A Phase 3 Study of Ganetespib in Combination With Docetaxel Versus Docetaxel Alone in Patients With Advanced NSCLC
NCT01798485 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 696
Last updated 2016-07-01
Summary
The purpose of this study is to determine whether combining ganetespib (STA-9090) with docetaxel is more effective than docetaxel alone in the treatment of patients with advanced non-small cell lung cancer.
Conditions
- Non-Small-Cell Lung Adenocarcinoma
- Non-small Cell Lung Cancer Stage IIIB
- Non-small Cell Lung Cancer Stage IV
- Non-small Cell Lung Cancer Metastatic
Interventions
- DRUG
-
Docetaxel, 75 mg/m\^2, was administered according to prevailing practice and Investigator decision, generally until disease progression, intolerability, or patient's withdrawal of consent.
- DRUG
-
Ganetespib
Ganetespib, 150 mg/m\^2, was administered with docetaxel. After docetaxel treatment ceased, participants whose disease has not progressed continued to receive ganetespib alone until disease progression, unacceptable toxicity, or patient's withdrawal of consent.
Sponsors & Collaborators
-
Synta Pharmaceuticals Corp.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-04-30
- Primary Completion
- 2015-12-31
- Completion
- 2015-12-31
Countries
- United States
- Austria
- Belgium
- Bosnia and Herzegovina
- Canada
- Croatia
- Czechia
- France
- Germany
- Hungary
- Italy
- Netherlands
- Poland
- Romania
- Russia
- Serbia
- Slovenia
- Spain
- Ukraine
- United Kingdom
Study Locations
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