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Active, not recruiting Phase 3 Interventional Results available

Assess Efficacy & Safety of Selumetinib in Combination With Docetaxel in Patients Receiving 2nd Line Treatment for v-Ki-ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) Positive NSCLC

ClinicalTrials.gov ID: NCT01933932

Public ClinicalTrials.gov record NCT01933932. 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 21, 2026, 1:54 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 III, Double-Blind, Randomised, Placebo-Controlled Study to Assess the Efficacy and Safety of Selumetinib (AZD6244; ARRY-142886) (Hyd-Sulfate) in Combination With Docetaxel, in Patients Receiving Second Line Treatment for KRAS Mutation-Positive Locally Advanced or Metastatic Non Small Cell Lung Cancer (Stage IIIB - IV) (SELECT 1)

Brief summary

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

The purpose of this study is to assess the efficacy of selumetinib in combination with docetaxel (75mg/m2) vs placebo in combination with docetaxel (75mg/m2) in patients with locally advance or metastatic NSCLCs that harbor mutations of KRAS. This study will also assess the PK, safety, patient reported outcomes (PRO) and tolerability profile of the selumetinib/docetaxel combination, compared to placebo in combination with docetaxel

Study identification

NCT ID
NCT01933932
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
510 participants

Conditions and interventions

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
Sep 25, 2013 (Actual)
Primary completion
Jun 7, 2016 (Actual)
Completion
Dec 31, 2026 (Estimated)
Last update posted
Jul 21, 2026

2013 – 2026

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Research Site Aurora Colorado 80045 —
Research Site Pembroke Pines Florida 33028 —
Research Site Atlanta Georgia 30318 —
Research Site Chicago Illinois 60637 —
Research Site Metairie Louisiana 70006 —
Research Site Boston Massachusetts 02114 —
Research Site Boston Massachusetts 02215 —
Research Site Danvers Massachusetts 01923 —
Research Site New York New York 10011 —
Research Site New York New York 10032 —
Research Site Durham North Carolina 27710 —
Research Site Hershey Pennsylvania 17033 —
Research Site Philadelphia Pennsylvania 19107 —
Research Site Nashville Tennessee 37203 —
Research Site Nashville Tennessee 37232 —
Research Site Seattle Washington 98104 —
Research Site Morgantown West Virginia 26506 —

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 180 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01933932, 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 21, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01933932 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →