Open-label Study of the Safety and Activity of Oprozomib in Patients With Hematologic Malignancies

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

210

Participants

Timeline

Start Date

October 15, 2011

Primary Completion Date

August 8, 2016

Study Completion Date

August 12, 2019

Conditions
Multiple MyelomaWaldenstrom Macroglobulinemia
Interventions
DRUG

oprozomib

Patients enrolled will receive Oprozomib Tablets once daily either on Days 1-5 (QDx5 schedule) or on Days 1, 2, 8, and 9 (QDx2 weekly schedule) of the 14-day treatment cycle.

Trial Locations (19)

Unknown

Mayo Clinic Scottsdale, Scottsdale

Pacific Cancer Care, Salinas

Colorado Blood Cancer Institute, Denver

Mayo Clinic, Jacksonville

Winship Cancer Institute, Emory University, Atlanta

Rush University Medical Center, Chicago

University of Chicago Medical Center, Chicago

University of Maryland, Greenebaum Cancer Center, Baltimore

Dana Farber Cancer Institute, Boston

Mass General Hospital, Boston

Virginia Piper Cancer Institute, Minneapolis

Mayo Clinic, Rochester

Washington University School of Medicine Division of Oncology, St Louis

John Theurer Cancer Center at Hackensack University, Hackensack

Hematology Oncology of Northern New Jersey, Morristown

New York Oncology Hematology, Albany

Mount Sinai Medical Center, New York

Sarah Cannon Research Institute / Tennessee Oncology, PLLC, Nashville

Columbia Basin Hematology and Oncology, Kennewick

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY

NCT01416428 - Open-label Study of the Safety and Activity of Oprozomib in Patients With Hematologic Malignancies | Biotech Hunter | Biotech Hunter