Phase II Study of Campath-1H Antibody to Treat Waldenstrom's Macroglobulinemia

PHASE2CompletedINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

March 31, 2003

Primary Completion Date

October 31, 2005

Study Completion Date

June 30, 2008

Conditions
Lymphoplasmacytic LymphomaWaldenstrom's Macroglobulinemia
Interventions
DRUG

Campath-1H

Participant will receive three test doses of Campath-1H (3, 10, and 30mg). If this is tolerated then they will receive Campath-IH three times a week for 6 weeks.

Trial Locations (3)

02115

Beth Isreal Deaconness Medical Center, Boston

Dana-farber Cancer Insitiute, Boston

Massachusetts General Hospital, Boston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Brigham and Women's Hospital

OTHER

collaborator

Beth Israel Deaconess Medical Center

OTHER

collaborator

Massachusetts General Hospital

OTHER

collaborator

Bayer

INDUSTRY

collaborator

University of California, Los Angeles

OTHER

collaborator

Northwestern University

OTHER

collaborator

Arizona Oncology Associates

NETWORK

lead

Dana-Farber Cancer Institute

OTHER

NCT00142181 - Phase II Study of Campath-1H Antibody to Treat Waldenstrom's Macroglobulinemia | Biotech Hunter | Biotech Hunter