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Completed Phase 3 Interventional Results available

Phase III Study of Docetaxel + Ramucirumab or Placebo in Breast Cancer

ClinicalTrials.gov ID: NCT00703326

Public ClinicalTrials.gov record NCT00703326. 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 18, 2026, 8:23 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 Multicenter, Multinational, Randomized, Double-Blind, Phase III Study of IMC-1121B Plus Docetaxel Versus Placebo Plus Docetaxel in Previously Untreated Patients With HER2-Negative, Unresectable, Locally-Recurrent or Metastatic Breast Cancer

Brief summary

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

The objective of this study is to compare the progression-free survival (PFS) of the drug combination ramucirumab plus docetaxel to placebo plus docetaxel in previously untreated participants with human epidermal growth factor receptor 2 (HER2)-negative, unresectable, locally-recurrent or metastatic breast cancer.

Study identification

NCT ID
NCT00703326
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
1,144 participants

Conditions and interventions

Conditions

Interventions

Biological · Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Aug 6, 2008 (Actual)
Primary completion
Mar 31, 2013 (Actual)
Completion
Nov 19, 2020 (Actual)
Last update posted
Dec 6, 2021

2008 – 2020

United States locations

U.S. sites
65
U.S. states
24
U.S. cities
55
Facility City State ZIP Site status
ImClone Investigational Site Birmingham Alabama 35202 —
ImClone Investigational Site Mobile Alabama 36608 —
ImClone Investigational Site Chandler Arizona 85224 —
ImClone Investigational Site Gilbert Arizona 85297 —
ImClone Investigational Site Mesa Arizona 85206 —
ImClone Investigational Site Alhambra California 91801 —
ImClone Investigational Site Bakersfield California 93309 —
ImClone Investigational Site Chula Vista California 91911 —
ImClone Investigational Site La Mesa California 91942 —
ImClone Investigational Site Los Angeles California 90095 —
ImClone Investigational Site Oceanside California 92056 —
ImClone Investigational Site Pasadena California 01107 —
ImClone Investigational Site Pasadena California 91105 —
ImClone Investigational Site San Diego California 92123 —
ImClone Investigational Site Santa Barbara California 93105 —
ImClone Investigational Site Santa Maria California 93454 —
ImClone Investigational Site Santa Monica California 90404 —
ImClone Investigational Site Solvang California 93463 —
ImClone Investigational Site Valencia California 91355 —
ImClone Investigational Site Aurora Colorado 80045 —
ImClone Investigational Site Fort Lauderdale Florida 33308 —
ImClone Investigational Site Gainesville Florida 32605 —
ImClone Investigational Site New Port Richey Florida 34655 —
ImClone Investigational Site Atlanta Georgia 30341 —
ImClone Investigational Site Atlanta Georgia 30342 —
ImClone Investigational Site Macon Georgia 31217 —
ImClone Investigational Site Marietta Georgia 30060 —
ImClone Investigational Site Alton Illinois 62002 —
ImClone Investigational Site Chicago Illinois 60076 —
ImClone Investigational Site Chicago Illinois 60611 —
ImClone Investigational Site Skokie Illinois 60076 —
ImClone Investigational Site Elkhart Indiana 46514 —
ImClone Investigational Site Mishawaka Indiana 46545 —
ImClone Investigational Site South Bend Indiana 46601 —
ImClone Investigational Site Westville Indiana 46891 —
ImClone Investigational Site Lexington Kentucky 40604 —
ImClone Investigational Site Lansing Michigan 48912 —
ImClone Investigational Site Saint Joseph Michigan 49085 —
ImClone Investigational Site Minneapolis Minnesota 55415 —
ImClone Investigational Site Southaven Mississippi 38671 —
ImClone Investigational Site St Louis Missouri 63136 —
ImClone Investigational Site Grand Island Nebraska 68803 —
ImClone Investigational Site Kearney Nebraska 68845 —
ImClone Investigational Site Henderson Nevada 89052 —
ImClone Investigational Site New York New York 10011 —
ImClone Investigational Site Charlotte North Carolina 15830 —
ImClone Investigational Site Charlotte North Carolina 28203 —
ImClone Investigational Site Charlotte North Carolina 28210 —
ImClone Investigational Site Charlotte North Carolina 28211 —
ImClone Investigational Site Charlotte North Carolina 28262 —
ImClone Investigational Site Charlotte North Carolina 28294 —
ImClone Investigational Site Bismarck North Dakota 58501 —
ImClone Investigational Site Oklahoma City Oklahoma 73120 —
ImClone Investigational Site Portland Oregon 97239 —
ImClone Investigational Site West Reading Pennsylvania 19611 —
ImClone Investigational Site Bartlett Tennessee 38133 —
ImClone Investigational Site Germantown Tennessee 38138 —
ImClone Investigational Site Memphis Tennessee 38104 —
ImClone Investigational Site Memphis Tennessee 38119 —
ImClone Investigational Site Memphis Tennessee 38120 —
ImClone Investigational Site Niles Tennessee 49120 —
ImClone Investigational Site Oxford Tennessee 38655 —
ImClone Investigational Site Lubbock Texas 79410 —
ImClone Investigational Site Temple Texas 76508 —
ImClone Investigational Site Salt Lake City Utah 84106 —

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 167 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00703326, 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 6, 2021 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00703326 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →