Clinical Trials Directory

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

TypeNameDescription
DRUGSTA-9090 (ganetespib) with DocetaxelOne 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.