Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study of Vandetanib Combined With Chemotherapy to Treat Advanced Non-small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00687297

Public ClinicalTrials.gov record NCT00687297. 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 27, 2026, 1:51 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 Randomized Phase II Study Evaluating Vandetanib (ZD6474) in Combination With Docetaxel and Carboplatin Followed by Placebo or Maintenance Therapy With Vandetanib in Patients With IIIb, IV or Recurrent Non-Small Cell Lung Cancer (NSCLC)

Brief summary

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

It has been shown in previous studies that the ability to treat lung cancer could be significantly improved by not only targeting the tumor cells directly with chemotherapy, but also by cutting off the blood supply to the cancer cells. Blood vessels that supply the tumor are formed through a process called angiogenesis. Vandetanib is an investigational drug that acts by producing what is called an anti-angiogenic effect. An Anti-angiogenic effect is able to inhibit the development of new blood vessels required by tumors to survive by blocking the growth factors needed to form new blood vessels. The purpose of this study is to determine if the addition of vandetanib to a standard chemotherapy regimen will slow or stop the growth of the cancer for a longer period of time compared to the time period generally gained from the use of standard chemotherapy alone

Study identification

NCT ID
NCT00687297
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
PrECOG, LLC.
Other
Enrollment
162 participants

Conditions and interventions

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
Apr 2008 (Type not available)
Primary completion
Jan 2011 (Actual)
Completion
Apr 2011 (Actual)
Last update posted
May 30, 2018

2008 – 2011

United States locations

U.S. sites
30
U.S. states
16
U.S. cities
29
Facility City State ZIP Site status
Boca Raton Community Hospital Boca Raton Florida 33486 —
Lakeland Regional Cancer Center Lakeland Florida 33805 —
SwedishAmerican Hospital Rockford Illinois 61104 —
Cancer Center of Kansas Wichita Kansas 67214 —
Ochsner Clinic New Orleans Louisiana 70121 —
Greater Baltimore Medical Center Baltimore Maryland 21204 —
St. Joseph Mercy Hospital- Ann Arbor Ann Arbor Michigan 48106 —
West Michigan Cancer Center Kalamazoo Michigan 49007 —
Metro-Minnesota CCOP Saint Louis Park Minnesota 55416 —
Ocean Medical Center Brick New Jersey 08724 —
Morristown Memorial Hospital Morristown New Jersey 07960 —
Cancer Institute of New Jersey New Brunswick New Jersey 08903 —
Riverview Medical Center Red Bank New Jersey 07701 —
Montefiore Medical Center The Bronx New York 10467 —
Aultman Hospital Canton Ohio 44710 —
Abington Memorial Hospital Abington Pennsylvania 19001 —
Hematology & Oncology of NEPA Dunmore Pennsylvania 18512 —
Lancaster General Hospital Lancaster Pennsylvania 17604 —
Central PA Hematology & Medical Oncology Associaties Lemoyne Pennsylvania 17043 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Albert Einstein Cancer Center Philadelphia Pennsylvania 19141 —
The Reading Hospital and Medical Center Reading Pennsylvania 19610 —
Mount Nittany Medical Center State College Pennsylvania 16803 —
Sanford Clinic Sioux Falls South Dakota 57104 —
Meharry Medical College Nashville Tennessee 37208 —
University of Texas Southwestern Medical Center Dallas Texas 75390 —
Charleston Area Medical Center Charleston West Virginia 25304 —
St. Vincent Hospital Green Bay Wisconsin 45301 —
Gundersen Lutheran La Crosse Wisconsin 54601 —
Regional Cancer Center Waukesha Wisconsin 53188 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00687297, 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 May 30, 2018 · Synced Oct 27, 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 public registry record, listed eligibility criteria, and available contact information for NCT00687297 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →