 2 after 34 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID22258815 |
IDOV_2527 | Virus nameVaccinia virus | Virus strainGLV-1h151 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationDeteltion of TK gene and addition of GFP gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman pancreatic cancer cell line | Cell linePANC-1 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd:athymic nude mice xenografted for PANC-1 cell line(2.0E+6 cells) | In-vivo virus concentration2.0E+6 pfu | In-vivo toxicityNA | In-vivo resultDecrease in tumor volume below 2 after 34 days | Mode of deliveryIntravenous | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID22258815 |
IDOV_2843 | Virus nameVaccinia virus | Virus strainwild type | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman colorectal cancer cell line | Cell lineHCT-116 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd:athymic nude mice xenograft for HCT-116 (5.0E+6 cells) | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume after 42 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID23531320 |
IDOV_3002 | Virus namePoxvirus | Virus strainCF33-hNIS | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationInsertion of gene encoding human hNIS | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman colorectal cancer cell line | Cell lineHCT-116 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd:athymic nude mice xenograft for HCT-116 (2.0E+6 cells) | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor volume after 55 days | Mode of deliveryIntratumoral | Pathway inducedImmunogenicity followed by virus induced cell death | Immunogenic effectNA | Clinical trialNA | PMID31061881 |
IDOV_3003 | Virus namePoxvirus | Virus strainCF33-hNIS | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationInsertion of gene encoding human hNIS | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman colorectal cancer cell line | Cell lineHT-29 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd:athymic nude mice xenograft for HT-29 (5.0E+6 cells) | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultTumor volume reached 1500mm after day 50 | Mode of deliveryIntratumoral | Pathway inducedImmunogenicity followed by virus induced cell death | Immunogenic effectNA | Clinical trialNA | PMID31061881 |
IDOV_3004 | Virus namePoxvirus | Virus strainCF33-hNIS | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationInsertion of gene encoding human hNIS | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with I-131 | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman colorectal cancer cell line | Cell lineHCT-116 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd:athymic nude mice xenograft for HCT-116 (2.0E+6 cells) | In-vivo virus concentration1.0E+4 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor volume below 100mm after 55 days | Mode of deliveryIntravenous | Pathway inducedImmunogenicity followed by virus induced cell death | Immunogenic effectNA | Clinical trialNA | PMID31061881 |
IDOV_3005 | Virus namePoxvirus | Virus strainCF33-hNIS | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationInsertion of gene encoding human hNIS | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with I-131 | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman colorectal cancer cell line | Cell lineHT-29 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd:athymic nude mice xenograft for HT-29 (3.0E+9 cells) | In-vivo virus concentration1.0E+4 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor volume below 300mm after 45 days | Mode of deliveryIntravenous | Pathway inducedImmunogenicity followed by virus induced cell death | Immunogenic effectNA | Clinical trialNA | PMID31061881 |
IDOV_4108 | Virus nameVaccinia virus | Virus strainVVstrain LIVP 6.1.1 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationMutant for J2R gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineUniversity of colorado, USA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd athymic nude mice xenograft for STSA-1 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume reduced to 1000 mm compared to control 2500mm after 42 days | Mode of deliveryIntravenous | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26205404 |
IDOV_4109 | Virus nameVaccinia virus | Virus strainVVstrain GLV-5b451 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationDerived from LIVP6.1.1 by inserting glaf-2 gene into J2R locus | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineUniversity of colorado, USA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd athymic nude mice xenograft for STSA-1 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume reduced to 200 mm compared to control 2500mm after 49 days | Mode of deliveryIntravenous | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26205404 |
IDOV_4148 | Virus nameAdenovirus | Virus strainAduPARE1A | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of E1A gene upstream of uPAR promoter | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with gemcitabine (160mg/kg) | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for BxPC-3 (5.0E+5) | In-vivo virus concentration5.0E+10 VP per cell | In-vivo toxicityNA | In-vivo resultMedian survival time increased from 22 days to 57 days with combined tretament | Mode of deliveryNA | Pathway inducedVirus induce apoptosis process leads to cancer cell death | Immunogenic effectNA | Clinical trialNA | PMID26227809 |
IDOV_4149 | Virus nameAdenovirus | Virus strainAduPARE1A | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of E1A gene upstream of uPAR promoter | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with gemcitabine (160mg/kg) | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for PANC-1 (5.0E+5) | In-vivo virus concentration5.0E+10 VP per cell | In-vivo toxicityNA | In-vivo resultMedian survival time increased from 37 days to 79.5 days with combined tretament | Mode of deliveryNA | Pathway inducedVirus induce apoptosis process leads to cancer cell death | Immunogenic effectNA | Clinical trialNA | PMID26227809 |
IDOV_4190 | Virus nameMeasles virus | Virus strainMV-lambda-NAP | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationGenetically engineered for expressing human lambda immunoglobulin chain | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic nude mice xenograft for MDA-231-lu-P4 (1.0E+6 cells) | In-vivo virus concentration2.0E+6 TCID50 | In-vivo toxicityNA | In-vivo resultAll mice dead after 100 days | Mode of deliveryIntravenous | Pathway inducedVirus induce apoptosis process leads to cancer cell death | Immunogenic effectVirus and drug both cause induction of IL-24 expression | Clinical trialIn clinical trials | PMID26272026 |
IDOV_4191 | Virus nameMeasles virus | Virus strainMV-lambda-NAP | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationGenetically engineered for expressing human lambda immunoglobulin chain | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with Alisertib 30mg/kg for 3 weeks | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic nude mice xenograft for MDA-231-lu-P4 (1.0E+6 cells) | In-vivo virus concentration2.0E+6 TCID50 | In-vivo toxicityNA | In-vivo resultMice median survival time increased to 82.5 days compared to control | Mode of deliveryIntravenous | Pathway inducedVirus induce apoptosis process leads to cancer cell death | Immunogenic effectVirus and drug both cause induction of IL-24 expression | Clinical trialIn clinical trials | PMID26272026 |
IDOV_4192 | Virus nameMeasles virus | Virus strainMV-lambda-NAP | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationGenetically engineered for expressing human lambda immunoglobulin chain | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic nude mice xenograft for MDA-231-lu-P4 (2.0E+6), pleural effusion transthoracic cavity | In-vivo virus concentration5.0E+5 TCID50 | In-vivo toxicityNA | In-vivo resultMice median survival increased to 57 days | Mode of deliveryTransthoracic | Pathway inducedVirus induce apoptosis process leads to cancer cell death | Immunogenic effectVirus and drug both cause induction of IL-24 expression | Clinical trialIn clinical trials | PMID26272026 |
IDOV_4193 | Virus nameMeasles virus | Virus strainMV-lambda-NAP | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationGenetically engineered for expressing human lambda immunoglobulin chain | Virus aloneYes | Virus in combination with drug/radiationVirus in combination with Alisertib 30mg/kg for 3 weeks | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic nude mice xenograft for MDA-231-lu-P4 (2.0E+6), pleural effusion transthoracic cavity | In-vivo virus concentration5.0E+5 TCID50 | In-vivo toxicityNA | In-vivo resultMice median survival increased to 74 days compared to control 57 days | Mode of deliveryTransthoracic | Pathway inducedVirus induce apoptosis process leads to cancer cell death | Immunogenic effectVirus and drug both cause induction of IL-24 expression | Clinical trialIn clinical trials | PMID26272026 |
IDOV_4438 | Virus nameVesicular stomatitis virus | Virus strainRdB | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationVirus expressing VSVG epitope, with no dletion in HI-loop, no addition of linker | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismmale athymic nude mice xenograft for A549 (1.0E+7) | In-vivo virus concentration5.0E+9 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become below 600 cubic millimeter after 71 days compared to control 1000 | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26430798 |
IDOV_4439 | Virus nameVesicular stomatitis virus | Virus strainRdB-1L-VSVG | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationVirus expressing VSVG epitope, with no dletion in HI-loop, addition of single linker | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismmale athymic nude mice xenograft for A549 (1.0E+7) | In-vivo virus concentration5.0E+9 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become below 100 cubic millimeter after 71 days compared to control 1000 | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26430798 |
IDOV_4440 | Virus nameVesicular stomatitis virus | Virus strainRdB | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationVirus expressing VSVG epitope, with no dletion in HI-loop, no addition of linker | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismmale athymic nude mice xenograft for MCF7 (1.0E+7) | In-vivo virus concentration5.0E+10 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become below 1500 cubic millimeter after 49 days compared to control 4000 | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26430798 |
IDOV_4441 | Virus nameVesicular stomatitis virus | Virus strainRdB-1L-VSVG | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationVirus expressing VSVG epitope, with no dletion in HI-loop, addition of single linker | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismmale athymic nude mice xenograft for MCF7 (1.0E+7) | In-vivo virus concentration5.0E+10 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become below 600 cubic millimeter after 49 days compared to control 4000 | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID26430798 |
IDOV_4505 | Virus nameNewcastle disease virus | Virus strainwild type | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for HT1080 (5.0E+6) | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume reduced to 300 cubic mm after 25 days compared to control 800 cubic mm | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectInduced expression of Type 1 IFN, NK cells and macrophages | Clinical trialNA | PMID27009956 |
IDOV_4506 | Virus nameNewcastle disease virus | Virus strain73T-S-Km | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationInsertion of HNKMKS sequence in fusogenic site between 111 -116 nucleotide | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for HT1080 (5.0E+6) | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume reduced to below 100 cubic mm after 25 days compared to control 800 cubic mm | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectInduced expression of Type 1 IFN, NK cells and macrophages | Clinical trialNA | PMID27009956 |
IDOV_4507 | Virus nameNewcastle disease virus | Virus strain73T-R-198 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationInsertion of HNRTKR sequence in fusogenic site between 111 -116 nucleotide | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for HT1080 (5.0E+6) | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume reduced to 300 cubic mm after 25 days compared to control 800 cubic mm | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectInduced expression of Type 1 IFN, NK cells and macrophages | Clinical trialNA | PMID27009956 |
IDOV_4508 | Virus nameNewcastle disease virus | Virus strain73T-R-198 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationInsertion of HNRTKR sequence in fusogenic site between 111 -116 nucleotide | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for HT1080 (5.0E+6) | In-vivo virus concentration1.0E+8 pfu | In-vivo toxicityNA | In-vivo resultTumor volume reduced to below 500 cubic mm compared to control 1000 cubic mm after 25 days | Mode of deliveryIntravenous | Pathway inducedNA | Immunogenic effectInduced expression of Type 1 IFN, NK cells and macrophages | Clinical trialNA | PMID27009956 |
IDOV_4631 | Virus nameAdenovirus | Virus strainAd5/3-delata 24 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationMutation in delta E3 and delta 24 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic nude mice xenograft for UPCI SCC 090 (2.0E+6) | In-vivo virus concentration3.5E+11 pfu | In-vivo toxicityNA | In-vivo resultComplete ereduction in tumor volume after 30 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27086483 |
IDOV_4632 | Virus nameAdenovirus | Virus strainAd5/3-CB016 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationMutation in delta E3 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismFemale athymic nude mice xenograft for UPCI SCC 090 (2.0E+6) | In-vivo virus concentration3.5E+11 pfu | In-vivo toxicityNA | In-vivo resultComplete ereduction in tumor volume after 30 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27086483 |
IDOV_4698 | Virus nameHerpes simplex virus | Virus strainRAMBO | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationAntiangiogenic Vstat120 expressing virus | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice subcutaneous xenograft for CAL27 (1.5E+7) | In-vivo virus concentration2.0E+6 pfu on day 7 and 16 | In-vivo toxicityNA | In-vivo resultMice treated with virus shows delayed tumor growth compared to control, one shows complete tumor regression | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectInduce antitumor immune response | Clinical trialNA | PMID27119105 |
IDOV_4704 | Virus nameHerpes simplex virus | Virus strainRAMBO | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationAntiangiogenic Vstat120 expressing virus | Virus aloneNo | Virus in combination with drug/radiationVirus combination with ATN-224 (0.7 mg/kg/day) an copper chelator showing synergistic effect | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for UM-SCC-74A (1.5E+7) | In-vivo virus concentration2.0E+6 pfu on day 7 | In-vivo toxicityNA | In-vivo resultIncreased in survival time and reduction in tumor volume to below 200 cubic mm comapred to control 700 cubic mm | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectInduce antitumor immune response | Clinical trialNA | PMID27119105 |
IDOV_4705 | Virus nameHerpes simplex virus | Virus strainRAMBO | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationAntiangiogenic Vstat120 expressing virus | Virus aloneNo | Virus in combination with drug/radiationVirus combination with ATN-224 (0.7 mg/kg/day) an copper chelator showing synergistic effect | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice xenograft for CAL27 (1.5E+7) | In-vivo virus concentration2.0E+6 pfu on day 7 | In-vivo toxicityNA | In-vivo resultIncreased in survival time and reduction in tumor volume to below 500 cubic mm comapred to control 2000 cubic mm | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectInduce antitumor immune response | Clinical trialNA | PMID27119105 |
IDOV_5184 | Virus nameTanapoxvirus | Virus strainwild type | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice CrlNU-Foxn1 xenograft for cellosaurus cell line 5.0E+6 cells | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor growth 250 compared to 550 after 34 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27738905 |
IDOV_5185 | Virus nameTanapoxvirus | Virus strainTPV-delta15L | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationDeletion mutant for 15L gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice CrlNU-Foxn1 xenograft for cellosaurus cell line 5.0E+6 cells | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor volume compared to 550 after 34 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27738905 |
IDOV_5186 | Virus nameTanapoxvirus | Virus strainTPV-delta66R | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationDeletion mutant for tk 66ORF | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice CrlNU-Foxn1 xenograft for cellosaurus cell line 5.0E+6 cells | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor growth 150 compared to 550 after 34 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27738905 |
IDOV_5187 | Virus nameTanapoxvirus | Virus strainTPV-delta15Ldelta66R | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationDeletion mutant for 15L gene and tk 66R locus | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic nude mice CrlNU-Foxn1 xenograft for cellosaurus cell line 5.0E+6 cells | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor growth 200 compared to 550 after 34 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27738905 |
IDOV_5638 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fibroblast HT1080 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regrression in tumor in 11 mice from complete 12 (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5639 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fibroblast HT1080 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regrression in tumor in 8 mice from complete 9 (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5640 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fibroblast HT1080 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regrression in tumor in all mice (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5641 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human ovarian carcinoma PA-1 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regrression in tumor in all mice (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5642 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human oral carcinoma KB (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor in 7 mice from all 12 treated (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5643 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fmelanoma SKMEL (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor in 5 mice from all 8 treated (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5644 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human lung carcinoma A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor in 5 mice from all 8 treated (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5645 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human lung carcinoma A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regrression in tumor in all mice (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5646 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for humanglioblastoma U87MG (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor in 1 mice from all 9 treated (tumor volume <10mm and >5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5647 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fibroblast HT1080 (10 million) | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in all tumor bearing mice (tumor volume <8.5 mm and > 5.5) | Mode of deliveryIntravenously | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5648 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fibroblast HT1080 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in all tumor bearing mice (tumor volume <8.5 mm and > 5.5) | Mode of deliveryIntravenously | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5649 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fibroblast HT1080 (10 million) | In-vivo virus concentration6.0E+7 pfu | In-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 deliveryIntravenously | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5650 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fibroblast HT1080 (10 million) | In-vivo virus concentration2.0E+7 pfu | In-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 deliveryIntravenously | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5651 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for human fibroblast HT1080 (10 million) | In-vivo virus concentration2.0E+7 pfu | In-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 deliveryIntravenously | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5652 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration1.5E+9 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 2 mice from total 8 tretated (tumor dimension 8 - 9.5mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5653 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration9.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 7 mice from total 8 tretated (tumor dimension 8 - 9.5mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5654 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 3 mice from total 8 tretated (tumor dimension 8 - 9.5mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5655 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration1.5E+9 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 2 mice from total 6 tretated (tumor volume <300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5656 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration9.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 3 mice from total 4 tretated (tumor dimension <300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5657 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 2 mice from total 6 tretated (tumor volume <300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5658 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 3 mice from total 5 tretated (tumor volume >300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5659 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in all mice(tumor volume >300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5660 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 4 mice from total 5 tretated (tumor volume>300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5661 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration1.5E+9 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in all mice (tumor dimension 10 - 11.5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5662 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 6 mice from 7 (tumor dimension 10 - 11.5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5663 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+7 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 5 mice from 7 (tumor dimension 10 - 11.5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5664 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+6 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in 5 mice from 7 (tumor dimension 10 - 11.5 mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5665 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration1.5E+9 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor in all mice (tumor volume >300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5666 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor in 6 mice from 7 (tumor volume >300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5667 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+7 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor in 4 mice from 6 (tumor volume >300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5668 | Virus nameNewcastle disease virus | Virus strainNDV-MK107 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismAthymic mice xenograft for A375 (10 million) | In-vivo virus concentration3.0E+6 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor in 4 mice from 6 (tumor volume >300mm) | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus infection | Immunogenic effectInduction of IFN-Gamma production | Clinical trialNA | PMIDUS7470426 |
IDOV_5682 | Virus nameVaccinia virus | Virus strainGLV-1h22 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationInsertion of Ruc-GFP, non coding DNA at F14.5L gene locus and TK and HA gene locus using psel vectorrespectively | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd athymic nude mice xenograft for GI-101A human breast carcinoma cells (5.0E+6) | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 261.8mm compared to control 240.8 mm after 33 days | Mode of deliveryIntravenously | Pathway inducedInduction of apoptosis | Immunogenic effectNA | Clinical trialNA | PMIDUS8052968 |
IDOV_5683 | Virus nameVaccinia virus | Virus strainGLV-1h68 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationInsertion of Ruc-GFP, non coding DNA at F14.5L gene locus and TK and HA gene locus using psel vectorrespectively | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd athymic nude mice xenograft for GI-101A human breast carcinoma cells (5.0E+6) | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 248.4mm compared to control 240.8 mm after 33 days | Mode of deliveryIntravenously | Pathway inducedInduction of apoptosis | Immunogenic effectNA | Clinical trialNA | PMIDUS8052968 |
IDOV_5684 | Virus nameVaccinia virus | Virus strainGLV-1h70 | Virus genome typeDNA | Virus familyPoxviridae | Virus genome modificationInsertion of Ruc-GFP, LacZ gene locus and TK and HA gene locus using psel vectorrespectively | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineNA | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismHsd athymic nude mice xenograft for GI-101A human breast carcinoma cells (5.0E+6) | In-vivo virus concentration5.0E+6 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 216.8mm compared to control 240.8 mm after 33 days | Mode of deliveryIntravenously | Pathway inducedInduction of apoptosis | Immunogenic effectNA | Clinical trialNA | PMIDUS8052968 |