{"id":12082,"date":"2021-06-07T14:24:00","date_gmt":"2021-06-07T17:24:00","guid":{"rendered":"https:\/\/portaldasaudenews.com\/?p=12082"},"modified":"2021-06-07T14:24:00","modified_gmt":"2021-06-07T17:24:00","slug":"agencia-reguladora-americana-aprova-medicamento-para-alzheimer","status":"publish","type":"post","link":"https:\/\/portaldasaudenews.com\/?p=12082","title":{"rendered":"Ag\u00eancia reguladora americana aprova medicamento para Alzheimer"},"content":{"rendered":"<p>&nbsp;<\/p>\n<p><span style=\"font-weight: 400;\">Os reguladores dos EUA aprovaram nesta segunda-feira(7) o aducanumabe da Biogen Inc (BIIB.O) como o primeiro tratamento para a\u00a0 causa prov\u00e1vel da doen\u00e7a de Alzheimer, apesar da controv\u00e9rsia sobre se a evid\u00eancia cl\u00ednica prova que a droga funciona.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O aducanumabe visa remover dep\u00f3sitos pegajosos de uma prote\u00edna chamada beta amil\u00f3ide do c\u00e9rebro de pacientes em est\u00e1gios iniciais de Alzheimer, a fim de evitar sua devasta\u00e7\u00e3o, que inclui perda de mem\u00f3ria e incapacidade de cuidar de si mesmo.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O especialista em doen\u00e7a de Alzheimer na Mayo ClinicDr. Ronald Petersen, disse \u00e0 Ag\u00eancia Reuters que &#8220;esta \u00e9 uma boa not\u00edcia para os pacientes com doen\u00e7a de Alzheimer. Nunca tivemos uma terapia modificadora da doen\u00e7a aprovada&#8221;. Isso n\u00e3o \u00e9 uma cura. Espera-se que isso diminua a progress\u00e3o da doen\u00e7a\u201d, advertiu.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">&#8220;Acho que este \u00e9 um grande dia&#8221;, disse Peterson. &#8220;Mas n\u00e3o podemos prometer demais.&#8221;<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A Food and Drug Administration disse em seu site que os ensaios cl\u00ednicos para o tratamento, a ser vendido sob a marca Aduhelm, mostraram uma redu\u00e7\u00e3o nas placas que deve levar a um decl\u00ednio mais lento nos pacientes.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">&#8220;Embora os dados do Aduhelm sejam complicados com rela\u00e7\u00e3o aos seus benef\u00edcios cl\u00ednicos, o FDA determinou que h\u00e1 evid\u00eancias substanciais de que o Aduhelm reduz as placas de beta amil\u00f3ide no c\u00e9rebro e que a redu\u00e7\u00e3o nessas placas \u00e9 razoavelmente prov\u00e1vel de prever benef\u00edcios importantes para os pacientes&#8221; ag\u00eancia disse em um comunicado.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Ainda segundo a Reuters, o medicamento da Biogen foi aclamado por defensores dos pacientes e alguns neurologistas ansiosos por ter uma op\u00e7\u00e3o eficaz para pacientes com a doen\u00e7a letal. Outros m\u00e9dicos disseram que os resultados dos testes cl\u00ednicos eram inconsistentes e que mais provas eram necess\u00e1rias.<\/span><\/p>\n<h2><span style=\"color: #008000;\"><strong>Pre\u00e7o<\/strong><\/span><\/h2>\n<p><span style=\"font-weight: 400;\">O Institute for Clinical and Economic Review, um influente grupo de pesquisa de pre\u00e7os de medicamentos, em um relat\u00f3rio de maio citou evid\u00eancias &#8220;insuficientes&#8221; de que o aducanumabe fornece um benef\u00edcio l\u00edquido \u00e0 sa\u00fade. Ele disse que os dados at\u00e9 agora indicam um pre\u00e7o econ\u00f4mico de n\u00e3o mais do que US $ 8.300 por ano. Olhando apenas para resultados de ensaios favor\u00e1veis, o pre\u00e7o sobe para US $ 23.100, disse o ICER<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O grupo de pesquisa definiu o pre\u00e7o justo para qualquer medicamento comprovadamente capaz de interromper a progress\u00e3o da dem\u00eancia relacionada ao Alzheimer em US $ 50.000 a US $ 70.000 por ano.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">&#8220;Achamos que a droga tem potencial para gerar (pelo menos) US $ 10 bilh\u00f5es em vendas de pico e acreditamos que um lan\u00e7amento bem-sucedido de aducanumabe tem o potencial de mudar completamente o perfil da empresa&#8221;, disse o analista do Guggenheim Yatin Suneja.<\/span><\/p>\n<h2><span style=\"color: #008000;\"><strong>Tratamento<\/strong><\/span><\/h2>\n<p><span style=\"font-weight: 400;\">Os tratamentos atuais de Alzheimer, incluindo o Namenda da AbbVie (ABBV.N) e o Aricept da Pfizer (PFE.N), destinam-se a aliviar os sintomas da doen\u00e7a de Alzheimer, enquanto a droga Biogen \u00e9 a primeira aprovada para atacar a causa subjacente da dem\u00eancia e progress\u00e3o lenta.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O FDA disse que a Biogen precisar\u00e1 conduzir um teste p\u00f3s-aprova\u00e7\u00e3o para verificar o benef\u00edcio cl\u00ednico do Aduhelm, e que ele pode ser retirado do mercado se o medicamento n\u00e3o funcionar conforme o esperado.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">&#8220;Acho que eles tomaram a decis\u00e3o certa. Torna o medicamento dispon\u00edvel para os pacientes enquanto exige que a empresa fa\u00e7a mais pesquisas para provar seus benef\u00edcios. Acho que todos ganham&#8221;, disse o Dr. Howard Fillit, diretor de ci\u00eancias da a Alzheimer&#8217;s Drug Discovery Foundation.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O aducanumabe foi estudado em pacientes com doen\u00e7a inicial com teste positivo para um componente das placas cerebrais amil\u00f3ides.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Alguns pacientes experimentados experimentaram um incha\u00e7o cerebral potencialmente perigoso. O FDA aconselhou que os pacientes que apresentarem o efeito colateral devam ser monitorados, mas n\u00e3o necessariamente retirados do medicamento.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A decis\u00e3o da FDA n\u00e3o definiu os pacientes de Alzheimer espec\u00edficos para os quais o tratamento \u00e9 apropriado &#8211; como a doen\u00e7a em est\u00e1gio inicial &#8211; levantando a possibilidade de que a popula\u00e7\u00e3o de pacientes seja maior do que o previsto. O FDA n\u00e3o estava imediatamente dispon\u00edvel para comentar.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A Biogen estimou que cerca de 1,5 milh\u00e3o de americanos seriam eleg\u00edveis para o tratamento com aducanumabe, que \u00e9 administrado por infus\u00e3o mensal, levantando preocupa\u00e7\u00f5es sobre os custos para o sistema de sa\u00fade.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O n\u00famero de americanos que vivem com Alzheimer considerada a sexta causa de morte nos Estados Unidos. deve aumentar para cerca de 13 milh\u00f5es em 2050, de mais de 6 milh\u00f5es atualmente, de acordo com a Associa\u00e7\u00e3o de Alzheimer.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A teoria da amiloide tem estado no centro da pesquisa de Alzheimer por muitos anos, com uma longa lista de falhas para mostrar para ela, e parecia em suporte de vida at\u00e9 que a Biogen reviveu seu programa de aducanumabe.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p>*Com informa\u00e7\u00f5es da Reuters<\/p>\n<p>*Foto: Scott Eisen\/Bloomberg<\/p>\n","protected":false},"excerpt":{"rendered":"<p>&nbsp; Os reguladores dos EUA aprovaram nesta segunda-feira(7) o aducanumabe da Biogen Inc (BIIB.O) como<\/p>\n","protected":false},"author":1,"featured_media":3248,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[16,31],"tags":[],"class_list":["post-12082","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-mundo","category-saude-mundo"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - 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