Safety and Efficacy Study of Catumaxomab to Treat Ovarian Cancer After a Complete Response to Chemotherapy

PHASE2CompletedINTERVENTIONAL
Enrollment

47

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

February 29, 2008

Study Completion Date

February 29, 2008

Conditions
Ovarian Cancer
Interventions
DRUG

catumaxomab

Catumaxomab administered as four 3-hour, constant-rate, intraperitoneal (IP) infusions of 10, 20, 50, 150 microgram (mcg).

Trial Locations (12)

15213

Magee-Women Hospital of UPMC, Pittsburgh

27157

Wake Forest University Health Sciences, Winston-Salem

29210

South Carolina Oncology Associates, Columbia

32804

Florida Hospital Cancer Institute, Orlando

40202

James Graham Brown Cancer Center, Louisville

46617

Michiana Hematology Oncology P.C., South Bend

60521

Gynecologic Oncology - Hinsdale, Hinsdale

85724

Arizona Cancer Center, Tucson

87131

University of New Mexico, Albuquerque

94305

Stanford University of Obstetrics and Gynecology, Stanford

02114

Massachusetts General Hospital, Boston

03756

Dartmouth-Hitchcock Medical Center, Lebanon

Sponsors
All Listed Sponsors
collaborator

Fresenius Biotech North America

INDUSTRY

lead

Neovii Biotech

INDUSTRY