Favipiravir PEP shows non-significant reduction in SARS-CoV-2 infection among household contacts in Thailand trial
This phase 2/3 cluster-randomized controlled trial evaluated favipiravir post-exposure prophylaxis (FPV-PEP) for preventing SARS-CoV-2 infection among household contacts in Thailand. The study included 168 close contacts from 76 index cases, comparing FPV-PEP (1600-2000 mg/day for 7 days) against usual care. The primary outcome was incidence of confirmed SARS-CoV-2 infection.
Results showed a lower incidence of infection in the FPV-PEP group (7.32%) compared to usual care (14.47%), though this difference did not reach statistical significance. Secondary outcomes suggested less frequent symptom development (fever, rhinorrhea, myalgia), a higher probability of remaining asymptomatic, and delayed symptom onset among FPV-PEP recipients, though exact numbers for these outcomes were not reported.
No participants developed severe COVID-19 or required hospitalization. The study had several limitations: it was open-label, the primary outcome difference was not statistically significant, and it was a phase 2/3 trial. Key details including follow-up duration, adverse events, and funding sources were not reported.
For clinical practice, these findings represent early evidence that requires confirmation. The observed association between FPV-PEP and reduced infection/symptoms should be interpreted cautiously given the non-significant primary outcome and open-label design.