Study to Investigate the Safety and Tolerability of Odronextamab in Patients With CD20+ B-Cell Malignancies

PHASE1CompletedINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

January 9, 2015

Primary Completion Date

August 21, 2025

Study Completion Date

August 21, 2025

Conditions
Non-Hodgkin LymphomaChronic Lymphocytic Leukemia
Interventions
DRUG

Odronextamab multiple dose levels

Administered by intravenous (IV) infusion

DRUG

Odronextamab multiple dose levels

Administered by subcutaneous (SC) injection

Trial Locations (22)

10065

Memorial Sloan Kettering Cancer Center, New York

Weill Cornell Medical College, New York

33612

H. Lee Moffitt Cancer Center, Tampa

44281

Meir Medical Center, Kfar Saba

55905

Mayo Clinic, Rochester

69495

CHU Hôpital Lyon Sud, Lyon

76038

Centre Henri Becquerel, Rouen

92868

University of California, Irvine, Orange

94305

Stanford University, Stanford

94800

Institut Gustave Roussy, Villejuif

97080

Universitatsklinikum Wurzburg, Würzburg

3109601

Rambam Health Care Campus - Hematology and Bone Marrow Transplantation Institute, Haifa

3436212

Lady Davis Carmel Medical Center, Haifa

5265601

The Chaim Sheba Medical Center, Tel-Hashomer

7747629

Assuta Ashdod University Hospital, Ashdod

9112001

Hadassah Medical Center, Jerusalem

02114

Massachusetts General Hospital, Boston

02215

Beth Israel Deaconess Medical Center, Boston

Dana Farber Cancer Institute (Massachusetts General Hospital and Beth Israel), Boston

08901

Rutgers Cancer Institute of New Jersey, New Brunswick

tr1 3lq

Royal Cornwall Hospitals NHS Trust, Truro

M20 4BX

The Christie NHS Foundation Trust, Manchester

All Listed Sponsors
lead

Regeneron Pharmaceuticals

INDUSTRY

NCT02290951 - Study to Investigate the Safety and Tolerability of Odronextamab in Patients With CD20+ B-Cell Malignancies | Biotech Hunter | Biotech Hunter