First-line Treatment of Patients With Stage IV Nonsquamous Non-Small Cell Lung Cancer With Necitumumab (IMC-11F8) and Pemetrexed-Cisplatin

NCT00982111 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 633

Last updated 2022-01-11

Study results available
· View outcomes & findings →

Summary

The research study is testing the investigational drug necitumumab in the treatment of advanced non-small cell lung cancer. The aim of this study is to determine if necitumumab, given together with a standard chemotherapy combination consisting of cisplatin and pemetrexed will be more effective in improving participant disease than the standard chemotherapy combination alone.

Conditions

  • Non Small Cell Lung Cancer

Interventions

DRUG

Pemetrexed

500 milligram per square meter (mg/m2) administered Intravenously (I.V.) on Day 1 of every 3-week cycle, for a maximum of six cycles

DRUG

Cisplatin

75 mg/m2 administered I.V. on Day 1 of every 3-week cycle, for a maximum of six cycles

BIOLOGICAL

Necitumumab

800 mg (absolute dose) on Days 1 and 8 of every 3-week cycle, administered as an I.V.

Sponsors & Collaborators

  • Quintiles, Inc.

    collaborator INDUSTRY
  • Parexel

    collaborator INDUSTRY
  • PPD Development, LP

    collaborator INDUSTRY
  • Medidata Solutions

    collaborator INDUSTRY
  • Laboratory Corporation of America

    collaborator INDUSTRY
  • University of Colorado, Denver

    collaborator OTHER
  • Thermo Fisher Scientific, Inc

    collaborator INDUSTRY
  • Pacific Biomarkers

    collaborator OTHER
  • Intertek

    collaborator INDUSTRY
  • Sysmex Inostics GmbH

    collaborator INDUSTRY
  • Eli Lilly and Company

    lead INDUSTRY

Principal Investigators

  • Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) · Eli Lilly and Company

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-02
Primary Completion
2012-11-14
Completion
2020-12-23

Countries

  • United States
  • Australia
  • Austria
  • Belgium
  • Brazil
  • Canada
  • Croatia
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Poland
  • Portugal
  • Romania
  • Russia
  • Slovakia
  • South Africa
  • Spain
  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00982111 on ClinicalTrials.gov