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
Interventional
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Complete Response Rate to Induction Therapy
10/31/2004
No
United States: Institutional Review Board
HO00401
NCT00581854
June 2000
March 2010
Name | Location |
---|---|
UWCCC | Madison, Wisconsin 53792 |