<p>Regeneron Pharmaceuticals said on Tuesday initial data from an ongoing study of its experimental antibody cocktail for use in some hospitalized Covid-19 patients show the therapy was sufficiently effective to warrant continuing the trial.</p>.<p>The company is testing the therapy, a combination of two antibodies casirivimab and imdevimab, in hospitalized patients requiring low-flow oxygen.</p>.<p>The drugmaker said in September the cocktail reduced viral levels and improved symptoms in non-hospitalized Covid-19 patients.</p>.<p>Study participants included those who produced an effective immune response on their own (seropositive), and those whose immune response was not yet adequate (seronegative).</p>.<p>Seronegative patients treated with the antibody cocktail had a lower risk of death or needing mechanical ventilation, the company said.</p>.<p>Based on these results, the company said an ongoing late-stage study in hospitalized patients will continue.</p>.<p>The US Food and Drug Administration last month issued emergency use authorization for the antibody therapy for use in mild to moderate Covid-19 patients who are not currently hospitalized.</p>
<p>Regeneron Pharmaceuticals said on Tuesday initial data from an ongoing study of its experimental antibody cocktail for use in some hospitalized Covid-19 patients show the therapy was sufficiently effective to warrant continuing the trial.</p>.<p>The company is testing the therapy, a combination of two antibodies casirivimab and imdevimab, in hospitalized patients requiring low-flow oxygen.</p>.<p>The drugmaker said in September the cocktail reduced viral levels and improved symptoms in non-hospitalized Covid-19 patients.</p>.<p>Study participants included those who produced an effective immune response on their own (seropositive), and those whose immune response was not yet adequate (seronegative).</p>.<p>Seronegative patients treated with the antibody cocktail had a lower risk of death or needing mechanical ventilation, the company said.</p>.<p>Based on these results, the company said an ongoing late-stage study in hospitalized patients will continue.</p>.<p>The US Food and Drug Administration last month issued emergency use authorization for the antibody therapy for use in mild to moderate Covid-19 patients who are not currently hospitalized.</p>