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Completed Phase 2 Interventional

Study Evaluating the Safety and Efficacy of MEGF0444A in Combination With Carboplatin, Paclitaxel and Bevacizumab in Patients With Advanced or Recurrent Non-Squamous Non-Small Cell Lung Cancer Who Have Not Received Prior Chemotherapy for Advanced Disease (NILE)

ClinicalTrials.gov ID: NCT01366131

Public ClinicalTrials.gov record NCT01366131. 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 Jul 21, 2026, 12:53 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 Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Safety and Efficacy of MEGF0444A in Combination With Carboplatin , Paclitaxel and Bevacizumab in Patients With Advanced or Recurrent Non-Squamous Non-Small Cell Lung Cancer Who Have Not Received Prior Chemotherapy for Advanced Disease

Study identification

NCT ID
NCT01366131
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genentech, Inc.
Industry
Enrollment
104 participants

Conditions and interventions

Interventions

  • MEGF0444A Drug
  • bevacizumab Drug
  • carboplatin Drug
  • paclitaxel Drug
  • placebo 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
May 31, 2011
Primary completion
Jan 31, 2013
Completion
Not listed
Last update posted
Nov 1, 2016

Started 2011

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
Not listed Birmingham Alabama 35205
Not listed Hot Springs Arkansas 71913
Not listed Santa Monica California 90404
Not listed Orlando Florida 32904
Not listed Port Saint Lucie Florida 34952
Not listed St. Petersburg Florida 33719
Not listed Tampa Florida 33603
Not listed Marietta Georgia 30060
Not listed Indianapolis Indiana 46260
Not listed Wichita Kansas 67214-3728
Not listed Burnsville Minnesota 55337
Not listed Las Vegas Nevada 89148
Not listed Albany New York 12208
Not listed Columbus Ohio 43219
Not listed Portland Oregon 97239
Not listed Hershey Pennsylvania 17033
Not listed Nashville Tennessee 37203
Not listed Austin Texas 78731
Not listed Fort Worth Texas 76104
Not listed 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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01366131, 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 1, 2016 · Synced Jul 21, 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 NCT01366131 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →