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Early Treatment with Pegylated Interferon Lambda for Covid-19

Authors:
Gilmar Reis, Eduardo A.S. Moreira Silva, Daniela C. Medeiros Silva, Lehana Thabane, Vitoria H.S. Campos, Thiago S. Ferreira, Castilho V.Q. Santos, Ana M.R. Nogueira, Ana P.F.G. Almeida, Leonardo C.M. Savassi, Adhemar D. Figueiredo-Neto et al.

Abstract

This phase 3, randomized, placebo-controlled trial evaluates the efficacy of a single dose of pegylated interferon lambda for treating outpatients with symptomatic Covid-19. Conducted in Brazil and Canada, the trial enrolled predominantly vaccinated adults within 7 days of symptom onset. The treatment group had significantly fewer Covid-19-related hospitalizations and extended emergency department visits than the placebo group (2.7% vs. 5.6%), with a relative risk reduction of 51%. Benefits were consistent across variants, vaccination statuses, and patients with high baseline viral loads. The study supports interferon lambda as a potentially convenient antiviral option with broad-spectrum efficacy and an acceptable safety profile.

Keywords: pegylated interferon lambda Covid-19 SARS-CoV-2 adaptive platform trial outpatient treatment antiviral therapy vaccination status hospitalization reduction viral load phase 3 trial
DOI: https://doi.ms/10.00420/ms/9075/S1HFN/XTP | Volume: 388 | Issue: 6 | Views: 0
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