Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Favipiravir HU is a specific oral formulation of the antiviral agent favipiravir, developed and evaluated by the University of Pecs in Hungary for the treatment of SARS-CoV-2 infection. As a prodrug, favipiravir is ribosylated and phosphorylated intracellularly to form its active metabolite, favipiravir-ribofuranosyl-5'-triphosphate (favipiravir-RTP). This active form acts as a potent and selective inhibitor of the viral RNA-dependent RNA polymerase (RdRp). By mimicking purine nucleotides, it is incorporated into the viral RNA strand, leading to chain termination or lethal mutagenesis, thereby halting viral replication. The University of Pecs initiated a Phase 2 clinical trial to assess the safety and efficacy of this formulation as an add-on therapy to standard of care in patients with asymptomatic to mild COVID-19, specifically noting that the study was intended for pandemic response rather than formal regulatory registration.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Favipiravir HU.