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Completed Phase 2 Interventional Results available

Study of Oral Topotecan With Bevacizumab for Recurrent Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00698516

Public ClinicalTrials.gov record NCT00698516. 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 19, 2026, 9:38 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, Multicenter, Non-comparative, Phase II Study of Oral Topotecan in Combination With Bevacizumab for Second-line Treatment in Subjects With Relapsed Small-cell Lung Cancer (SCLC)

Brief summary

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

Combination of Hycamtin (topotecan) and Avastin (bevacizumab) could allow killing of both endothelial and neoplastic cells. We postulate that addition of bevacizumab to topotecan will increase delivery of topotecan to tumor cells and may enhance activity of topotecan in patients with previously treated small cell lung cancer and improve progression free survival.

Study identification

NCT ID
NCT00698516
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
50 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
Jul 2008 (Type not available)
Primary completion
May 2010 (Actual)
Completion
May 2010 (Actual)
Last update posted
Mar 27, 2012

2008 – 2010

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
GSK Investigational Site Jonesboro Arkansas 72401 —
GSK Investigational Site Gainesville Florida 32605 —
GSK Investigational Site Naples Florida 34119 —
GSK Investigational Site Athens Georgia 30607 —
GSK Investigational Site Macon Georgia 31201 —
GSK Investigational Site Marietta Georgia 30060 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site Cincinnati Ohio 45236 —
GSK Investigational Site Mt. Pleasant South Carolina 29464 —
GSK Investigational Site Chattanooga Tennessee 37404 —
GSK Investigational Site Memphis Tennessee 38104 —
GSK Investigational Site Memphis Tennessee 38120 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Seattle Washington 98101-2795 —
GSK Investigational Site Madison Wisconsin 53792 —

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 NCT00698516, 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 Mar 27, 2012 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00698516 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →