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Completed Phase 3 Interventional Results available

CC-5013 Plus Dexamethasone Versus Dexamethasone Alone in Previously Treated Subjects With Multiple Myeloma

ClinicalTrials.gov ID: NCT00056160

Public ClinicalTrials.gov record NCT00056160. 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, 4:36 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 Multicenter, Randomized, Parallel-Group, Double-blind, Placebo-controlled Study of CC-5013 Plus Dexamethasone Versus Dexamethasone Alone in Previously Treated Subjects With Multiple Myeloma

Brief summary

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

Randomized subjects will receive CC-5013 plus high-dose dexamethasone or placebo appearing identical to CC-5013 plus high-dose dexamethasone in 4-week cycles. Each subject will participate in a treatment phase and a follow-up phase.

Study identification

NCT ID
NCT00056160
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Celgene
Industry
Enrollment
353 participants

Conditions and interventions

Interventions

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
Jan 1, 2003 (Actual)
Primary completion
Nov 1, 2005 (Actual)
Completion
Oct 1, 2008 (Actual)
Last update posted
Oct 19, 2017

2003 – 2008

United States locations

U.S. sites
44
U.S. states
24
U.S. cities
41
Facility City State ZIP Site status
Clinical Research Consultants, Inc. Hoover Alabama 35216 —
City of Hope National Medical Center Duarte California 91010 —
UCLA School of Medicine Los Angeles California 90095 —
UCSF California San Francisco California 94143 —
Stanford University Medical Center, Division of Hematology Stanford California 94305-5112 —
Yale University School of Medicine New Haven Connecticut 06520 —
University of Florida Gainesville Florida 32610 —
Mayo Clinic- Jacksonville Jacksonville Florida 32224 —
University of Miami Miami Florida 33136 —
Oncology Hematology Consultants Sarasota Florida 34239 —
H Lee Moffitt Cancer Center Tampa Florida 33612-9497 —
Emory University Atlanta Georgia 30322 —
Medical College of Georgia Augusta Georgia 30912-3125 —
Northwestern University Med Ctr Chicago Illinois 60611-2927 —
Rush Cancer Institute Section of Hematology Chicago Illinois 60612-3824 —
Loyola University Medical Center Maywood Illinois 60153 —
Indiana Cancer Research Institute Indianapolis Indiana 46202-5254 —
University of Iowa Hospital Clinic Iowa City Iowa 52242 —
Ocshner Clinical Foundation New Orleans Louisiana 70121 —
Johns Hopkins Medicine Department of Oncology Baltimore Maryland 21231 —
Dana Farber Cancer Institute Boston Massachusetts 02115 —
University Of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109 —
Karmanos Cancer Institute Detroit Michigan 48201 —
Mayo Clinic Cancer Center Rochester Minnesota 55905 —
Washington University School of Medicine- Sherman Cancer Center St Louis Missouri 63110 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
Roswell Park Cancer Institute Buffalo New York 14263 —
St. Vincent's Comprehensive Cancer Center New York New York 10011 —
New York Presbyterian Hospital New York New York 10021 —
SUNY Upstate Medical University Syracuse New York 13210 —
MBCCOP Our Lady of Mercy Cancer Center New York Medical College The Bronx New York 10466 —
Duke University Medical Center Durham North Carolina 27710 —
Wake Forest University School of Medicine Winston-Salem North Carolina 27157-1023 —
Cleveland Clinic Myeloma Program Cleveland Ohio 44195 —
Ohio State University Columbus Ohio 43210 —
Kaiser Permanente Northwest Region Center for Health Research Portland Oregon 97227 —
University of Pennsylvania Cancer Center Philadelphia Pennsylvania 19104 —
University of Pittsburgh Pittsburgh Pennsylvania 15213 —
Charleston Hematology/Oncology P.A. Charleston South Carolina 29403 —
Medical University of SC Charleston South Carolina 29425 —
South Carolina Oncology Group West Columbia South Carolina 29169 —
Sarah Cannon Cancer Center Nashville Tennessee 37203-1632 —
MD Anderson Cancer Center Houston Texas 77030-4009 —
Froedtert Hospital/BMT Medical College of Wisconsin Milwaukee Wisconsin 53226-3522 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00056160, 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 19, 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 NCT00056160 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →