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Completed Phase 2 Interventional

Safety and Efficacy of Single-agent CC-5013 in Subjects With Relapsed and Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT00065351

Public ClinicalTrials.gov record NCT00065351. 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 15, 2026, 12:04 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, Open-label Study to Determine the Safety and Efficacy of Single-agent CC-5013 in Subjects With Relapsed and Refractory Multiple Myeloma

Brief summary

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

For each subject the study will consist of two phases: a treatment phase and a follow-up phase. Screening procedures will take place within 28 days of baseline. Treatment Phase: Subjects who qualify for enrollment into the study will receive single-agent CC-5013 in 28-day cycles. Study visits will occur every 4 weeks and hematologic and myeloma paraprotein laboratory assessments will occur every 2 weeks for the first 6 cycles and every 4 weeks thereafter. Follow-Up Phase: All subjects who discontinue the treatment phase for any reason will continue to be followed for survival and post-treatment phase anti-myeloma treatment.

Study identification

NCT ID
NCT00065351
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celgene
Industry
Enrollment
222 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
Jul 1, 2003 (Actual)
Primary completion
Oct 1, 2006 (Actual)
Completion
Mar 1, 2007 (Actual)
Last update posted
Nov 12, 2019

2003 – 2007

United States locations

U.S. sites
26
U.S. states
14
U.S. cities
24
Facility City State ZIP Site status
Palo Verde Hematology Oncology Glendale Arizona 85304 —
Mayo Clinic Scottsdale Arizona 85259 —
Alta Bates Comprehensive Cancer Center Berkeley California 94704 —
Providence St. Joseph Medical Center/Cancer Center Burbank California 91505 —
Wilshire Oncology Medical Group, Inc. La Verne California 91750 —
Institute for Myeloma and Bone Los Angeles California 90067 —
Cancer Care Associates Redondo Beach California 90277 —
Mayo Clinic Jacksonville Florida 32224 —
Northwest Georgia Oncology Centers Marietta Georgia 30060 —
Atlanta Cancer Care-Roswell Roswell Georgia 30076 —
Northwestern University Med Ctr Chicago Illinois 60611-2927 —
Midwest Cancer Research Group Skokie Illinois 60077 —
University of Maryland Medical Center Baltimore Maryland 21201-1595 —
Center for Cancer and Blood Disorders Bethesda Maryland 20717 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Dana-Farber Cancer Institute Boston Massachusetts 02115 —
University of Massachusetts Worcester Massachusetts 01655 —
Mayo Clinic Rochester Minnesota 55902 —
Nevada Cancer Center Las Vegas Nevada 89109 —
SUNY Health Science Center at Brooklyn Brooklyn New York 11203 —
St. Vincent's Comprehensive Cancer Center New York New York 10011 —
Carolina Hematology-Oncology Associates Charlotte North Carolina 28203 —
Cleveland Clinic Myeloma Program Hematology & Medical Oncology /R35 Cleveland Ohio 44195 —
Western Pennsylvania Cancer Institute Pittsburgh Pennsylvania 15224 —
Swedish Cancer Institute Seattle Washington 98104 —
Fred Hutchinson Cancer Research Center Seattle Washington 98109-1024 —

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 NCT00065351, 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 Nov 12, 2019 · Synced Oct 15, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00065351 live on ClinicalTrials.gov.

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