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The FDA grants Breakthrough Therapy status to a new MS drug showing significant benefits.
The FDA has granted Breakthrough Therapy designation to tolebrutinib for treating adults with non-relapsing secondary progressive multiple sclerosis (SPMS).
This designation follows positive results from a phase 3 study showing the drug delayed disability progression by 31% compared to a placebo.
It aims to expedite the drug's development and review, given its potential to significantly improve treatment for serious medical conditions.
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La FDA otorga el estatus de Terapia Breakthrough a un nuevo medicamento de MS que muestra beneficios significativos.