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

A Phase II Study of GSK1363089 (Formerly XL880) for Papillary Renal-Cell Carcinoma (PRC)

ClinicalTrials.gov ID: NCT00726323

Public ClinicalTrials.gov record NCT00726323. 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 Jul 21, 2026, 7:06 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 Phase II Study of the c-MET RTK Inhibitor XL880 in Subjects With Papillary Renal-Cell Carcinoma

Study identification

NCT ID
NCT00726323
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
74 participants

Conditions and interventions

Interventions

  • foretinib (formerly GSK1363089 or XL880) 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
Jun 29, 2006
Primary completion
Aug 17, 2010
Completion
Aug 17, 2010
Last update posted
Dec 10, 2017

2006 – 2010

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
GSK Investigational Site Greenbrae California 94904-2007
GSK Investigational Site San Francisco California 94115
GSK Investigational Site Stanford California 94305
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site Bethesda Maryland 20892
GSK Investigational Site Boston Massachusetts 02115
GSK Investigational Site Detroit Michigan 48201
GSK Investigational Site New Brunswick New Jersey 08901
GSK Investigational Site Cleveland Ohio 44195
GSK Investigational Site Philadelphia Pennsylvania 19104
GSK Investigational Site Nashville Tennessee 37232
GSK Investigational Site San Antonio Texas 78229

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 NCT00726323, 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 Dec 10, 2017 · Synced Jul 21, 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 protocol, eligibility criteria, and contact information for NCT00726323 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →