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Europe may approve Roche’s Gazyva for severe lupus nephritis, showing better kidney results and less steroid use in trials.
The European Medicines Agency's CHMP has recommended approval of Roche’s Gazyva/Gazyvaro combined with mycophenolate mofetil for treating adult patients with severe lupus nephritis, based on phase III trial results showing improved kidney response and reduced steroid use.
The drug, which targets B cells, demonstrated better outcomes than standard therapy alone.
A final decision by the European Commission is pending, while the U.S. FDA is expected to rule on a similar application this year.
Lupus nephritis affects over 1.7 million people globally, primarily women of color, and can lead to kidney failure.
There is currently no cure.
Europa puede aprobar Gazyva de Roche para la nefritis lúpica grave, mostrando mejores resultados renales y menos uso de esteroides en ensayos.