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ProLectin-M, an oral antiviral, showed rapid viral clearance and clinical improvement in hospitalized COVID-19 patients during a small Indian trial.
Bioxytran, Inc. announced positive Phase 1b/2a trial results for its oral antiviral ProLectin-M in hospitalized patients with mild to moderate COVID-19.
In a study of 39 participants in India, the highest dose (16,800 mg/day) led to significantly earlier viral clearance by Day 5, with 90% of patients showing no detectable virus versus 20% in the placebo group (p=0.001).
A 2-point improvement on the WHO Ordinal Scale was seen in 90% of high-dose patients by Day 5.
All participants improved clinically by Day 7.
ProLectin-M was well tolerated with no serious adverse events.
The drug targets galectins, host proteins viruses use to enter cells, suggesting potential against multiple viruses.
Bioxytran plans larger trials and is pursuing U.S. and international regulatory review.
ProLectin-M, un antiviral oral, mostró una rápida eliminación viral y una mejora clínica en pacientes hospitalizados con COVID-19 durante un pequeño ensayo en la India.