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Terminated Phase 2Phase 3 Interventional

Study of Ganetespib (STA-9090) + Docetaxel in Advanced Non Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT01348126

Public ClinicalTrials.gov record NCT01348126. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 6:32 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Phase IIB/III Study of Ganetespib (STA-9090) in Combination With Docetaxel Versus Docetaxel Alone in Subjects With Stage IIIb or IV Non-Small-Cell Lung Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 subjects with advanced non-small cell lung cancer.

Study identification

NCT ID
NCT01348126
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Synta Pharmaceuticals Corp.
Industry
Enrollment
385 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2011 (Type not available)
Primary completion
Apr 2014 (Actual)
Completion
Oct 2015 (Actual)
Last update posted
Nov 5, 2015

2011 – 2015

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Synta Pharmaceuticals Investigative Site Tucson Arizona 85715 —
Synta Pharmaceuticals Investigative Site Santa Monica California 90404 —
Synta Pharmaceuticals Investigative Site Atlanta Georgia 30322 —
Synta Pharmaceuticals Investigative Site Chicago Illinois 60637 —
Synta Pharmaceutials Investigative Site Boston Massachusetts 02215 —
Synta Pharmaceuticals Investigative Site Winston-Salem North Carolina 27103 —
Synta Pharmaceuticals Investigative Site Kettering Ohio 45429 —
Synta Pharmaceuticals Investigative Site Portland Oregon 97227 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01348126, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 5, 2015 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01348126 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →