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_37 | Virus nameAdenovirus | Virus strainoAd/DCN/LRP | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationInsertional mutant for DCN and LRP 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 organismBALB/c nude mice xenograft for MIA PaCa-2 cell line 5.0E+6 cells | In-vivo virus concentration2.0E+10 VP (on 0, 2, and 4 days) | In-vivo toxicitySlight hepatotoxicity | In-vivo resultReduction in tumor volume to 230 cubic millimeter compared to control 300 cubic millimeter after 46 days | Mode of deliveryIntravenously | Pathway inducedInhibits Wnt/β-catenin and TGF-β1 signaling pathways | Immunogenic effectIL-6 production increased by 3 folds as compared to normal | Clinical trialNA | PMID26471393 |
IDOV_38 | Virus nameAdenovirus | Virus strainoAd/DCN/LRP-PEG | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationInsertional mutant for DCN and LRP gene with polyethylene glycol | 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 organismBALB/c nude mice xenograft for MIA PaCa-2 cell line 5.0E+4 cells | In-vivo virus concentration2.0E+10 VP (on 0, 2, and 4 days) | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 198 cubic millimeter compared to control 300 cubic millimeter after 46 days | Mode of deliveryIntravenously | Pathway inducedInhibits Wnt/β-catenin and TGF-β1 signaling pathways | Immunogenic effectNA | Clinical trialNA | PMID26471393 |
IDOV_39 | Virus nameAdenovirus | Virus strainoAd/DCN/LRP-PEG-NT | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationInsertional mutant for DCN and LRP gene with NT-conjugated polyethylene glycol | 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 organismBALB/c nude mice xenograft for MIA PaCa-2 cell line 5.0E+4 cells | In-vivo virus concentration2.0E+10 VP (on 0, 2, and 4 days) | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 100 cubic millimeter compared to control 300 cubic millimeter after 46 days | Mode of deliveryIntravenously | Pathway inducedInhibits Wnt/β-catenin and TGF-β1 signaling pathways | Immunogenic effectNA | Clinical trialNA | PMID26471393 |
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_401 | Virus nameHerpes simplex virus | Virus strainICP10PK | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDeletion mutant with R1 domain poorly functional in HSV-1 | 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 organismXenograft male BALB/c nu/nu mice (subcutaneously injected with 1.0E+7 A3755 cells in 100 μl) | In-vivo virus concentration100 μl; 1.0E+6 PFU on day 7 | In-vivo toxicityNA | In-vivo resultOn day 29 , tumor growth ratio reached 2 as compared to 13 (tumour growth ratio - dividing each tumour volume measured over time by the initial tumour volume on day 7) | Mode of deliveryIntratumorally | Pathway inducedNA | Immunogenic effectMICA and TNF-alpha expressions are upregulated | Clinical trialNA | PMID26602205 |
IDOV_566 | Virus nameAdenovirus | Virus strainOBP-301 (telomelysin) | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationViral mutant with human telomerase reverse transcriptase (hTERT) promotor for selective replication in cancer cells | 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 BALB/c nu/nu mice inoculated subcutaneously with MNNG/HOS-Luc cells (5.0E+6 cells per site) | In-vivo virus concentration5.0E+7 PFU | In-vivo toxicityNA | In-vivo resultProliferating tumor cells expressing ki67 get reduced from 550 cells to 250 cells | Mode of deliveryDirect injection | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27356624 |
IDOV_567 | Virus nameAdenovirus | Virus strainOBP-301 (telomelysin) | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationViral mutant with human telomerase reverse transcriptase (hTERT) promotor for selective replication in cancer cells | Virus aloneNo | Virus in combination with drug/radiationViral strain in combination with cisplatin (CDDP, 4 mg/kg body weight ) and doxorubicin (DOX, 2 mg/kg body weight )[drugs were given intraperitoneally] | 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 BALB/c nu/nu mice inoculated subcutaneously with MNNG/HOS-Luc cells (5.0E+6 cells per site) | In-vivo virus concentration5.0E+7 PFU | In-vivo toxicityNA | In-vivo resultProliferating tumor cells expressing ki67 get reduced from 550 cells to 75 cells | Mode of deliveryDirect injection | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID27356624 |
IDOV_602 | Virus nameAlphavirus | Virus strainM1 | Virus genome typeRNA | Virus familyTogaviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationViral strain in combination with H89 (10 mg/kg/d), injected intraperitoneally | 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 BALB/c-nu/nu mice inoculated subcutaneously with HCT-116, 5.0E+6 cells per mouse | In-vivo virus concentration3.0E+7 PFU/d | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 0.2 cubic centimeter compared to control 1cubic centimeter after 27 days | Mode of deliveryintravenously | Pathway inducedActivates Caspase-3 | Immunogenic effectNA | Clinical trialNA | PMID27374176 |
IDOV_603 | Virus nameAlphavirus | Virus strainM1 | Virus genome typeRNA | Virus familyTogaviridae | 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 organismFemale BALB/c-nu/nu mice inoculated subcutaneously with HCT-116, 5.0E+6 cells per mouse | In-vivo virus concentration3.0E+7 PFU/d | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 0.76 cubic centimeter compared to control 1cubic centimeter after 27 days | Mode of deliveryintravenously | Pathway inducedActivates Caspase-3 (very small) | Immunogenic effectNA | Clinical trialNA | PMID27374176 |
IDOV_604 | Virus nameAlphavirus | Virus strainM1 | Virus genome typeRNA | Virus familyTogaviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationViral strain in combination with H89 (10 mg/kg/d), injected intraperitoneally | 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 BALB/c-nu/nu mice inoculated subcutaneously with Capan-1, 3.0E+6 cells per mouse | In-vivo virus concentration3.0E+7 PFU/d | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 0.1 cubic centimeter compared to control 1cubic centimeter after 23 days | Mode of deliveryintravenously | Pathway inducedActivates Caspase-3 | Immunogenic effectNA | Clinical trialNA | PMID27374176 |
IDOV_605 | Virus nameAlphavirus | Virus strainM1 | Virus genome typeRNA | Virus familyTogaviridae | 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 organismFemale BALB/c-nu/nu mice inoculated subcutaneously with Capan-1, 3.0E+6 cells per mouse | In-vivo virus concentration3.0E+7 PFU/d | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 0.2 cubic centimeter compared to control 1cubic centimeter after 23 days | Mode of deliveryintravenously | Pathway inducedActivates Caspase-3 (very small) | Immunogenic effectNA | Clinical trialNA | PMID27374176 |
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_829 | Virus nameAdenovirus | Virus strainSG611-VSTM1 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationA VSTM1 gene expression cassette containing VSTM1 cDNA, cytomegalovirus promoter and SV40 polyA was inserted into the genome of SG611 to generate SG611-VSTM1 | Virus aloneNo | Virus in combination with drug/radiationViral strain in combination with DNR 300 μg/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 organismXenograft BALB/c nu/nu female mice subcutaneously injected with 1.0E+7 × 10ⷠK562 cells in a total volume of 100 μl | In-vivo virus concentration1.0E+9 pfu/ml | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 20 cubic millimeter compared to control 880 cubic millimeter after 30 days | Mode of deliveryIntratumoral | Pathway inducedEnhanced apoptosis activation is observed | Immunogenic effectNA | Clinical trialNA | PMID27472927 |
IDOV_830 | Virus nameAdenovirus | Virus strainSG611-VSTM1 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationA VSTM1 gene expression cassette containing VSTM1 cDNA, cytomegalovirus promoter and SV40 polyA was inserted into the genome of SG611 to generate SG611-VSTM1 | 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 organismXenograft BALB/c nu/nu female mice subcutaneously injected with 1.0E+7 × 10ⷠK562 cells in a total volume of 100 μl | In-vivo virus concentration1.0E+9 pfu/ml | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 80 cubic millimeter compared to control 880 cubic millimeter after 30 days | Mode of deliveryIntratumoral | Pathway inducedEnhanced apoptosis activation is observed | Immunogenic effectNA | Clinical trialNA | PMID27472927 |
IDOV_831 | Virus nameAdenovirus | Virus strainSG611 | 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 organismXenograft BALB/c nu/nu female mice subcutaneously injected with 1.0E+7 × 10ⷠK562 cells in a total volume of 100 μl | In-vivo virus concentration1.0E+9 pfu/ml | In-vivo toxicityNA | In-vivo resultReduction in tumor volume to 120 cubic millimeter compared to control 880 cubic millimeter after 30 days | Mode of deliveryIntratumoral | Pathway inducedEnhanced apoptosis activation is observed | Immunogenic effectNA | Clinical trialNA | PMID27472927 |
IDOV_884 | Virus nameHerpes simplex virus | Virus strainJS1 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationJS1 strain mutant in ICP34.5 and ICP47 | 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 | AssayMTT assay | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for HT-29 cell | In-vivo virus concentration1.0E+8 pfu | In-vivo toxicityNA | In-vivo resultCompelte reduction of tumor after 28 days | Mode of deliveryintraperitonial | Pathway inducedNA | Immunogenic effectIncrease production of IFN-gamma | Clinical trialNA | PMID12595888 |
IDOV_916 | Virus nameHerpes simplex virus | Virus strainBaco-1 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationNon- fusogenic ligated with EGFP protein | 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 organismBALB/cByJIcrSmnHsd-scid mice orthotopic xenograft for prostate cancer cell line | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo result30% reduction in tumor volume | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15129429 |
IDOV_917 | Virus nameHerpes simplex virus | Virus strainSynco-2 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationFusogenic membrane ligated with GALV.fus protein | 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 organismBALB/cByJIcrSmnHsd-scid mice orthotopic xenograft for prostate cancer cell line | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo result50% reduction in tumor volume | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15129429 |
IDOV_918 | Virus nameHerpes simplex virus | Virus strainSynco-2D | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDouble fusogenic expressing EGFP and GALV.fus protein | 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 organismBALB/cByJIcrSmnHsd-scid mice orthotopic xenograft for prostate cancer cell line | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo result60% reduction in tumor volume | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15129429 |
IDOV_919 | Virus nameHerpes simplex virus | Virus strainBaco-1 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationNon- fusogenic ligated with EGFP protein | 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 organismBALB/cByJIcrSmnHsd-scid mice metastatic lung metastatic model | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultLung metastasis were not detected after 40 days when stained with bouins fixative | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15129429 |
IDOV_920 | Virus nameHerpes simplex virus | Virus strainSynco-2 | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationFusogenic membrane ligated with GALV.fus protein | 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 organismBALB/cByJIcrSmnHsd-scid mice metastatic lung metastatic model | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultLung metastasis were not detected after 40 days when stained with bouins fixative | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15129429 |
IDOV_921 | Virus nameHerpes simplex virus | Virus strainSynco-2D | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationDouble fusogenic expressing EGFP and GALV.fus protein | 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 organismBALB/cByJIcrSmnHsd-scid mice metastatic lung metastatic model | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultLung metastasis were not detected after 40 days when stained with bouins fixative | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15129429 |
IDOV_922 | Virus nameAdenovirus | Virus strainCNHK-300 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of 3 hTERT promoter in E boxes of genome | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineSynthesized | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultTumor volume decreases to 600 mm3 after 20 days as compared to control | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15243805 |
IDOV_923 | 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 lineOnyx pharmaceutical | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultTumor volume decreases to 200 mm3 after 20 days as compared to control | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15243805 |
IDOV_924 | Virus nameAdenovirus | Virus strainCNHK-300 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of 3 hTERT promoter in E boxes of genome | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineSynthesized | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultTumor volume decreases to 200 mm3 after 20 days as compared to control | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15243805 |
IDOV_925 | Virus nameAdenovirus | Virus strainCNHK-300 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of 3 hTERT promoter in E boxes of genome | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineSynthesized | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice | In-vivo virus concentration5.0E+8 pfu | In-vivo toxicityNA | In-vivo resultTumor volume decreases to 500 mm3 after 20 days as compared to control | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15243805 |
IDOV_926 | Virus nameAdenovirus | Virus strainCNHK-300 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of 3 hTERT promoter in E boxes of genome | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineSynthesized | Origin of cell lineNA | Cell lineNA | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultTumor volume decreases to 400 mm3 after 20 days as compared to control | Mode of deliveryTail vein injection of virus | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID15243805 |
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_1136 | Virus nameSindbis virus | Virus strainAR339 | Virus genome typeRNA | Virus familyTogaviridae | 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 organismBALB/c nude mice xenograft for HeLaS3 cell line | In-vivo virus concentration1.0E+6 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor volume after 30 days | Mode of deliveryIntratumoral injection | Pathway inducedApoptosis induction in cancer cell lines | Immunogenic effectNA | Clinical trial | PMID15958641 |
IDOV_1137 | Virus nameSindbis virus | Virus strainAR339 | Virus genome typeRNA | Virus familyTogaviridae | 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 organismBALB/c nude mice xenograft for C33A cell line | In-vivo virus concentration1.0E+6 pfu | In-vivo toxicityNA | In-vivo resultComplete reduction in tumor volume after 30 days | Mode of deliveryIntratumoral injection | Pathway inducedApoptosis induction in cancer cell lines | Immunogenic effectNA | Clinical trial | PMID15958641 |
IDOV_1138 | Virus nameSindbis virus | Virus strainAR339 | Virus genome typeRNA | Virus familyTogaviridae | 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 organismBALB/c nude mice xenograft for C33A cell line | In-vivo virus concentration1.0E+6 pfu | In-vivo toxicityNA | In-vivo resultRediction in tumor volume to 200mm after 50 days | Mode of deliveryIntravenous injection | Pathway inducedApoptosis induction in cancer cell lines | Immunogenic effectNA | Clinical trial | PMID15958641 |
IDOV_1146 | Virus nameHerpes simplex virus | Virus strainMutant | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationMutant for gamma 34.5, lacZ and alpha 47 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 organismBALB/c nude mice xenograft for Human prostatic cancer HONDA | In-vivo virus concentration2.0E+6 pfu | In-vivo toxicityNA | In-vivo resultTotal reduction in tumor volume in 2 mice after 3 days | Mode of deliveryIntraneoplastically | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID16278413 |
IDOV_1148 | Virus nameHerpes simplex virus | Virus strainMutant | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationMutant for gamma 34.5, lacZ and alpha 47 gene | Virus aloneNo | Virus in combination with drug/radiationVirus strain in combination with flutamide | 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 organismBALB/c nude mice xenograft for Human prostatic cancer HONDA | In-vivo virus concentrationNo | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume as compared to flutamide alone | Mode of deliverySubcutaneous | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID16278413 |
IDOV_1314 | Virus nameAdenovirus | Virus strainOBP-301 | 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 organismBALB/c nude mice xenograft for Human prostate cancer cell line LNCaP | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor size after day 20, 3 times administration | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID18274558 |
IDOV_1351 | Virus nameAdenovirus | Virus strainAdCN101 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modification24bp deletion between E1Ap and E1A | 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 organismBALB/c nude mice, xenograft for BEL7404 | In-vivo virus concentration2.0E+8 pfu | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume after 7 weeks and increase in survival | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID18281783 |
IDOV_1352 | Virus nameAdenovirus | Virus strainAdCN102 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of hTERT promoter ahead of E1A | 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 organismBALB/c nude mice, xenograft for BEL7404 | In-vivo virus concentration2.0E+8 pfu | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume after 7 weeks and increase in survival | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID18281783 |
IDOV_1353 | Virus nameAdenovirus | Virus strainAdCN103 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modification24 bp deletion in hTERT 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 organismBALB/c nude mice, xenograft for BEL7404 | In-vivo virus concentration2.0E+8 pfu | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume after 7 weeks and increase in survival | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID18281783 |
IDOV_1384 | Virus nameAdenovirus | Virus strainZD55-Ki67 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationExpressing Ki67 ShRNA | 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 organismBALB/c nude mice xenograft for Human prostate cancer cell line LNCaP | In-vivo virus concentration7.0E+8 cells per well | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor size after 9 weeks | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis | Immunogenic effectNA | Clinical trialNA | PMID18690204 |
IDOV_1442 | Virus nameAdenovirus | Virus strainZD-55-IL-18 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeVirus expressing IL-18 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 organismBALB/c mice xenograft for A375 | In-vivo virus concentration7.0E+8 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor volume after 7 weeks | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis, activation of caspase 3 | Immunogenic effectNA | Clinical trialNA | PMID19498459 |
IDOV_1727 | Virus nameMeasles virus | Virus strainMV-Edm strain | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationMV-NPL virus , addition of P, N and L 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 organismBALB/c nude mice xenograft for A-498 cells | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultSurvival rate increased in 55% of animals | Mode of deliveryIntratumoral | Pathway inducedVirus induce apoptosis in cancer cells | Immunogenic effectInduce expression of IFN-gamma, an antiviral protein | Clinical trialNA | PMID20051938 |
IDOV_1728 | Virus nameMeasles virus | Virus strainMV-Edm strain | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationMV-P virus , addition of P 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 organismBALB/c nude mice xenograft for A-498 cells | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultSurvival rate increased in 11% of animals | Mode of deliveryIntratumoral | Pathway inducedVirus induce apoptosis in cancer cells | Immunogenic effectInduce expression of IFN-gamma, an antiviral protein | Clinical trialNA | PMID20051938 |
IDOV_1729 | Virus nameMeasles virus | Virus strainMV-Edm strain | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationMV-Etag 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 organismBALB/c nude mice xenograft for A-498 cells | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultNo effect on increase in survival time | Mode of deliveryIntratumoral | Pathway inducedVirus induce apoptosis in cancer cells | Immunogenic effectInduce expression of IFN-gamma, an antiviral protein | Clinical trialNA | PMID20051938 |
IDOV_2093 | Virus nameAdenovirus | Virus strainMutant | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationDeletion of E1BK55KD gene and addition of shMPP1 expressing cassette | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeVirus expressing IL-24 gene | Source of cell lineNA | Origin of cell lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for SW620 cell line (5.0E+6 cells) | In-vivo virus concentration2.0E+9 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor volume below 100 mm after 9 weeks | Mode of deliveryNA | Pathway inducedInduction of apoptosis | Immunogenic effectNA | Clinical trialNA | PMID21794078 |
IDOV_2138 | Virus nameAdenovirus | Virus strainMutant | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationDeletion of E1BK55KD gene and addition of TRAIL gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeVirus expressing TRAIL gene | 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 organismBALB/c mice xenograft for Huh7 cell line (5.0E+6 × 10ⶠpfu) | In-vivo virus concentration2.0E+9 pfu | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume below 100mm and increase in median survival time after 57 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis in cancer as measured by TUNEL assay | Immunogenic effectNA | Clinical trialNA | PMID21979578 |
IDOV_2209 | Virus nameHerpes simplex virus | Virus strainHSV-1-G47-delta | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationMutant for Gamma34.5, ICP6 and alpha47 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineHongkong university | Origin of cell lineHuman nasopharyngeal carcinoma cell line | Cell lineCNE-2 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for CNE-2 cell line (1.0E+6 × 10ⶠcells) | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultVirus treated mice shows complete regression in tumor and exhibit longer survival time | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID22059912 |
IDOV_2210 | Virus nameHerpes simplex virus | Virus strainHSV-1-G47-delta | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationMutant for Gamma34.5, ICP6 and alpha47 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineHongkong university | Origin of cell lineHuman nasopharyngeal carcinoma cell line | Cell lineSUNE-1 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SUNE-1 cell line (5.0E+5 × 10ⵠcells) | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultVirus treated mice shows complete regression in tumor and exhibit longer survival time | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID22059912 |
IDOV_2211 | Virus nameNewcastle disease virus | Virus strainwild type | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with cisplatin | Immune gene insertion in viral genomeNo | Source of cell lineChinese academy of sciece | Origin of cell lineHuman small cell lung cancer cell line | Cell lineA549 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for A549 cell line | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume decreased to 500mm after 57 days | Mode of deliveryIntratumoral | Pathway inducedInduction of caspase and apoptotic pathway as detected by Hoechst staining and TUNEL assay | Immunogenic effectNA | Clinical trialNA | PMID22095029 |
IDOV_2252 | Virus nameHerpes simplex virus | Virus strainHSV-1-G47-delta | Virus genome typeDNA | Virus familyHerpesviridae | Virus genome modificationMutant for Gamma34.5, ICP6 and alpha47 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineState key laboratory of oncology China | Origin of cell lineHuman breast cancer cell line | Cell lineMDA-MB-435 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for MDA-MB-435(1.0E+6 × 10â¶) | In-vivo virus concentration2.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume decreased by 9 fold after 56 days | Mode of deliveryIntratumoral | Pathway inducedCaspase activation | Immunogenic effectNA | Clinical trialNA | PMID22108767 |
IDOV_2553 | Virus nameAdenovirus | Virus strainAD55-Apoptin | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationDeletion of E1B gene and insertion of Apoptin gene | 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 organismBALB/c nude mice xenograft for Huh7 cell line (1.0E+7) | In-vivo virus concentration3.0E+8 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor volume below 425mm after 16 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apotosis as measured by TUNEL assay | Immunogenic effectNA | Clinical trialNA | PMID22321574 |
IDOV_2578 | Virus nameAdenovirus | Virus strainSG600-IL-24+IFN | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationDeletion of E1B gene and insertion of IL-24 gene and addition of IN | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeVirus expressing IL-24 gene and IFN gene | Source of cell lineATCC | Origin of cell lineHuman hepatocellular carcinoma cell line | Cell lineHCCLM3 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for HCCLM3 cell line | In-vivo virus concentration2.0E+8 pfu | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume from the onset of tretament and till the end of 42 days and increase in median survival time | Mode of deliveryIntratumoral | Pathway inducedCombined therapy increases STAT1, SOCS1 and apoptosis | Immunogenic effectCombined therapy decreases expression of MMP-2, XIAP,OPN and VEGF | Clinical trialNA | PMID22569271 |
IDOV_2605 | Virus nameAdenovirus | Virus strainAd.enAFP-E1A-delta-E1B-IL-24 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationDeletion of E1A, E1B and addition of AFP and IL-24 | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeVirus expressing IL-24 gene | Source of cell lineATCC | Origin of cell lineHuman liver cancer cell line | Cell lineHuh-7 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for Huh7 cell line (5.0E+6 cells) | In-vivo virus concentration4.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor after 28 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis in cancer | Immunogenic effectUpregulation of GADD34 | Clinical trialNA | PMID22790965 |
IDOV_2630 | Virus nameAdenovirus | Virus strainAd-hTERT-E1a-Apoptin | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of E1a and apoptin before hTERT promoter | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineType culture collection of chines academy, shanghai | Origin of cell lineHuman gastric cancer cell line | Cell lineSGC-7901 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for SGC7901 (1.0E+6 cells) | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor after 9 weeks and increase in median survival time upto 55 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis in cancer | Immunogenic effectNA | Clinical trialNA | PMID22842823 |
IDOV_2631 | Virus nameAdenovirus | Virus strainAd-hTERT-E1a-Apoptin | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of E1a and apoptin before hTERT promoter | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineType culture collection of chines academy, shanghai | Origin of cell lineHuman gastric cancer cell line | Cell lineSGC-7901 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for SGC7901 (1.0E+6 cells) | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume and increase in median survival time ipto 345 days | Mode of deliveryIntravenous | Pathway inducedInduction of apoptosis in cancer | Immunogenic effectNA | Clinical trialNA | PMID22842823 |
IDOV_2664 | Virus nameAdenovirus | Virus strainSG500-dNK | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of deoxyribonucleoside kinase | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with drug dFdC (1 micromolar) | Immune gene insertion in viral genomeNo | Source of cell lineShanghai cell collection | Origin of cell lineHuman breast cancer cell line | Cell lineMDA-MB-231 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for MDA-MB-231(5.0E+6 cells) | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultIncrease in median survival time to more than 100 days compared to control and reduction in tumor volume 663.85 +/- 379.39mm compared to control 1336.46 +/- 614.81 | Mode of deliveryNA | Pathway inducedCombination of drug and virus increase the apoptosis process | Immunogenic effectNA | Clinical trialNA | PMID23000515 |
IDOV_2755 | Virus nameAdenovirus | Virus strainAdCN205 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationVirus strain in combination with miR-34-a | Immune gene insertion in viral genomeVirus expressing IL-24 gene | 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 organismBALB/c nude mice xenograft for Huh cell (2.0E+6 cell) | In-vivo virus concentration7.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor volume after 49 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis, G1 arrest and sensescence | Immunogenic effectInhibition of oncogene and antiapototic gene | Clinical trialNA | PMID23292172 |
IDOV_2805 | Virus nameAdenovirus | Virus strainAd.sp-E1A-TSLC1 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationDeletion of 24bp with in E1A gene and insertion of TSLC1 gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman lung cancer cell line | Cell lineA549 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for A549 | In-vivo virus concentration5.0E+8 pfu | In-vivo toxicityNA | In-vivo resultSignificant reduction in tumor volume and increased in survival rate fro 15% to 87% at day 60 | Mode of deliveryIntratumoral | Pathway inducedInduction of apotosis by virus in cancer cell line as measured by TUNEL assay | Immunogenic effectNA | Clinical trialNA | PMID23503473 |
IDOV_2812 | Virus nameAdenovirus | Virus strainG47-delta | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationVirus strain in combination with palcitaxel (16 nm) | Immune gene insertion in viral genomeNo | Source of cell lineSun-sen university cancer centre, china | Origin of cell lineHuman breast cancer cell line | Cell lineMDA-MB-468 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for MDA-MB-468 (5.0E+6 cells) | In-vivo virus concentration2.0E+5 pfu | In-vivo toxicityNA | In-vivo resultReduction in tumor volume after 35 days | Mode of deliveryIntratumoral | Pathway inducedMitotic arrest and induction of apoptosis | Immunogenic effectNA | Clinical trialNA | PMID23525624 |
IDOV_2866 | Virus nameAdenovirus | Virus strainSG7605-11R-p53 | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationAddition of p53 gene and 11R CPP | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineEastern hepatobility hospital | Origin of cell lineGallbladder cancer cell line | Cell lineEH-GB2 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for EH-GB2 | In-vivo virus concentration1.0E+9 pfu | In-vivo toxicityNA | In-vivo resultSignficant reduction in tumor volume after day 30 and increase in median survival time | Mode of deliveryIntratumoral | Pathway inducedIncrease in apoptosis rate to 67% in cancer cell compared to normal | Immunogenic effectNA | Clinical trialNA | PMID23727990 |
IDOV_2931 | Virus nameMeasles 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 lineLaboratory grown own culture | Origin of cell lineLeukemia cell line | Cell lineU937 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for U937 | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed to below 12.5 mm after 14 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus alone and in combination | Immunogenic effectNA | Clinical trialNA | PMID25193462 |
IDOV_2932 | Virus nameMumps 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 lineLaboratory grown own culture | Origin of cell lineLeukemia cell line | Cell lineU937 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for U937 | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed to below 5 mm after 14 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus alone and in combination | Immunogenic effectNA | Clinical trialNA | PMID25193462 |
IDOV_2933 | Virus nameMeasles and mumps virus | Virus strainwild type | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationMeasles in combination with mumps | Immune gene insertion in viral genomeNo | Source of cell lineLaboratory grown own culture | Origin of cell lineLeukemia cell line | Cell lineU937 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for U937 | In-vivo virus concentration1.0E+5 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed near to 2.5 mm after 14 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus alone and in combination | Immunogenic effectNA | Clinical trialNA | PMID25193462 |
IDOV_2934 | Virus nameNewcastle disease virus | Virus strainwild type | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationExpressing rl gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell linePeking university china | Origin of cell lineHuman lung cancer cell line | Cell lineA549 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for A549 cell line (6.3E+8) | In-vivo virus concentration6.3E+8 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed to 274 +/- 114.20 compared to control 271.78 +/- 110.79 after day 1 | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus | Immunogenic effectNA | Clinical trialNA | PMID25364430 |
IDOV_2935 | Virus nameNewcastle disease virus | Virus strainwild type | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationExpressing rl gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell linePeking university china | Origin of cell lineHuman lung cancer cell line | Cell lineA549 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for A549 cell line (6.3E+8) | In-vivo virus concentration6.3E+8 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed to 444.18 +/- 111.22 compared to control 591.45 +/- 244.50 after day 7 | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus | Immunogenic effectNA | Clinical trialNA | PMID25364430 |
IDOV_2936 | Virus nameNewcastle disease virus | Virus strainwild type | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationExpressing rl gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell linePeking university china | Origin of cell lineHuman lung cancer cell line | Cell lineA549 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for A549 cell line (6.3E+8) | In-vivo virus concentration6.3E+8 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed to 657.56 +/- 176.74 compared to control 1483.21 +/- 446.75 after 14 day | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus | Immunogenic effectNA | Clinical trialNA | PMID25364430 |
IDOV_2937 | Virus nameNewcastle disease virus | Virus strainwild type | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationExpressing rl gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell linePeking university china | Origin of cell lineHuman lung cancer cell line | Cell lineA549 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for A549 cell line (6.3E+8) | In-vivo virus concentration6.3E+8 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed to 804.96 +/- 176.74 compared to control 1127.88 +/- 274.09 after 21 days | Mode of deliveryIntratumoral | Pathway inducedInduction of apoptosis by virus | Immunogenic effectNA | Clinical trialNA | PMID25364430 |
IDOV_3137 | Virus nameSendai virus | Virus strainuPA2 | Virus genome typeRNA | Virus familyParamyxoviridae | Virus genome modificationDeletion of M, F gen at cytoplasmic location | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineJapan collection of research bioresources cell bank | Origin of cell lineHuman anaplastic thyroid carcinoma cell line | Cell lineKHM-5M | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBALB/c nude mice xenograft for KHM-5M cell line (2.5E+5) | In-vivo virus concentration1.0E+6 CIU per dose | In-vivo toxicityNA | In-vivo resultReduction in tumor weight and increase in survival time 41.6 +/- 15 days | Mode of deliveryIntratumoral | Pathway inducedCaspase dependent induction of apoptosis in vivo and in vitro | Immunogenic effectNA | Clinical trialNA | PMID30969451 |
IDOV_3175 | Virus nameSemliki forest virus | Virus strainSFV-VA7 | Virus genome typeRNA | Virus familyTogaviridae | 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 prostate cancer cell line | Cell lineLNCaP | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismCAnM.Cg-Foxn1nu/Crl Balb/c nude mice subcutaneous xenograft for LNCaP (5.0E+6) | In-vivo virus concentration1.0E+6 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor volume after 20 days | Mode of deliveryIntraperitoneal | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID28557974 |
IDOV_3176 | Virus nameSemliki forest virus | Virus strainSFV-VA7 | Virus genome typeRNA | Virus familyTogaviridae | 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 prostate cancer cell line | Cell lineLNCaP | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismCAnM.Cg-Foxn1nu/Crl Balb/c nude mice subcutaneous xenograft for LNCaP (5.0E+6) | In-vivo virus concentration1.0E+6 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor volume after 20 days | Mode of deliveryIntraperitoneal | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID28557974 |
IDOV_3297 | Virus nameMaraba virus | Virus strainMG1 | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationNone | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineMurine sarcoma cell line | Cell lineS180 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice isograft for S180 mouse tumor cell line (1.0E+6) | In-vivo virus concentration1.0E+8 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor volume after 97 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectGenration of memory immune response by incresing production of cytokines | Clinical trialNA | PMID28568891 |
IDOV_3298 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 81.1% as compared to control 100% after day 3 | Mode of deliveryIntratumoral | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3299 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 89.7% as compared to control 100% after day 5 | Mode of deliveryIntratumoral | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3300 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 80.7% as compared to control 100% after day 8 | Mode of deliveryIntratumoral | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3301 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 71.9% as compared to control 100% after day 10 | Mode of deliveryIntratumoral | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3302 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 68.1% as compared to control 100% after day 12 | Mode of deliveryIntratumoral | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3303 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 58.4% as compared to control 100% after day 15 | Mode of deliveryIntratumoral | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3304 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 57.1% as compared to control 100% after day 17 | Mode of deliveryIntratumoral | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3305 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 58.3% as compared to control 100% after day 19 | Mode of deliveryIntratumoral | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3306 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 67.8% as compared to control 100% after day 3 | Mode of deliveryIntravenous | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3307 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 60.8% as compared to control 100% after day 5 | Mode of deliveryIntravenous | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3308 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 62.4% as compared to control 100% after day 8 | Mode of deliveryIntravenous | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3309 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 64.7% as compared to control 100% after day 10 | Mode of deliveryIntravenous | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3310 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 64.4% as compared to control 100% after day 12 | Mode of deliveryIntravenous | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3311 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 61.5% as compared to control 100% after day 15 | Mode of deliveryIntravenous | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3312 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 59.7% as compared to control 100% after day 17 | Mode of deliveryIntravenous | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3313 | Virus nameNewcastle disease virus | Virus strainR2B mukteshwar strain | 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 lineHuman colon cancer cell line | Cell lineSW620 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultTumor volume become 59.9% as compared to control 100% after day 19 | Mode of deliveryIntravenous | Pathway inducedInduction of necrosis and apoptosis in animal model cancer cell line | Immunogenic effectNA | Clinical trialNA | PMID28578522 |
IDOV_3498 | Virus nameAdenovirus | Virus strainAdenovirus CRAds | 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 lineCell collection centre china | Origin of cell lineHuman lung cancer cell line | Cell lineA549 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration8.0E+6 pfu | In-vivo toxicityNA | In-vivo resultTumor size regressed to 700mm compared to control 900mm after 65 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID28638457 |
IDOV_3499 | Virus nameAdenovirus | Virus strainAdenovirus CRAds | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with cisplatin | Immune gene insertion in viral genomeNo | Source of cell lineCell collection centre china | Origin of cell lineHuman lung cancer cell line | Cell lineA549 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration8.0E+6 pfu | In-vivo toxicityNA | In-vivo resultTumor size regressed to 100mm compared to control 900mm after 65 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID28638457 |
IDOV_3500 | Virus nameAdenovirus | Virus strainAdenovirus CRAds | 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 lineCell collection centre china | Origin of cell lineHuman lung cancer cell line | Cell lineA549-DDPR cisplatin resistant | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration8.0E+6 pfu | In-vivo toxicityNA | In-vivo resultTumor size regressed to 800mm compared to control 900mm after 65 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID28638457 |
IDOV_3501 | Virus nameAdenovirus | Virus strainAdenovirus CRAds | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationNone | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with cisplatin | Immune gene insertion in viral genomeNo | Source of cell lineCell collection centre china | Origin of cell lineHuman lung cancer cell line | Cell lineA549-DDPR cisplatin resistant | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for SW-620 cell line (1.0E+6) | In-vivo virus concentration8.0E+6 pfu | In-vivo toxicityNA | In-vivo resultTumor size regressed to 300mm compared to control 900mm after 65 days | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID28638457 |
IDOV_3520 | Virus nameAdenovirus | Virus strainAdenovirus ZD55-shMYCN | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationVirus expressing MYCN gene | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineLab own synthesized | Origin of cell lineHuman neuroblastoma cell line | Cell lineLA1-55n/Dox-R | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for LA1-55n/Dox-R cell line (2.0E+6) | In-vivo virus concentration7.0E+8 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed to 800mm after four week compared to normal 1400 mm. | Mode of deliveryNA | Pathway inducedInduction of apoptosis as measured by TUNEL assay | Immunogenic effectNA | Clinical trialNA | PMID28711493 |
IDOV_3521 | Virus nameAdenovirus | Virus strainAdenovirus ZD55-shMYCN | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationVirus expressing MYCN gene | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with Doxorubicin | Immune gene insertion in viral genomeNo | Source of cell lineLab own synthesized | Origin of cell lineHuman neuroblastoma cell line | Cell lineLA1-55n/Dox-R | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c nude mice xenograft for LA1-55n/Dox-R cell line (2.0E+6) | In-vivo virus concentration7.0E+8 pfu | In-vivo toxicityNA | In-vivo resultTumor volume regressed to 300mm after four week compared to normal 1400 mm. | Mode of deliveryNA | Pathway inducedInduction of apoptosis as measured by TUNEL assay | Immunogenic effectNA | Clinical trialNA | PMID28711493 |
IDOV_3618 | Virus nameAdenovirus | Virus strainAdenovirus CD55-TRAIL | Virus genome typeDNA | Virus familyAdenoviridae | Virus genome modificationVirus expressingTRAIL gene | Virus aloneNo | Virus in combination with drug/radiationVirus in combination with luteolin (50mg/kg) | Immune gene insertion in viral genomeNo | Source of cell lineShanghai cell collection | 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 organismBalb/c nude mice xenograft for HT29 cell line (8.0E+6) | In-vivo virus concentration2.0E+9 pfu | In-vivo toxicityNA | In-vivo resultDecrease in tumor volume to below 2000mm after 30 days comapred to control 4000mm | Mode of deliveryIntratumoral | Pathway inducedVirus in combination with induce apiptosis in cancer cell | Immunogenic effectNA | Clinical trialNA | PMID29039580 |
IDOV_3737 | Virus nameVesicular stomatitis virus | Virus strainVSV-GP | Virus genome typeRNA | Virus familyRhabdoviridae | Virus genome modificationvirus expressing GP protein | Virus aloneYes | Virus in combination with drug/radiationNo | Immune gene insertion in viral genomeNo | Source of cell lineATCC | Origin of cell lineHuman prostate cancer cell line | Cell lineDu145 | Concentration of cell lineNA | In-vitro toxicityNA | AssayNA | In-vitro virus concentrationNA | In-vitro resultNA | Model organismBalb/c-rag and gamma negative xenograft for Du145 (2.0E+6) | In-vivo virus concentration1.0E+7 pfu | In-vivo toxicityNA | In-vivo resultComplete regression in tumor after day 80 | Mode of deliveryIntratumoral | Pathway inducedNA | Immunogenic effectNA | Clinical trialNA | PMID29696636 |