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Spots Global Cancer Trial Database for A Study of Tanespimycin (KOS-953) in Patients With Multiple Myeloma in First Relapse

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Trial Identification

Brief Title: A Study of Tanespimycin (KOS-953) in Patients With Multiple Myeloma in First Relapse

Official Title: Phase 3 Randomized, Open-Label Clinical Trial of Tanespimycin (KOS-953) Plus Bortezomib Compared to Bortezomib Alone in Patients With Multiple Myeloma in First Relapse

Study ID: NCT00546780

Study Description

Brief Summary: This is a phase 3, open label trial for patients with multiple myeloma in first relapse. Trial will compare tanespimycin (KOS-953), in combination with a fixed dose of bortezomib versus bortezomib alone.

Detailed Description: Phase 3 combination study comparing tanespimycin (KOS-953) plus bortezomib to bortezomib alone in patients with multiple myeloma in first relapse after failure of previous anti-cancer therapy and/or bone marrow transplantation. Primary objective is to compare the progression-free survival (PFS) associated with the use of tanespimycin (KOS-953) in combination with bortezomib versus that associated with administration of bortezomib alone.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Comprehensive Blood And Cancer Center, Bakersfield, California, United States

Moores Ucsd Cancer Center, La Jolla, California, United States

University Of California Medical Center, San Francisco, California, United States

Rocky Mountain Cancer Centers, Denver, Colorado, United States

University Of Iowa Hospitals And Clinics, Iowa City, Iowa, United States

University Of Kansas Medical Center, Westwood, Kansas, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Henry Ford Health System Irb, Detroit, Michigan, United States

Capitol Comprehensive Cancer Care Center, Jefferson City, Missouri, United States

Columbia University Medical Center (Cumc), New York, New York, United States

Wake Forest Univ Health Sciences, Winston-Salem, North Carolina, United States

Kaiser Permanente Oncology/Hematology, Portland, Oregon, United States

Thomas Jefferson University, Philadelphia, Pennsylvania, United States

Tennessee Cancer Specialists, Knoxville, Tennessee, United States

Sarah Cannon Research Institute, Nashville, Tennessee, United States

Baylor University Medical Center, Dallas, Texas, United States

University Of Virginia Health System, Charlottesville, Virginia, United States

Medical College Of Wisconsin, Milwaukee, Wisconsin, United States

Local Institution, Edmonton, Alberta, Canada

Contact Details

Name: Bristol-Myers Squibb

Affiliation: Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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