Drug intelligence / Profile preview

fozivudine tidoxil

Development stage
Phase 2
Lead developer
Heidelberg Pharma
Modality
Small Molecules
Administration
Oral
01

Overview

Fozivudine tidoxil is an investigational small molecule drug developed as a thioether lipid conjugate of zidovudine (AZT), designed to treat HIV infection. It acts as a nucleoside reverse transcriptase inhibitor (NRTI). After oral administration, it is cleaved intracellularly into a lipid moiety and zidovudine-monophosphate, which is then phosphorylated to the active metabolite, zidovudine-triphosphate. This design aims to increase intracellular concentrations of the active drug in mononuclear cells while reducing hematologic toxicity by limiting activation in red blood and stem cells. Fozivudine tidoxil has demonstrated anti-HIV activity in vitro and has undergone Phase II clinical trials for HIV infections[1][2][3][5][6][8].

Other names
fozivudine tidoxilfozivudinefoxivudine tidoxil
02

Targets

Human immunodeficiency virus type 1 reverse transcriptase

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