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Completed Phase 1Phase 2 Interventional Results available

MTD, Safety, and Efficacy of Pomalidomide (CC-4047) Alone or With Low-dose Dexamethasone in Patients With Relapsed and Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT00833833

Public ClinicalTrials.gov record NCT00833833. 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 Sep 5, 2026, 2:36 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 Phase I/II Multicenter, Randomized, Open Label, Dose-Escalation Study To Determine The Maximum Tolerated Dose, Safety, And Efficacy Of CC-4047 Alone Or In Combination With Low-Dose Dexamethasone In Patients Wth Relapsed And Refractory Multiple Myeloma Who Have Received Prior Treatment That Includes Lenalidomide And Bortezomib

Brief summary

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

The purpose of this study is to determine the maximum tolerated dose and effectiveness of the study drug (CC-4047) Alone Or in Combination With Low-dose Dexamethasone as treatment for patients with relapsed and refractory multiple myeloma

Study identification

NCT ID
NCT00833833
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Celgene Corporation
Industry
Enrollment
259 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
May 31, 2008
Primary completion
Mar 31, 2011
Completion
Aug 31, 2015
Last update posted
Apr 26, 2016

2008 – 2015

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Mayo Clinic Arizona Scottsdale Arizona 85259
Colorado Blood Cancer Institute Denver Colorado 80218
Moffitt Cancer Center Tampa Florida 33612
Winship Cancer Institute of Emory University Atlanta Georgia 30322
Mass General Hospital Boston Massachusetts 02114
Dana-Farber Cancer Institute Boston Massachusetts 02115
University of Michigan Comprehensive Cancer CenterDivision of Hematology/Oncology Ann Arbor Michigan 48109
Mayo Clinic - Arizona Rochester Minnesota 55905
Washington University School of Medicine St Louis Missouri 63110
The Cancer Center at Hackensack University Medical Center Hackensack New Jersey 07601
Roswell Park Cancer Institute Department of Medicine Buffalo New York 14263
Mt. Sinai Hospital New York New York 10029
Ohio State University Arthur G. James Cancer Hospital Columbus Ohio 43210-1240
University of Pittsburgh Pittsburgh Pennsylvania 15232

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 NCT00833833, 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 Apr 26, 2016 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00833833 live on ClinicalTrials.gov.

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