Table 3.
Clinical trials of HDACi and Pt drugs combination therapy
| HDACi | Cancer target | Purpose | Gov. registration # | Patient population | Results | Clinical phase |
|---|---|---|---|---|---|---|
| SAHA (CDDP+Capecitabine) | Metastatic or Recurrent Gastric Cancer | Exploring the role of SAHA | NCT01045538 | 45 | CR | I/II |
| VPA(Hydralazine) | Cervical cancer | Determining response rate, safety, biological effects | NCT00404326 | 17 | Completed | II |
| Belinostat (CDDP+Etoposide) | Small cell lung carcinoma | Determining a safe, tolerable phase II dose | NCT00926640 | 39 | CR | I |
| CUDC-101 (CDDP) | Head and neck | A dose escalation study | NCT01384799 | 22 | CR | I |
| SAHA | Non-small cell lung cancer (non-SCLC) | determining the maximum tolerated dose | NCT01059552 | 22 | CR | I |
| SAHA(CDDP+Isotrti noin+Combined chemotherapy) | Embryonal tumors (Brain and Central Nervous System Tumors) | Side effects of giving SAHA isotretino in together with chemotherapy | NCT00867178 | 62 | CR | I |
| SAHA(CDDP+ Pemetrexed) | Advanced solid tumors | safety and tolerability | NCT00106626 | 52 | Safety issues: Yes | I |
| MK0683 (CDDP+Gemcitabine) | Non-SCLC | safety and tolerability | NCT00423449 | 61 | MTD 400 mg for up to 10 days in 21- day cycles Safety issues: Yes | I |
Ref source: Clinicaltrials.gov
CDDP: Cisplatin, CR: Current, MTD: Maximum tolerated dose, SCLC: Small cell lung cancer