{"id":128150,"date":"2025-09-02T21:37:14","date_gmt":"2025-09-02T21:37:14","guid":{"rendered":"https:\/\/www.newsbeep.com\/us\/128150\/"},"modified":"2025-09-02T21:37:14","modified_gmt":"2025-09-02T21:37:14","slug":"rankin-county-family-meets-with-fda-commissioner-over-rare-disease-medication-denial","status":"publish","type":"post","link":"https:\/\/www.newsbeep.com\/us\/128150\/","title":{"rendered":"Rankin County family meets with FDA Commissioner over rare disease medication denial"},"content":{"rendered":"<p class=\"text | article-text\">RICHLAND, Miss. (WLBT) &#8211; A Rankin County family\u2019s fight to get a drug approved takes them to Washington, D.C., where they had a sit-down with the FDA Commissioner.<\/p>\n<p class=\"text | article-text\">After a peaceful demonstration with other families impacted by Barth Syndrome, they have hope for future access to a medication denied by the agency.<\/p>\n<p class=\"text | article-text\">\u201cWe were there on a wing and a prayer, and we got it,\u201d said Kristi Pena.<\/p>\n<p class=\"text | article-text\">The 44-year-old and her sister, Amy Wilson, both having sons with Barth Syndrome, traveled to the nation\u2019s capital to the Food and Drug Administration to approve the drug Elamipretide.<\/p>\n<p class=\"text | article-text\">They hoped to meet FDA Commissioner Dr. Martin Makary, but it was a long shot.<\/p>\n<p class=\"text | article-text\">\u201cOut of 75 letters written requesting a face-to-face meeting, my letter was chosen for a face-to-face,\u201d said Pena.<\/p>\n<p class=\"text | article-text\">They were joined by five other Barth Syndrome families and the organization\u2019s executive director, sharing their experiences and Elamipretide data with Makary.<\/p>\n<p class=\"text | article-text\">\u201cIt was an empowering experience,\u201d said Pena. \u201cWe felt out of nine years of this battle with the FDA, finally we felt heard. We feel hopeful that there will be an answer.\u201d<\/p>\n<p class=\"text | article-text\">The women learned that the FDA will decide on the drug by September 26.<\/p>\n<p class=\"text | article-text\">Elamipretide, which was previously discontinued, will now be available through the end of September.<\/p>\n<p class=\"text | article-text\">In August, the manufacturer, Stealth Bio Therapeutics, announced that their doors would be closed and there would be no access to the medication after the end of August.<\/p>\n<p class=\"text | article-text\">\u201cOnce we got to D.C., we had a meeting with the Barth Syndrome Foundation that told us that the drug manufacturer had indeed filed another drug application, [and] that they had 30 days to accept that application. They [the FDA] did so in less than a week, which was very encouraging for us,\u201d said Amy Wilson. <\/p>\n<p class=\"text | article-text\">After six days in D.C., they are optimistic the life-changing drug will get approved this third time, but said it needs to be extended to children two to 12 years old.<\/p>\n<p class=\"text | article-text\">\u201cHopefully, a good resolution because we\u2019re not gonna stop until this medication is approved for all ages,\u201d added Pena.<\/p>\n<p class=\"text | article-text\">Want more WLBT news in your inbox? <a href=\"https:\/\/www.wlbt.com\/newsletter\/\" rel=\"nofollow noopener\" target=\"_blank\">Click here<\/a> to subscribe to our newsletter.<\/p>\n<p class=\"text | article-text\">See a spelling or grammar error in our story? Please <a href=\"https:\/\/www.wlbt.com\/2025\/09\/01\/rankin-county-family-meets-with-fda-commissioner-over-rare-disease-medication-denial\/mailto:wlbt-digitalcontent@gray.tv\" target=\"_blank\" title=\"\" rel=\"nofollow noopener\">click here<\/a> to report it and include the headline of the story in your email.<\/p>\n<p class=\"copyright |\">Copyright 2025 WLBT. All rights reserved.<\/p>\n","protected":false},"excerpt":{"rendered":"RICHLAND, Miss. (WLBT) &#8211; A Rankin County family\u2019s fight to get a drug approved takes them to Washington,&hellip;\n","protected":false},"author":2,"featured_media":64325,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[58],"tags":[4,2408,97,4934,4932,4931,243,4933,4935,4930],"class_list":{"0":"post-128150","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-medication","8":"tag-breaking-news","9":"tag-breaking-news-video","10":"tag-health","11":"tag-live-speeches","12":"tag-live-updates","13":"tag-live-video","14":"tag-medication","15":"tag-press-conference","16":"tag-real-time-coverage","17":"tag-video-updates"},"_links":{"self":[{"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/posts\/128150","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/comments?post=128150"}],"version-history":[{"count":0,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/posts\/128150\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/media\/64325"}],"wp:attachment":[{"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/media?parent=128150"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/categories?post=128150"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newsbeep.com\/us\/wp-json\/wp\/v2\/tags?post=128150"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}