Clinical trial
Safety of LBH589 Alone and in Combination With IV Docetaxel and Prednisone
NCT00493766 · Novartis Pharmaceuticals, Industry · Terminated
Key facts
| NCT number | NCT00493766 |
|---|---|
| Title | Safety of LBH589 Alone and in Combination With IV Docetaxel and Prednisone |
| Official title | A Phase IA/IB, Two Arm, Multi-center, Open-label, Dose Escalation Study of Oral LBH589 Alone and in Combination With IV Docetaxel and Oral Prednisone in Hormone Refractory Prostate Cancer (HRPC) |
| Lead sponsor | Novartis Pharmaceuticals, Industry |
| Status | Terminated |
| Phase | Phase 1 |
| Study type | Interventional |
| Conditions | Hormone Refractory Prostate Cancer |
| Intervention type | Drug |
| Interventions | LBH589 |
| Enrollment | 16 |
| Start date | May 1, 2006 |
| Primary completion | Jul 1, 2008 |
| First posted | Jun 28, 2007 |
| Last update posted | Dec 19, 2020 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: