{"id":913427,"date":"2026-10-02T12:04:11","date_gmt":"2026-10-02T12:04:11","guid":{"rendered":"https:\/\/www.newsbeep.com\/au\/913427\/"},"modified":"2026-10-02T12:04:11","modified_gmt":"2026-10-02T12:04:11","slug":"fda-grants-priority-review-to-high-efficacy-oral-drug-for-2-ms-types","status":"publish","type":"post","link":"https:\/\/www.newsbeep.com\/au\/913427\/","title":{"rendered":"FDA grants priority review to &#8216;high-efficacy&#8217; oral drug for 2 MS types"},"content":{"rendered":"<p>The U.S. Food and Drug Administration (FDA) has agreed to review an application from <a href=\"https:\/\/www.roche.com\/\" rel=\"nofollow noopener\" target=\"_blank\">Roche<\/a> seeking approval of its BTK inhibitor <a href=\"https:\/\/multiplesclerosisnewstoday.com\/fenebrutinib\/\" rel=\"nofollow noopener\" target=\"_blank\">fenebrutinib<\/a> as a treatment for relapsing forms of both <a href=\"https:\/\/multiplesclerosisnewstoday.com\/multiple-sclerosis-overview\/\" rel=\"nofollow noopener\" target=\"_blank\">multiple sclerosis<\/a> (MS) and\u00a0<a href=\"https:\/\/multiplesclerosisnewstoday.com\/primary-progressive-multiple-sclerosis-ppms\/\" rel=\"nofollow noopener\" target=\"_blank\">primary progressive MS<\/a> (PPMS).<\/p>\n<p>Further, the FDA granted the application priority review, under which the regulatory agency aims to make its decision within six months, compared with the 10 months it usually takes. With priority review, a decision on whether or not to approve the treatment candidate \u2014 designed to address two drivers of MS \u2014 would be expected by late March or early April.<\/p>\n<p>Roche said the filing makes fenebrutinib the first BTK inhibitor \u2014 a drug that blocks the abnormal growth of B cells \u2014 to have an application accepted for review for both relapsing forms of MS and PPMS.<\/p>\n<p>\u201cIf approved, fenebrutinib could open a new chapter as the first high-efficacy oral therapy for both relapsing and primary progressive MS, helping to control disease activity while giving people more flexibility and choice,\u201d\u00a0Teresa Graham, CEO of Roche Pharmaceuticals, said in a <a href=\"https:\/\/www.globenewswire.com\/news-release\/2026\/09\/30\/3371506\/0\/en\/roche-s-fenebrutinib-is-the-first-btk-inhibitor-to-receive-u-s-fda-filing-acceptance-in-both-relapsing-and-primary-progressive-multiple-sclerosis.html\" rel=\"nofollow noopener\" target=\"_blank\">company press release<\/a>.<\/p>\n<p>  Recommended Reading<\/p>\n<p>        <img decoding=\"async\" src=\"https:\/\/www.newsbeep.com\/au\/wp-content\/uploads\/2026\/10\/thumbsup_700x350-150x0-c-default.png\" alt=\"Multiple hands are seen giving the thumbs-up sign from inside a black circle.\"\/><\/p>\n<p>MS occurs when the immune system mistakenly launches an inflammatory attack against <a href=\"https:\/\/multiplesclerosisnewstoday.com\/myelin-sheath\/\" rel=\"nofollow noopener\" target=\"_blank\">myelin<\/a>, the protective coating around nerve fibers. In PPMS, symptoms worsen gradually from the onset of the disease, while in relapsing MS, periods of worsening or new symptoms, called relapses, are interspersed by time periods in which symptoms ease.<\/p>\n<p>Fenebrutinib is designed to block a protein called Bruton\u2019s tyrosine kinase (BTK), which is essential for the activity of certain immune cells involved in MS. Inhibiting BTK is expected to reduce the inflammatory attacks that drive <a href=\"https:\/\/multiplesclerosisnewstoday.com\/ms-flares\/\" rel=\"nofollow noopener\" target=\"_blank\">MS relapses<\/a>, as well as the smoldering inflammation inside the brain that contributes to gradual disease progression over time across <a href=\"https:\/\/multiplesclerosisnewstoday.com\/4-types-ms\/\" rel=\"nofollow noopener\" target=\"_blank\">MS types<\/a>.<\/p>\n<p>Roche noted that fenebrutinib aims to ease both \u201cacute inflammation causing relapses and chronic brain inflammation driving disability progression.\u201d<\/p>\n<p>Roche exec says fenebrutinib aims to \u2018go beyond\u2019 relapse control<\/p>\n<p>According to Levi Garraway, MD, PhD, Roche\u2019s chief medical officer, the goal is a new drug that doesn\u2019t just prevent relapses.<\/p>\n<p>\u201cPeople living with multiple sclerosis need treatments that go beyond controlling relapses to help preserve function and independence as the disease progresses,\u201d Garraway said.<\/p>\n<p>The application for fenebrutinib is supported by data from three ongoing Phase 3 clinical studies. In the <a href=\"https:\/\/clinicaltrials.gov\/study\/NCT04586010\" rel=\"nofollow noopener\" target=\"_blank\">FENhance 1 (NCT04586010)<\/a> and <a href=\"https:\/\/clinicaltrials.gov\/study\/NCT04586023\" rel=\"nofollow noopener\" target=\"_blank\">FENhance 2 (NCT04586023)<\/a> twin studies, fenebrutinib treatment for about two years significantly <a href=\"https:\/\/multiplesclerosisnewstoday.com\/news-posts\/2026\/04\/23\/aan-2026-fenebrutinib-outperforms-aubagio-treating-relapsing-ms-trials\/\" rel=\"nofollow noopener\" target=\"_blank\">reduced the average number of relapses<\/a> per year, by more than 50%, compared with <a href=\"https:\/\/multiplesclerosisnewstoday.com\/aubagio-teriflunomide-multiple-sclerosis\/\" rel=\"nofollow noopener\" target=\"_blank\">Aubagio<\/a> (teriflunomide), an approved MS treatment.<\/p>\n<p>In these two studies, which together involve nearly 1,500 adults with relapsing MS, relapse rates equated to about one relapse every 17 years, which Roche said is the lowest ever seen in MS Phase 3 studies.<\/p>\n<p>Fenebrutinib also significantly reduced the number of new and enlarging lesions as well as lesions with active inflammation, by more than 70%, and showed a positive trend toward slower disability progression.<\/p>\n<p class=\"bio-blockquote-text\">Three [late-stage clinical trials] have demonstrated the potential for fenebrutinib to address both relapsing and progressive disease, thereby bringing us closer to an oral treatment that could make a meaningful difference across the MS spectrum.<\/p>\n<p>In the other study, called <a href=\"https:\/\/clinicaltrials.gov\/study\/NCT04544449\" rel=\"nofollow noopener\" target=\"_blank\">FENtrepid (NCT04544449)<\/a>, fenebrutinib was <a href=\"https:\/\/multiplesclerosisnewstoday.com\/actrims\/2026\/02\/09\/actrims-2026-fenebrutinib-matches-ocrevus-ppms-trial\/\" rel=\"nofollow noopener\" target=\"_blank\">shown to be at least as effective<\/a> in adults with PPMS as the approved treatment <a href=\"https:\/\/multiplesclerosisnewstoday.com\/ocrevus-ocrelizumab-primary-progressive-relapsing-multiple-sclerosis\/\" rel=\"nofollow noopener\" target=\"_blank\">Ocrevus<\/a> (ocrelizumab). In fact, while the study was not designed to show significant differences between the drugs, the data demonstrated that fenebrutinib numerically reduced the risk of confirmed disability progression by 12% compared with Ocrevus, the researchers noted.<\/p>\n<p>The scientists noted that a treatment effect was also observed in patients without signs of active inflammation on <a href=\"http:\/\/multiplesclerosisnewstoday.com\/multiple-sclerosis-diagnosis\/mri-magnetic-resonance-imaging\/\" rel=\"nofollow noopener\" target=\"_blank\">MRI scans<\/a>, indicating that fenebrutinib may help slow disability progression even in individuals with less inflammatory activity. This is particularly relevant because patients without signs of active inflammation have been shown to <a href=\"https:\/\/cmsc.confex.com\/cmsc\/2018\/webprogram\/Paper5557.html?utm_source=chatgpt.com\" rel=\"nofollow noopener\" target=\"_blank\">benefit less from Ocrevus<\/a>.<\/p>\n<p>\u201cThree Phase [3] studies have demonstrated the potential for fenebrutinib to address both relapsing and progressive disease, thereby bringing us closer to an oral treatment that could make a meaningful difference across the MS spectrum,\u201d said Garraway, who doubles as head of global product development.<\/p>\n","protected":false},"excerpt":{"rendered":"The U.S. Food and Drug Administration (FDA) has agreed to review an application from Roche seeking approval of&hellip;\n","protected":false},"author":2,"featured_media":913428,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[33],"tags":[64,63,137,490],"class_list":["post-913427","post","type-post","status-publish","format-standard","has-post-thumbnail","category-medication","tag-au","tag-australia","tag-health","tag-medication"],"_links":{"self":[{"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/posts\/913427","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/comments?post=913427"}],"version-history":[{"count":0,"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/posts\/913427\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/media\/913428"}],"wp:attachment":[{"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/media?parent=913427"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/categories?post=913427"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newsbeep.com\/au\/wp-json\/wp\/v2\/tags?post=913427"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}