Drug intelligence / Profile preview

dexamethasone + etoposide + ganciclovir

Development stage
Preclinical
Lead developer
Merck
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

This is a combination regimen consisting of three drugs: - **Dexamethasone** is a synthetic glucocorticoid corticosteroid with potent anti-inflammatory and immunosuppressive properties. It acts primarily by binding to the glucocorticoid receptor, modulating gene expression, and suppressing immune responses. - **Etoposide** is a topoisomerase II inhibitor used as an antineoplastic agent. It induces DNA strand breaks by inhibiting the enzyme topoisomerase II, leading to apoptosis in rapidly dividing cells. - **Ganciclovir** is an antiviral nucleoside analogue that inhibits viral DNA polymerase after phosphorylation, thereby blocking replication of herpesviruses such as cytomegalovirus (CMV). This combination may be used in specific clinical scenarios such as cytomegalovirus-induced haemophagocytic lymphohistiocytosis (HLH) or other severe viral infections with associated immune dysregulation[1]. Each component targets different aspects of disease pathology—dexamethasone for inflammation/immune suppression, etoposide for cytotoxic effects on activated immune cells or malignancy, and ganciclovir for direct antiviral activity against CMV.

02

Targets

GR (Glucocorticoid receptor)TOP2A (DNA topoisomerase II)CMV DNA polymerase (Human cytomegalovirus DNA polymerase)

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