Drug intelligence / Profile preview

prednisolone + mycophenolate mofetil

Development stage
Unknown
Lead developer
Roche
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, Irreversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules
Administration
Oral, Intravenous
01

Overview

This is a combination therapy consisting of prednisolone, a synthetic glucocorticoid corticosteroid, and mycophenolate mofetil, an immunosuppressive antimetabolite. Prednisolone acts primarily by binding to the glucocorticoid receptor and modulating gene expression to suppress inflammation and immune responses. Mycophenolate mofetil is a prodrug that is rapidly converted to mycophenolic acid, which selectively inhibits inosine monophosphate dehydrogenase (IMPDH), blocking de novo purine synthesis in lymphocytes and thereby inhibiting T- and B-cell proliferation. This combination has been used for various autoimmune diseases (such as lupus nephritis, idiopathic thrombocytopenic purpura [ITP], retroperitoneal fibrosis) as well as in organ transplantation settings to prevent rejection[1][2][3][4][5][7][10]. The regimen leverages the anti-inflammatory effects of prednisolone with the potent immunosuppressive action of mycophenolate mofetil.

Other names
prednisolone and mycophenolate mofetilMMF and prednisolonemycophenolate mofetil and corticosteroid
02

Targets

GR (Glucocorticoid receptor)IMPDH (Inosine-5'-monophosphate dehydrogenase 1)

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