Table 2.
Clinical Trials of DNA vaccines in cancer immunotherapy
NCT Number | Indication | Encoded protein | Adjuvant/Additional intervention | Strategy for breaking immune tolerance | Trial phase |
---|---|---|---|---|---|
aNCT02241369 | Aerodigestive Malignancies (e.g., Squamous Cell Carcinoma) | HPV6 E6 and E7 | IL-12 DNA | Tumor-specific viral antigen | I |
NCT02204098 | Breast cancer | Mammaglobin-A | Neoadjuvant Endocrine Therapy | Tumor-specific antigen | I |
NCT02348320 | Triple negative breast cancer | Personalized Antigenic Peptide | N/A | Tumor-specific antigen | I |
NCT02172911 | Cervical cancer | HPV16/18 E6 and E7 | IL-12 DNA | Tumor-specific viral antigen | I |
NCT01304524 | Cervical intraepithelial neoplasia | HPV16/18 E6 and E7 | N/A | Tumor-specific viral antigen | II |
NCT02596243 | Cervical intraepithelial neoplasia | HPV16/18 E6/E7 –FLT3L fusion | Built-in genetic adjuvant FLT3L | Tumor-specific viral antigen | II |
NCT01064375 | Colorectal cancer | CEA-tetanus toxoid fusion | GM-CSF adjuvant | Associative recognition | I/II |
NCT01493154 | Head and neck cancer | HPV E7-Calreticulin (CRT) fusion | Built-in genetic adjuvant CRT | Tumor-specific viral antigen | I |
NCT02163057 | Head and Neck squamous cell cancer | HPV16/18 E6/E7 | IL12 DNA | Tumor-specific viral antigen | I/II |
NCT01334060 | Acute and chronic Myeloid Leukemia (AML, CML) | WT1-DOM fusion protein | N/A | Associative recognition | II |
NCT01138410 | Malignant melanoma (Stage III/IV) | SCB1 | N/A | Associative recognition | I/II |
NCT00471133 | Skin and intraocular melanoma (Stage IIIB, IIC, III or IV) | Mouse tyrosinase | N/A | Xenogeneic antigen | |
NCT01440816 | Merkel cell carcinoma | IL12 | N/A | None | II |
NCT00859729 | Prostate cancer | rhesus PSA | N/A | Xenogeneic antigen | I/II |
NCT02514213 | Prostate cancer | PSA and PSMA | IL12 DNA | SynConTM antigen | I |
NCT02327468 | Multiple solid tumors | Human TERT | IL12 DNA | Antigen with modificationsb | I |
aNCT: National Clinical Trial
bThe TERT antigen encoded by the DNA vaccine was synthesized and codon-optimized. Two immunogenic mutations (R589Y and D1005Y) were incorporated into the hTERT sequence to assist in breaking tolerance