Anvisa autoriza Biomm a realizar estudo de fase 3 de medicamento contra covid-19
A farmacêutica Biomm informou ter recebido, da Agência Nacional de Vigilância Sanitária (Anvisa), autorização para iniciar os estudos clínicos de fase 3 do medicamento leronlimab, em aplicação contra a covid-19, no Brasil.
A pesquisa será realizada em 35 centros e envolverá 612 pacientes diagnosticados com covid-19 que se encontram hospitalizados e com necessidade de suporte para oxigenação. O objetivo do remédio é impedir que a doença evolua para um quadro mais grave, com necessidade de ventilação mecânica invasiva.
O leronlimab é um medicamento biológico e age para prevenir uma resposta excessiva do sistema imunológico de pacientes infectados com o novo coronavírus, reduzindo a superprodução de citocinas inflamatórias, também conhecidas como “tempestade de citocinas”.
Segundo a farmacêutica, esta tempestade inflamatória, que agrava a condição clínica...
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