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|Therapy Name||Ad-MAGEA3 + MG1-MAGEA3 + Pembrolizumab|
|Drug Name||Trade Name||Synonyms||Drug Classes||Drug Description|
|Ad-MAGEA3||Adenovirus MAGE-A3|AdMA3|MAGE-A3-expressing Adenovirus Type 5 Vaccine||Ad-MAGEA3 is a cancer vaccine comprising a replication-defective adenovirus engineered to express MAGE-A3, which may result in enhanced immune response against MAGE-A3 expressing tumors (NCI Drug Dictionary).|
|MG1-MAGEA3||MG1-MAGEA3 is a cancer vaccine comprising an oncolytic Maraba virus strain expressing MAGEA3, which may result in enhanced immune response against cells expressing the tumor-associated antigen (TAA) MAGEA3 (PMID: 30546947).|
|Pembrolizumab||Keytruda||MK-3475||Immune Checkpoint Inhibitor 94 PD-L1/PD-1 antibody 65||Keytruda (pembrolizumab) is an antibody against PD-1 that activates T-cell mediated anti-tumor immune response (PMID: 25977344). Keytruda (pembrolizumab) is approved in melanoma, SCLC, HNSCC, classical Hodgkin Lymphoma, primary mediastinal large B-cell lymphoma, urothelial carcinoma, HCC, Merkel cell carcinoma, NMIBC, cutaneous squamous cell carcinoma, MSI-H or dMMR or TMB high advanced solid tumors, PD-L1 expressing NSCLC, gastric and GEJ adenocarcinoma, squamous esophageal carcinoma, and cervical cancer, in combination with pemetrexed and platinum in non-squamous NSCLC with no EGFR or ALK mutations, with carboplatin and paclitaxel/nab-paclitaxel in squamous NSCLC, with axitinib in RCC, and with Lenvatinib in endometrial carcinoma that is not MSI-H or dMMR (FDA.gov).|
|Molecular Profile||Indication/Tumor Type||Response Type||Therapy Name||Approval Status||Evidence Type||Efficacy Evidence||References|
|Clinical Trial||Phase||Therapies||Title||Recruitment Status|
|NCT02879760||Phase Ib/II||Ad-MAGEA3 + MG1-MAGEA3 + Pembrolizumab||Oncolytic MG1-MAGEA3 With Ad-MAGEA3 Vaccine in Combination With Pembrolizumab for Non-Small Cell Lung Cancer Patients||Active, not recruiting|