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Completed Phase 2 Interventional Results available

Assess Efficacy and Safety of AZD6244 in Combination With Docetaxel in Patients Receiving Second Line Non Small Cell Lung Cancer Treatment.

ClinicalTrials.gov ID: NCT01750281

Public ClinicalTrials.gov record NCT01750281. 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 10, 2026, 1:34 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, Double-Blind, Randomised, Placebo-Controlled Study to Assess the Efficacy and Safety of Selumetinib (AZD6244; ARRY-142886) (Hyd-Sulfate) in Combination With Docetaxel, Compared With Placebo in Combination With Docetaxel, in Patients Receiving Second Line Treatment for Locally Advanced or Metastatic Non Small Cell Lung Cancer (Stage IIIB - IV)

Study identification

NCT ID
NCT01750281
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
212 participants

Conditions and interventions

Interventions

  • Docetaxel 60 mg/m2 Drug
  • Docetaxel 75 mg/m2 Drug
  • Placebo Drug
  • Selumetinib 75 mg Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 130 Years
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
Dec 17, 2012
Primary completion
Jan 26, 2016
Completion
Oct 30, 2022
Last update posted
Oct 23, 2023

2012 – 2022

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Research Site Santa Monica California 90404
Research Site Aurora Colorado 80045
Research Site Hollywood Florida 33028
Research Site Atlanta Georgia 30318
Research Site Chicago Illinois 60637
Research Site Marrero Louisiana 70072
Research Site Boston Massachusetts 02215
Research Site Mineola New York 11501
Research Site New York New York 10011
Research Site New York New York 10032
Research Site Hershey Pennsylvania 17033-0850
Research Site Philadelphia Pennsylvania 19107
Research Site Nashville Tennessee 37203

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 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01750281, 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 Oct 23, 2023 · Synced May 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01750281 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →