Drug intelligence / Profile preview

favipiravir + nitazoxanide

Development stage
Unknown
Lead developer
FUJIFILM Toyama Chemical
Modality
Small Molecules
Administration
Oral
01

Overview

Favipiravir + nitazoxanide is an investigational oral combination therapy of two small-molecule antivirals with distinct mechanisms of action. Favipiravir is a prodrug that is intracellularly converted to its active form, favipiravir-RTP, which selectively inhibits viral RNA-dependent RNA polymerase (RdRp), thereby blocking viral genome replication and transcription[5][1]. Nitazoxanide acts at a later stage in the viral life cycle by inhibiting maturation of the viral nucleocapsid N protein and thus preventing assembly of new virions[1]. Additionally, nitazoxanide has been shown to modulate host immune responses and inhibit multiple cellular pathways involved in viral entry and replication[4]. The combination has been studied primarily for early treatment of COVID-19 in clinical trials due to their potential additive or synergistic antiviral effects[1][2][3].

Other names
T705T-705T 7052-acetyloxy-N-(5-nitro-2-thiazolyl)benzamide
02

Targets

CTSL (Cathepsin L)HIV-1 proteaseRdRp (Coronavirus RNA-dependent RNA polymerase)

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