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Completed Phase 2 Interventional

Study of Carboplatin/Paclitaxel in Combination With ABT-869 in Subjects With Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

ClinicalTrials.gov ID: NCT00716534

Public ClinicalTrials.gov record NCT00716534. 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 11, 2026, 9:13 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 2 Randomized, Placebo-Controlled, Double-Blind Study of Carboplatin/Paclitaxel in Combination With ABT-869 Versus Carboplatin/Paclitaxel Alone in Subjects With Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) as First-Line Treatment

Study identification

NCT ID
NCT00716534
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
145 participants

Conditions and interventions

Interventions

  • ABT-869 Drug
  • Carboplatin Drug
  • Paclitaxel Drug
  • Placebo for ABT-869 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, 2008
Primary completion
Mar 31, 2012
Completion
Mar 31, 2012
Last update posted
Apr 28, 2013

2008 – 2012

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Site Reference ID/Investigator# 15850 Chandler Arizona 85224
Site Reference ID/Investigator# 15846 Peoria Arizona 85381
Site Reference ID/Investigator# 15841 Miami Florida 33136
Site Reference ID/Investigator# 7179 Atlanta Georgia 30322
Site Reference ID/Investigator# 15851 Lansing Michigan 48912
Site Reference ID/Investigator# 15844 Lebanon New Hampshire 03756
Site Reference ID/Investigator# 22443 Hackensack New Jersey 07601
Site Reference ID/Investigator# 15848 Greensboro North Carolina 27403
Site Reference ID/Investigator# 22444 Canton Ohio 44718
Site Reference ID/Investigator# 15847 Cleveland Ohio 44195
Site Reference ID/Investigator# 26842 Hershey Pennsylvania 17033-0850
Site Reference ID/Investigator# 13101 Philadelphia Pennsylvania 19106
Site Reference ID/Investigator# 24122 Philadelphia Pennsylvania 19107

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00716534, 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 Apr 28, 2013 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00716534 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →