|
No. | NCT number | Interventions | Phases | Enrollment | Status | Outcome |
|
1 | NCT00395655 | Hydralazine and magnesium valproate | Phase 2 | 16 | Terminated | CR: 31% (5/16); PR: 50% (8/16) |
2 | NCT01194908 | Decitabine, LBH589, and tamoxifen | Phase 1, phase 2 | 5 | Terminated | No study results posted |
3 | NCT00567879 | Panobinostat and Trastuzumab | Phase 1, phase 2 | 56 | Terminated | PR: 1.78% (1/56) |
4 | NCT00777335 | Panobinostat and LBH589 | Phase 2 | 4 | Terminated | CR: 0; PR: 0 |
5 | NCT00132002 | Vorinostat | Phase 2 | 14 | Terminated | ORR: 0; mean OS: 24 months |
6 | NCT00262834 | Vorinostat | Phase 2 | 54 | Completed | Number of participants with AEs: 17/25 |
7 | NCT01118975 | Vorinostat and lapatinib | Phase 1, phase 2 | 12 | Terminated | No study results posted |
8 | NCT00828854 | Entinostat (SNDX-275) | Phase 2 | 25 | Completed | No study results posted |
9 | NCT00258349 | Vorinostat and trastuzumab | Phase 1, phase 2 | 16 | Completed | CR: 0; PR: 0; mean TTP: 1.5 months. Mean OS: 9.3 months |
10 | NCT00365599 | Vorinostat and tamoxifen | Phase 2 | 43 | Completed | ORR: 18.6% (8/43); mean TTP: 10.3 months. Number of participants with serious AEs: 4/43 |
11 | NCT00676663 | Entinostat and exemestane | Phase 2 | 64 | Completed | ORR: 4.7% |
12 | NCT01194427 | Vorinostat and tamoxifen | Phase 2 | 2 | Terminated | No study results posted |
13 | NCT00126451 | MK0683, vorinostat, and suberoylanilide hydroxamic acid (SAHA) | Phase 2 | 16 | Terminated | TTP: 33.5 days. Number of participants with serious AEs: 11/16 |
14 | NCT01105312 | Letrozole and panobinostat | Phase 1, phase 2 | 28 | Completed | CR: 0; PR: 0; mean survival time: 16.1 months; mean TTP: 2.1 months; PFS: 2.1 months; TTF: 2.1 months |
15 | NCT00368875 | Vorinostat, paclitaxel, and bevacizumab | Phase 1, phase 2 | 53 | Completed | CR: 4% (2/53); PR: 45% (24/53); mean PFS: 11.9 months; mean OS: 29.4 months; TTF: 0 |
16 | NCT01234532 | Entinostat and anastrozole | Phase 2 | 5 | Terminated | No study results posted |
17 | NCT00574587 | Vorinostat, paclitaxel, trastuzumab, doxorubicin, and cyclophosphamide | Phase 1, phase 2 | 55 | Completed | CR: 33.3% (17/51) |
18 | NCT00777049 | Panobinostat | Phase 2 | 54 | Completed | CR: (1.9%) 1/54; PR: (1.9%) 1/54 |
19 | NCT02395627 | Tamoxifen, vorinostat, and pembrolizumab | Phase 2 | 38 | Terminated | ORR: 6.67%; DoR: 17.0 months (group A), 8.8 months (group B); mean PFS: 2.57 months (group A), 2.63 months (group B); mean OS: 14.3 months (group A), 15.0 months (group B), and 7.8 months (group C) |
|