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A Agência Nacional de Vigilância Sanitária (Anvisa) aprovou o registro de cinco novos medicamentos à base de semaglutida, princípio ativo utilizado no tratamento do diabetes e da obesidade. A decisão ocorre após o Ministério da Saúde solicitar, em agosto de 2025, prioridade na análise desses produtos, com o objetivo de ampliar o acesso da população a essa tecnologia,reduzir a dependência de importações, estimular a concorrência e contribuir para a redução dos preços no mercado brasileiro.
- Owozy (Ávita Care)
- Seemasun (Sun Farmacêutica)
- Zempneo (Brainfarma)
- Semavy (Cosmed)
- Orsema (Ranbaxy)
Paralelamente, o Ministério da Saúde acompanha um estudo com medicamentos da classe GLP-1 no Grupo Hospitalar Conceição (GHC), em Porto Alegre. A pesquisa envolve cerca de 250 pacientes com obesidade grave e os primeiros resultados são esperados para 2027, podendo contribuir para futuras decisões sobre a oferta desses tratamentos no SUS.
Atualmente, os medicamentos da classe GLP-1 ainda não são disponibilizados pelo Sistema Único de Saúde (SUS), mas a incorporação da semaglutida está em análise pela Conitec.
Além de ampliar as opções terapêuticas disponíveis no mercado, a aprovação dos novos registros fortalece a indústria farmacêutica nacional. Entre os medicamentos à base de semaglutida já aprovados pela Anvisa, dois são produzidos no Brasil pelas empresas EMS e Germed Farmacêutica.