{"id":701911,"date":"2026-01-17T10:33:12","date_gmt":"2026-01-17T10:33:12","guid":{"rendered":"https:\/\/www.europesays.com\/uk\/701911\/"},"modified":"2026-01-17T10:33:12","modified_gmt":"2026-01-17T10:33:12","slug":"takeaways-on-turmoil-surrounding-fda-fast-track-drug-program","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/uk\/701911\/","title":{"rendered":"Takeaways on turmoil surrounding FDA fast-track drug program"},"content":{"rendered":"

WASHINGTON (AP) \u2014 A plan to slash drug review times at the Food and Drug Administration<\/a> is sparking deep concerns<\/a> among agency staffers and outside experts, with some saying the poorly defined effort<\/a> is taking key decisions away from career scientists and placing them in the hands of political leadership.<\/p>\n

The initiative by FDA Commissioner Marty Makary<\/a> promises ultra-fast reviews for drugs that align with \u201cU.S. national priorities.\u201d It\u2019s at the center of Makary\u2019s stated goal to \u201ccut red tape\u201d and \u201cchallenge assumptions\u201d at the agency tasked with assuring the safety of food, medicines, medical devices and other consumer goods.<\/p>\n

But FDA staffers say the push for faster approvals<\/a> is contributing to a climate of anxiety, fear and confusion within the agency\u2019s drug center, which has lost nearly 20% of its staff to recent layoffs, buyouts, retirements and resignations.<\/p>\n

Concerns about the legality of the program have also contributed to the recent departure of several leaders<\/a> of the FDA drug center<\/a>, which is now being led by its fifth director in the past year.<\/p>\n

FDA drug reviews have traditionally been handled by FDA career scientists who spend months analyzing data to determine whether drugs meet federal standards for safety and effectiveness.<\/p>\n

But the effort to truncate certain drug approvals has become intertwined with White House efforts<\/a> to secure pricing concessions for drugmakers, an unprecedented shift in the agency\u2019s longstanding science-based approach that staffers fear could damage the FDA\u2019s reputation and endanger patients.<\/p>\n

Health and Human Services<\/a> spokesman Andrew Nixon said the voucher program prioritizes \u201cgold standard scientific review\u201d and aims to deliver \u201cmeaningful and effective treatments and cures.\u201d<\/p>\n

Here\u2019s what to know:<\/p>\n

Top FDA officials have legal concerns about signing off on expedited approvals<\/p>\n

Questions remain among top FDA officials over who has the appropriate legal authority to sign off on drugs cleared under the Commissioner\u2019s National Priority Voucher program, according to several people with direct knowledge of the matter who spoke to The Associated Press on the condition of anonymity because they were not authorized to discuss confidential agency matters. <\/p>\n

The FDA\u2019s then-drug director, Dr. George Tidmarsh<\/a>, declined to sign off on approvals under the pathway. Tidmarsh resigned from the agency in November over a lawsuit challenging his conduct<\/a> on issues unrelated to the voucher program.<\/p>\n

After his departure, Dr. Sara Brenner, the FDA\u2019s principal deputy commissioner, was set to be the final decider on the approval decisions, but she also declined the role after looking further into the legal issues, according to the people. Currently the agency\u2019s deputy chief medical officer, Dr. Mallika Mundkur, is taking on the responsibility.<\/p>\n

Giving final approval to a drug carries significant legal weight, essentially certifying the medicine\u2019s safety and effectiveness meet FDA standards. If unexpected side effects or other problems later emerge, both the agency and individual officials could be pulled into investigations or lawsuits.<\/p>\n

FDA\u2019s voucher program has become intertwined with the White House drug pricing effort<\/p>\n

Despite such concerns, the program remains popular at the White House, where pricing concessions announced by President Donald Trump<\/a>, a Republican, have repeatedly been accompanied by FDA vouchers for drugmakers that agree to cut their prices.<\/p>\n

For instance, when the White House announced that Eli Lilly and Novo Nordisk would reduce prices on their popular obesity drugs, FDA staffers had to scramble to vet and announce new vouchers for both companies in time for the press conference, according to multiple people involved in the process.<\/p>\n

That\u2019s sparked widespread concern that FDA drug reviews have become malleable and open to political interference.<\/p>\n

Drug review decisions have been taken away from FDA career scientists<\/p>\n

FDA approval decisions have nearly always been handled by agency scientists and their immediate supervisors, rather than political appointees and senior leaders.<\/p>\n

But under the voucher program, approval comes through a committee vote by senior agency officials, according to multiple people familiar with the situation. Staff reviewers don\u2019t get a vote.<\/p>\n

Current and former staffers say the new approach flips FDA precedent on its head, minimizing the input of FDA scientists who have the greatest expertise and familiarity with the drug safety and effectiveness data.<\/p>\n

FDA reviewers report pressure to skip steps<\/p>\n

Because of the ambiguity around the program\u2019s workings, some drugmakers have had their own interpretation of the timeline for review \u2014 creating further confusion and stress among FDA staff.<\/p>\n

Two people involved in the ongoing review of Eli Lilly\u2019s anti-obesity pill<\/a> said company executives initially told the FDA they expected the drug approved within two months.<\/p>\n

The timeline alarmed FDA reviewers because it did not include the agency\u2019s standard 60-day prefiling period, when staffers check the application to ensure it isn\u2019t missing essential information. <\/p>\n

But Lilly pushed for a quicker filing turnaround, demanding one week. Eventually the agency and the company agreed to a two-week period.<\/p>\n

When reviewers raised concerns about some gaps in the application, one person involved in the process said, they were told by a senior FDA official that it was OK to overlook the regulations if the science is sound.<\/p>\n

Nixon declined to comment on the specifics of Lilly\u2019s review but said FDA reviewers can \u201cadjust timelines as needed.\u201d <\/p>\n

Lilly\u2019s CEO, David Ricks, told attendees at a health care conference on Tuesday that the company expects FDA approval of its pill in the second quarter of the year.<\/p>\n

___<\/p>\n

The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute\u2019s Department of Science Education and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.<\/p>\n","protected":false},"excerpt":{"rendered":"WASHINGTON (AP) \u2014 A plan to slash drug review times at the Food and Drug Administration is sparking…\n","protected":false},"author":2,"featured_media":701912,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[4315],"tags":[95897,112413,51,210982,32,5835,4179,175432,105,210985,98492,4326,33853,210984,6587,16,15,10673],"class_list":{"0":"post-701911","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-medication","8":"tag-andrew-nixon","9":"tag-ap-investigations","10":"tag-business","11":"tag-david-ricks","12":"tag-donald-trump","13":"tag-eli-lilly","14":"tag-general-news","15":"tag-george-tidmarsh","16":"tag-health","17":"tag-mallika-mundkur","18":"tag-marty-makary","19":"tag-medication","20":"tag-novo-nordisk-as","21":"tag-sara-brenner","22":"tag-u-s-food-and-drug-administration","23":"tag-uk","24":"tag-united-kingdom","25":"tag-washington-news"},"share_on_mastodon":{"url":"https:\/\/pubeurope.com\/@uk\/115909990985790896","error":""},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/posts\/701911","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/comments?post=701911"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/posts\/701911\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/media\/701912"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/media?parent=701911"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/categories?post=701911"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/tags?post=701911"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}