Clinical trial
Vorinostat and Gemcitabine in Treating Patients With Metastatic or Unresectable…
NCT00243100 · National Cancer Institute (NCI), NIH · Completed
Key facts
| NCT number | NCT00243100 |
|---|---|
| Title | Vorinostat and Gemcitabine in Treating Patients With Metastatic or Unresectable Solid Tumors |
| Official title | A Phase 1 Study of Suberoylanilide Hydroxamic Acid (SAHA) in Combination With Gemcitabine in Patients With Epithelial Tumors |
| Lead sponsor | National Cancer Institute (NCI), NIH |
| Status | Completed |
| Phase | Phase 1 |
| Study type | Interventional |
| Conditions | Unspecified Adult Solid Tumor, Protocol Specific |
| Intervention type | Drug |
| Interventions | vorinostat, gemcitabine hydrochloride |
| Enrollment | 21 |
| Start date | Nov 1, 2005 |
| Primary completion | Aug 1, 2011 |
| First posted | Oct 21, 2005 |
| Last update posted | Dec 16, 2013 |
| 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: