ClinicalTrials.gov record
Terminated Phase 3 Interventional

First-Line Treatment for Locally Advanced or Metastatic Mesenchymal Epithelial Transition Factor (MET) - Positive Gastric, Lower Esophageal, or Gastroesophageal Junction (GEJ) Adenocarcinoma

ClinicalTrials.gov ID: NCT01697072

Public ClinicalTrials.gov record NCT01697072. 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 Apr 29, 2026, 12:17 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 3, Multicenter, Randomized, Double-Blind, Placebo Controlled Study of Rilotumumab (AMG102) With Epirubicin, Cisplatin, and Capecitabine (ECX) as First-line Therapy in Advanced MET-Positive Gastric or Gastroesophageal Junction Adenocarcinoma

Study identification

NCT ID
NCT01697072
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
609 participants

Conditions and interventions

Conditions

Interventions

  • Capecitabine Drug
  • Cisplatin Drug
  • Epirubicin Drug
  • Placebo Other
  • Rilotumumab Drug

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 99 Years
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 30, 2012
Primary completion
Oct 31, 2014
Completion
Jul 31, 2015
Last update posted
Feb 8, 2016

2012 – 2015

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Research Site Tucson Arizona 85724
Research Site Aurora Colorado 80045
Research Site Pueblo Colorado 81008
Research Site Chicago Illinois 60637
Research Site Baltimore Maryland 21231
Research Site Woodbury Minnesota 55125
Research Site Henderson Nevada 89052
Research Site New York New York 10065
Research Site Rochester New York 14642
Research Site Greensboro North Carolina 27403
Research Site Winston-Salem North Carolina 27103
Research Site Pittsburgh Pennsylvania 15232
Research Site Nashville Tennessee 37232
Research Site Bedford Texas 76022
Research Site Dallas Texas 75246
Research Site Seattle Washington 98109

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 173 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01697072, 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 Feb 8, 2016 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01697072 live on ClinicalTrials.gov.

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