-
Mashup Score: 1
The House Appropriations Agriculture, Rural Development, and FDA Subcommittee advanced the FDA’s fiscal year 2025 funding bill, beginning a likely long and difficult budget cycle.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 1Accelerated Approval: Withdrawing Gene Therapies Could Be Easier Than Small Molecules - 6 month(s) ago
The FDA would only withdraw a rare disease gene therapy for “pretty clear” reasons, such as when there is minimal benefit with extensive side effects. The one-and-done nature of administration also makes withdrawal easier, CBER Director Peter Marks says.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 1
The agency seeks feedback at a 13 June virtual hearing on three general topics related to advisory committees: panel composition, barriers to service for Special Government Employees, and public perception and understanding of the adcomm process.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 1US FDA Drugs Center Launches Clinical Trial Innovation Hub With Demonstration Projects - 7 month(s) ago
CDER’s Center for Clinical Trial Innovation (C3TI) will support innovative clinical trial approaches designed to improve the quality and efficiency of drug development and regulatory decision-making. The initiative includes demonstration projects on Bayesian analyses, selective safety data collection and point-of-care trials.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 1Amylyx’s Relyvrio Withdrawal May Trigger More Public Pledges Based On Confirmatory Trial Data - 7 month(s) ago
Company makes good on vow at a September 2022 advisory committee meeting to withdraw the ALS drug if the PHOENIX trial failed. That pledge served as a backstop to FDA’s approval decision based on a single study and created a level of sponsor accountability that often is missing when postmarketing studies fail.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 1US FDA Wants Advisory Committee Duty To Be ‘Enjoyable’ - 8 month(s) ago
Advisory committee reform efforts include streamlining the selection and onboarding processes, in part to understand that members often have other professional priorities, Principal Deputy Commissioner Namandjé Bumpus said.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 1Alzheimer’s And Surrogate Endpoints: FDA’s On A Case-By-Case Basis Per New Guidance - 8 month(s) ago
After Aduhelm and Leqembi rendered the 2018 guidance moot, FDA formally acknowledges the possibility of using surrogate endpoints for accelerated approval in Alzheimer’s in updated draft but says acceptability of the any endpoint will depend on details of specific therapeutic program.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 2Amylyx’s ALS Drug Relyvrio Fails In PHOENIX Confirmatory Study, Setting Up Withdrawal Question - 8 month(s) ago
Company will meet with regulators and the broader ALS community to discuss top-line results and make ‘informed decisions,’ which may include voluntary withdrawal. During FDA review, Amylyx had pledged to remove Relyvrio if PHOENIX failed.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 2
OCE Director Richard Pazdur was less sanguine, however, noting that while the Pepaxto withdrawal may have been faster than others, it still required more than 60 meetings to complete.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
-
Mashup Score: 3Aduhelm’s Post-Marketing Studies: At Least One More Data Dump Likely Required By NIH - 9 month(s) ago
Pulling the controversial Alzheimer’s drug’s BLA should not exempt Biogen from fulfilling ClinicalTrials.gov reporting requirements for two key studies, even if the research gets terminated, former head of the NIH data repository tells the Pink Sheet.
Source: pink.citeline.comCategories: General Medicine News, Rare DiseaseTweet
RT @PharmaPinkSheet: US FDA May See Second Straight Year of Non-User Fee Funding Cuts From Congress https://t.co/WjXLJwzjHr #PinkSheet