ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

An Open-label Study of GSK1120212 Compared With Docetaxel in Stage IV KRAS-mutant Non-small Cell Lung Cancer

ClinicalTrials.gov ID: NCT01362296

Public ClinicalTrials.gov record NCT01362296. 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 May 12, 2026, 3:43 AM 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 Phase II, Open-label, Multicenter, Randomized Study to Assess the Efficacy and Safety of GSK1120212 Compared With Docetaxel in 2nd Line Subjects With Targeted Mutations (KRAS, NRAS, BRAF, MEK1) in Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC Stage IV)

Study identification

NCT ID
NCT01362296
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
134 participants

Conditions and interventions

Interventions

  • GSK1120212 Drug
  • docetaxel Drug

Drug

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
Aug 31, 2011
Primary completion
Aug 31, 2012
Completion
Aug 31, 2013
Last update posted
Jul 10, 2014

2011 – 2013

United States locations

U.S. sites
25
U.S. states
21
U.S. cities
23
Facility City State ZIP Site status
GSK Investigational Site Scottsdale Arizona 85259
GSK Investigational Site Orange California 92868
GSK Investigational Site Aurora Colorado 80045
GSK Investigational Site Jacksonville Florida 32224
GSK Investigational Site Athens Georgia 30607
GSK Investigational Site Coeur d'Alene Idaho 83814
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site Baltimore Maryland 21231-2410
GSK Investigational Site Boston Massachusetts 02114
GSK Investigational Site Boston Massachusetts 02215
GSK Investigational Site Detroit Michigan 48201
GSK Investigational Site Minneapolis Minnesota 55404
GSK Investigational Site Rochester Minnesota 55905
GSK Investigational Site St Louis Missouri 63110
GSK Investigational Site Lebanon New Hampshire 03756
GSK Investigational Site Durham North Carolina 27710
GSK Investigational Site Columbus Ohio 43210
GSK Investigational Site Portland Oregon 97239
GSK Investigational Site Philadelphia Pennsylvania 19104
GSK Investigational Site Philadelphia Pennsylvania 19141
GSK Investigational Site Memphis Tennessee 38120
GSK Investigational Site Austin Texas 78731
GSK Investigational Site Houston Texas 77030
GSK Investigational Site Fairfax Virginia 22031
GSK Investigational Site Vancouver Washington 98684

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 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01362296, 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 Jul 10, 2014 · Synced May 12, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01362296 live on ClinicalTrials.gov.

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