Study to Evaluate the Efficacy and Safety of CUDC-907 in Patients With RR DLBCL, Including Patients With MYC Alterations

PHASE2CompletedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

July 31, 2016

Primary Completion Date

May 28, 2019

Study Completion Date

May 28, 2019

Conditions
Relapsed and/or Refractory Diffuse Large B-cell Lymphoma Including With Myc Alterations
Interventions
DRUG

CUDC-907

Trial Locations (25)

17033

Penn State Hershey Cancer Institute-Clinical Trials Office, Hershey

19104

Hospital of the University of Pennsylvania, Philadelphia

19111

Fox Chase Cancer Center, Philadelphia

28220

Hospital Universitario Puerta de Hierro, Madrid

30322

Winship Cancer Institute of Emory University, Atlanta

33612

Moffitt Cancer Center, Tampa

37007

Hospital Universitario de Salamanca, Salamanca

37203

Tennessee Oncology Sarah Cannon, Nashville

37920

University of Tennessee Cancer Center, Knoxville

40207

Norton Cancer Institute, Louisville

48201

Karmanos Cancer Institute, Detroit

55905

Mayo Clinic, Rochester

University of Rochester, Rochester

60647

University of Chicago, Chicago

73104

University of Oklahoma Health Sciences Center (OUHSC), Oklahoma City

74104

Cancer Care Associates, Tulsa

75246

Charles A. Sammons Cancer Center, Dallas

77030

Houston Methodist Hospital, Houston

The University of Texas M.D. Anderson Cancer Center, Houston

90033

University of Southern California, Norris Comprehensive Cancer Center, Los Angeles

93701

University of California San Francisco-Fresno, Fresno

98104

Swedish Cancer Institute, Seattle

08035

Hospital Universitari Vall d'Hebron, Barcelona

08041

Hospital de la Santa Creu i Sant Pau, Barcelona

08908

Hospital Durán i Reynals, Servicio de Oncología, Barcelona

All Listed Sponsors
lead

Curis, Inc.

INDUSTRY

NCT02674750 - Study to Evaluate the Efficacy and Safety of CUDC-907 in Patients With RR DLBCL, Including Patients With MYC Alterations | Biotech Hunter | Biotech Hunter