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Completed Phase 2 Interventional

Study of ABT-869 in Subjects With Advanced Non-small Cell Lung Cancer (NSCLC)

ClinicalTrials.gov ID: NCT00517790

Public ClinicalTrials.gov record NCT00517790. 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 Jun 25, 2026, 11:04 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

An Open-Label, Randomized, Phase 2 Study of Efficacy and Tolerability of ABT-869 in Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

Study identification

NCT ID
NCT00517790
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
140 participants

Conditions and interventions

Interventions

  • ABT-869 .25 mg/kg Drug
  • ABT-869 0.10 mg/kg 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
Jul 31, 2007
Primary completion
May 31, 2011
Completion
May 31, 2012
Last update posted
Apr 4, 2013

2007 – 2012

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Site Reference ID/Investigator# 7194 Fountain Valley California 92708
Site Reference ID/Investigator# 5617 Los Angeles California 90033
Site Reference ID/Investigator# 7934 Sacramento California 95817
Site Reference ID/Investigator# 5646 Aurora Colorado 80045-0510
Site Reference ID/Investigator# 6627 Waterbury Connecticut 06708
Site Reference ID/Investigator# 7868 Newark Delaware 19718
Site Reference ID/Investigator# 7616 Port Saint Lucie Florida 34952
Site Reference ID/Investigator# 5648 Chicago Illinois 60637
Site Reference ID/Investigator# 6739 Evanston Illinois 60201
Site Reference ID/Investigator# 8100 Harvey Illinois 60426
Site Reference ID/Investigator# 5269 Indianapolis Indiana 46202
Site Reference ID/Investigator# 6042 St Louis Missouri 63110
Site Reference ID/Investigator# 6680 East Orange New Jersey 07018
Site Reference ID/Investigator# 5603 Voorhees Township New Jersey 08043
Site Reference ID/Investigator# 5652 Buffalo New York 14263
Site Reference ID/Investigator# 6184 Charlotte North Carolina 28211
Site Reference ID/Investigator# 6777 Greensboro North Carolina 27403
Site Reference ID/Investigator# 5650 Memphis Tennessee 38120

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00517790, 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 4, 2013 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00517790 live on ClinicalTrials.gov.

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