Combination Bortezomib and Rituximab in Patients With Waldenstrom's Macroglobulinemia (WM)

Part of paid clinical trials in Boston, Massachusetts.

Sponsor
Dana-Farber Cancer Institute
Study ID
NCT00422799
Phase
PHASE2
Status
Completed

Conditions

  • Waldenstrom's Macroglobulinemia

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Bortezomib — DRUG
    Once weekly for 3 weeks
  • Rituximab — DRUG
    Intravenously once a week for the first and fourth weeks of a cycle

Study Details

In this study, we are trying to find out if the combination of these two drugs is effective in treating Waldenstrom's macroglobulinemia (WM). The combination of these two drugs has not been studied for patients with relapsed or refractory macroglobulinemia. The U.S. Food and Drug Administration (FDA) has approved bortezomib for the treatment of multiple myeloma, a cancer that is closely related to Waldenstrom's macroglobulinemia.

Key Dates

Start date
Aug 30, 2006
Status verified
Oct 2020
Primary completion
Oct 9, 2015
Completion
Oct 9, 2015

Study Design

Enrollment
63 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: bortezomib and rituximab
    bortezomib and rituximab

Primary Outcome Measure

Overall Response Rate of Bortezomib and Rituximab (VR) in Patients With Relapsed or Refractory Waldenstrom's Macroglobulinemia (WM) [ Time Frame: 2 Years ]

Locations (1)

FacilityCityStateZIPSite coordinators
Dana-Farber Cancer InstituteBostonMassachusetts02115-

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