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Completed Phase 2 Interventional Results available

A Study of IMC-A12 or Ramucirumab Plus Mitoxantrone and Prednisone in Prostate Cancer

ClinicalTrials.gov ID: NCT00683475

Public ClinicalTrials.gov record NCT00683475. 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 17, 2026, 9:16 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, Multicenter, Randomized Study of IMC-A12 or IMC-1121B Plus Mitoxantrone and Prednisone in Metastatic Androgen-Independent Prostate Cancer (AIPC) Following Disease Progression on Docetaxel-Based Chemotherapy

Brief summary

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

The purpose of this study is to determine whether IMC-A12 or IMC-1121B (ramucirumab) with Mitoxantrone and Prednisone is effective in the treatment of metastatic androgen- independent prostate cancer (APIC).

Study identification

NCT ID
NCT00683475
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
138 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
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 2008 (Type not available)
Primary completion
Sep 2011 (Actual)
Completion
Sep 2011 (Actual)
Last update posted
Oct 16, 2014

2008 – 2011

United States locations

U.S. sites
36
U.S. states
21
U.S. cities
31
Facility City State ZIP Site status
ImClone Investigational Site La Jolla California 92093 —
ImClone Investigational Site New Haven Connecticut 06520 —
ImClone Investigational Site Boca Raton Florida 33486 —
ImClone Investigational Site Port Saint Lucie Florida 34952 —
ImClone Investigational Site Atlanta Georgia 30318 —
ImClone Investigational Site Chicago Illinois 60611 —
ImClone Investigational Site Chlcago Illinois 60637 —
ImClone Investigational Site Evanston Illinois 60201 —
ImClone Investigational Site Maryville Illinois 62062 —
ImClone Investigational Site Cedar Rapids Iowa 52402 —
ImClone Investigational Site Metairie Louisiana 70006 —
ImClone Investigational Site Ann Arbor Michigan 48109 —
ImClone Investigational Site Rochester Minnesota 55905 —
ImClone Investigational Site St Louis Missouri 63110 —
ImClone Investigational Site Billings Montana 59101 —
ImClone Investigational Site Roseland New Jersey 07068 —
ImClone Investigational Site Buffalo New York 14263 —
ImClone Investigational Site East Setauket New York 11733 —
ImClone Investigational Site New York New York 10016 —
ImClone Investigational Site New York New York 10019 —
ImClone Investigational Site New York New York 10021 —
ImClone Investigational Site New York New York 10032 —
ImClone Investigational Site Durham North Carolina 27710 —
ImClone Investigational Site Cleveland Ohio 44195 —
ImClone Investigational Site Philadelphia Pennsylvania 19111 —
ImClone Investigational Site Pittsburgh Pennsylvania 15232 —
ImClone Investigational Site Greenville South Carolina 29605 —
ImClone Investigational Site Knoxville Tennessee 37920 —
ImClone Investigational Site Nashville Tennessee 37203 —
ImClone Investigational Site Abilene Texas 79606 —
ImClone Investigational Site Dallas Texas 75246 —
ImClone Investigational Site Houston Texas 77030-4009 —
ImClone Investigational Site Houston Texas 77030 —
ImClone Investigational Site Seattle Washington 98104 —
ImClone Investigational Site Seattle Washington 98109 —
ImClone 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 NCT00683475, 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 Oct 16, 2014 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00683475 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →