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Completed Phase 3 Interventional Results available

A Study of Bevacizumab in Combination With Capecitabine and Cisplatin as First-line Therapy in Patients With Advanced Gastric Cancer

ClinicalTrials.gov ID: NCT00548548

Public ClinicalTrials.gov record NCT00548548. 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 22, 2026, 5:17 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 Double-blind, Randomised, Multicenter, Phase III Study of Bevacizumab in Combination With Capecitabine and Cisplatin Versus Placebo in Combination With Capecitabine and Cisplatin, as First-line Therapy in Patients With Advanced Gastric Cancer

Brief summary

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

This study will compare treatment with bevacizumab in combination with capecitabine and cisplatin versus placebo in combination with capecitabine and cisplatin, as first-line therapy in patients with locally advanced or metastatic gastric cancer who had not received prior chemotherapy for advanced or metastatic disease.

Study identification

NCT ID
NCT00548548
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Genentech, Inc.
Industry
Enrollment
774 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
Sep 2007 (Actual)
Primary completion
Nov 2009 (Actual)
Completion
Nov 2013 (Actual)
Last update posted
Jun 14, 2017

2007 – 2013

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Tower Cancer Research Fnd Beverly Hills California 90211-1850 —
Moores UCSD Cancer Center La Jolla California 92093 —
Kenmar Research Institute LLC Los Angeles California 90057 —
USC/Norris Cancer Center Los Angeles California 90089 —
Georgetown University Washington D.C. District of Columbia 20007 —
Florida Cancer Specialists Fort Myers Florida 33916 —
H. Lee Moffitt Cancer Tampa Florida 33612 —
Cancer Center of Kansas Wichita Kansas 67214-3728 —
Methodist Cancer Center Onc Omaha Nebraska 68114 —
Memorial Sloan Kettering New York New York 10021 —
Duke Univ Medical Center Durham North Carolina 27710 —
South Carolina Oncology Assoc Columbia South Carolina 10595 —
The Sarah Cannon Research Inst Nashville Tennessee 37203 —

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 NCT00548548, 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 Jun 14, 2017 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00548548 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →