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Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma Clinical Trials References presented on Clinical Trials Search isn't meant to be a substitute for proven healthcare advice, trips or professional assistance using a genuine physician. We are not docs. Always confer with your physician about Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma conditions. Clinical Trials Search.org is a site devoted to listing clinical research studies in human subjects. Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma Clinical research trials and Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma healthcare trials happen in hundreds of localities throughout the United States of America. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials usually evaluate the potency of new drugs. The propose of the studies / projects is to answer particular human health questions. Clinical trials are a popular way for mDs, government agencies, and private sector companies to detect cures for all sorts of conditions, such as Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma. Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma Clinical Trials and other clinical trials allow volunteers to acquire healthcare treatment choices before they are available to the general public. Some times the subjects recieve professional assistance for free, and every now and again they are compensated for their time. Sometimes there is a cost for a Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma clinical trial. Subjects frequently obtain the most expert healthcare possible for their Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma condition. Risks are a reality, nevertheless, and can include more or frequent doctor trips, medical risks (possibly life-threatening), and/or the treatment being uneffective. Trials are federally governed with stern guidelines to protect clinical trials patients.

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Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma



Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma

For Condition: Melanoma,Neoplasm Metastasis
Status: Completed
Sponsor(s): Celgene Corporation ,
Synopsis: Subjects are randomized to one of two treatment arms. All subjects are screened for eligibility within 28 days prior to randomization. The study consists of a treatment phase and a follow-up phase. Subjects will be treated in repeating 4 week cycles.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: - Understand and voluntarily sign an informed consent form. - Able to adhere to the study visit schedule and other protocol requirements. - Metastatic malignant melanoma now stage IV, relapsed or refractory to standard metastatic therapy. - Women of childbearing potential must have a negative serum or urine pregnancy test within 7 days of starting study drug. - Patients with active brain disease, or newly diagnosed brain metastases, within 4 weeks prior to the start of study treatment are excluded.
Total Enrollment: 274

Location and Contact Information:

MD Anderson Cancer Center
Houston,  Texas,  77030-4009
United States
 

Spectrum Health
Grand Rapids,  Michigan,  49503
United States
 

Cancer Care Manitoba
Winnipeg,  Manitoba,  R3E 0V9
Canada
 

Cross Cancer Institute
Edmonton,  Alberta,  T6G 1Z2
Canada
 

Princess Margaret Hospital
Toronto,  Ontario,  M5G 2M9
Canada
 

Penn State Hershey Medical Center
Hershey,  Pennsylvania,  17033-0850
United States
 

Massachusetts General Hospital
Boston,  Massachusetts,  02214-2698
United States
 

Lutheran General
Park Ridge,  Illinois,  60068-1270
United States
 

Washington University School of Medicine
St. Louis,  Missouri,  63110
United States
 

Carle Clinic
Urbana,  Illinois,  61801
United States
 

University of Colorado
Aurora,  Colorado,  80010
United States
 

The Linder Clinical Trial Center
Cincinnati,  Ohio,  45219
United States
 

Biomedical Research Alliance of New York
New York City,  New York,  10016
United States
 

Beth Israel Deaconess Medical Ctr
Boston,  Massachusetts,  02215-5400
United States
 

Outpatient Clinic
Santa Monica,  California,  90404
United States
 

UPMC Cancer Pavillion
Pittsburgh,  Pennsylvania,  15232
United States
 

Sarah Cannon Cancer Center
Nashville,  Tennessee,  37203-1632
United States
 

Lakeland Regional Cancer Center
Lakeland,  Florida,  33804-1057
United States
 

Qell Health Sciences Center
Halifax,  Nova Scotia,  B3H 2y9
Canada
 

Cleveland Clinic Foundation
Cleveland,  Ohio,  44195
United States
 

University of Southern California Norris Cancer Center
Los Angeles,  California,  90089
United States
 

UCLA
Los Angeles,  California,  90095-6956
United States
 

Mount Sinai Comprehensive Cancer Center
Miami,  Florida,  33140
United States
 

Melanoma Center of St Louis
St. Louis,  Missouri,  63131
United States
 

Memorial Sloan Kettering Cancer Center
New York City,  New York,  10021
United States
 

The Harold Lever Regional Cancer Center
Waterbury,  Connecticut,  06708
United States
 

L'Hotel Dieu de Quebec
Quebec,  ,  PQ G1R 2J6
Canada
 

University of Arizona Cancer Center
Tucson,  Arizona,  85724
United States
 

Ellis Fischel Cancer Center
Columbia,  Missouri,  65203
United States
 

St. Francis Memorial Hospital
San Francisco,  California,  94109
United States
 

Tom Baker Cancer Center
Calgary,  Alberta,  T2N 4N2
Canada
 


Additional Information:
Study ID Numbers:
  CDC-5013-MEL-001; 
Study Start Date: January 2003
Record last reviewed: May 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00055562

Other Melanoma Studies:
1. Immunization of HLA-A201 Patients with Metastatic Melanoma Using a Combination of Immunodominant Peptides from Three Melanoma Antigens, MART-1, GP100 and Tyrosinase

2. Treatment of Patients with Cancer with Genetically Modified Salmonella Typhimurium Bacteria

3. Liver Perfusion of Melphalan in Inoperable Liver Cancer

4. Treatment of Patients with Metastatic Melanoma Using Cloned Peripheral Blood Lymphocytes Sensitized In Vitro to the gp209-2M Immunodominant Peptide

5. A Phase I/II Trial of Vaccination with Mutant Ras Peptide Pulsed Dendritic Cells in the Treatment of HLA A2.1 Positive Patients with Colorectal Cancer

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Study to Compare the Efficacy and Safety of Two CC-5013 Dose Regimens in Subjects with Metastatic Malignant Melanoma

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