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Phase II Pilot Study of Hyper-CVAD Plus Rituximab for Previously Untreated Mantle Cell Lymphoma


Phase 2
18 Years
N/A
Not Enrolling
Both
Mantle Cell Lymphoma

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Trial Information

Phase II Pilot Study of Hyper-CVAD Plus Rituximab for Previously Untreated Mantle Cell Lymphoma


rituximab and modified hyperfractionated cyclophosphamide, vincristine doxorubicin,
dexamethasone (hyperCVAD) administered every 28 days for 4-6 cycles followed by rituximab
maintenance therapy consisting of four weekly doses every six months for two years


Inclusion Criteria:



- Untreated mantle cell lymphoma

Exclusion Criteria:

- Pregnant or breast feeding

Type of Study:

Interventional

Study Design:

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Complete Response Rate to Induction Therapy

Outcome Time Frame:

10/31/2004

Safety Issue:

No

Authority:

United States: Institutional Review Board

Study ID:

HO00401

NCT ID:

NCT00581854

Start Date:

June 2000

Completion Date:

March 2010

Related Keywords:

  • Mantle Cell Lymphoma
  • untreated mantle cell lymphoma
  • Lymphoma
  • Lymphoma, Mantle-Cell

Name

Location

UWCCC Madison, Wisconsin  53792