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Completed Phase 2 Interventional Results available

Study of GSK1363089 in Metastatic Gastric Cancer

ClinicalTrials.gov ID: NCT00725712

Public ClinicalTrials.gov record NCT00725712. 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 Sep 23, 2026, 11:08 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 Study of GSK1363089 (XL880) Administered Orally to Subjects With Metastatic Gastric Cancer

Brief summary

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

This clinical study is being conducted at multiple sites to determine the best confirmed response rate, safety, and tolerability of GSK1363089 treatment in metastatic gastric carcinoma.

Study identification

NCT ID
NCT00725712
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
74 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
Mar 30, 2007
Primary completion
Oct 31, 2009
Completion
Nov 29, 2009
Last update posted
Aug 23, 2017

2007 – 2009

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
16
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294
GSK Investigational Site Scottsdale Arizona 85258
GSK Investigational Site Los Angeles California 90024
GSK Investigational Site Stanford California 94305
GSK Investigational Site Washington D.C. District of Columbia 20007
GSK Investigational Site Atlanta Georgia 30309
GSK Investigational Site Chicago Illinois 60637
GSK Investigational Site Boston Massachusetts 02114
GSK Investigational Site Detroit Michigan 48201
GSK Investigational Site Billings Montana 59101
GSK Investigational Site Albuquerque New Mexico 87131
GSK Investigational Site New York New York 10016
GSK Investigational Site New York New York 10021
GSK Investigational Site Durham North Carolina 27710
GSK Investigational Site Portland Oregon 97239
GSK Investigational Site Austin Texas 78705
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 NCT00725712, 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 Aug 23, 2017 · Synced Sep 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00725712 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →