Drug intelligence / Profile preview

alemtuzumab + rituximab + mycophenolate mofetil

Development stage
Phase 2
Lead developer
University of Wisconsin–Madison
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

This combination immunosuppressive regimen was developed and evaluated by the University of Wisconsin, Madison, for use in renal transplantation. It consists of induction therapy with alemtuzumab (Campath-1H) and rituximab, followed by maintenance therapy with mycophenolate mofetil (CellCept). The regimen is specifically designed to allow for a calcineurin inhibitor (CNI)-free protocol, aiming to avoid the long-term nephrotoxicity and metabolic side effects (such as hypertension and diabetes) associated with standard CNI-based therapies like tacrolimus or cyclosporine. Alemtuzumab provides potent lymphocyte depletion by targeting CD52, while rituximab targets CD20-positive B cells. Mycophenolate mofetil serves as the primary maintenance agent by inhibiting inosine monophosphate dehydrogenase, thereby suppressing lymphocyte proliferation.

Brand names
Campath + rituximab + CellCeptCampath + rituximab + Myfortic
Other names
UW Madison CNI-free regimen
02

Targets

CD20 (B-lymphocyte antigen CD20)CD52 (CD52 Antigen)IMPDH (Inosine-5'-monophosphate dehydrogenase 1)

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