Trials / Completed
CompletedNCT01183364
A Dose Escalation Study of STA-9090 and Docetaxel in Patients With Solid Tumors
A Phase 1, Pharmacokinetic Study of STA-9090 in Combination With Docetaxel in Subjects With Advanced Solid Tumor Malignancies
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 27 (actual)
- Sponsor
- Synta Pharmaceuticals Corp. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is an open-label, Phase 1, dose-escalation study to determine the recommended doses of STA-9090 (ganetespib) and docetaxel for the treatment of subjects with solid tumor malignancies. The safety and tolerability of the treatment will also be evaluated.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | STA-9090 (ganetespib) with Docetaxel | One treatment cycle will consist of weekly treatments for 2 weeks followed by a 1-week rest period. Treatment cycles will be repeated every 3 weeks. STA-9090 will be administered on Days 1 and 8 of each cycle and docetaxel will be administered on Day 1 of each cycle. Each agent will be administered as a separate 1-hour intravenous infusion. |
Timeline
- Start date
- 2010-07-01
- Primary completion
- 2013-03-01
- Completion
- 2013-05-01
- First posted
- 2010-08-17
- Last updated
- 2014-09-19
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01183364. Inclusion in this directory is not an endorsement.