The latest news on US FDA user fee decisions and submissions to the agency.
The US Food and Drug Administration's Center for Drug Evaluation and Research has now given the nod to 38 novel agents in 2019 after issuing a trio of significant approvals to Novartis AG's Adakveo (crizanlizumab-tmca), BeiGene Ltd.'s Brukinsa (zanubrutinib) and Shionogi & Co. Ltd.'s Fetroja (cefiderocol).
If fact, there was so much news this week, we couldn't keep track of it all in one place. See...
A real-world evidence study also does not meet the regulatory standard for an adequate and well-controlled clinical investigation, the agency said. The FDA should allow the accelerated approval drug to remain available like other treatments that failed their confirmatory trials, Intercept said.
Recent and upcoming US FDA advisory committee meetings and a summary of the topics covered.
New marketing authorization applications filed with the European Medicines Agency's human medicines committee (the CHMP) for review under the EU's centralized procedure. Updated monthly.
Proposal to have panelists rate the strength of efficacy and safety evidence on a numeric scale also draws support in written comments on ways to optimize the advisory committee process.
A real-world evidence study also does not meet the regulatory standard for an adequate and well-controlled clinical investigation, the agency said. The FDA should allow the accelerated approval drug to remain available like other treatments that failed their confirmatory trials, Intercept said.
Stay up to date on regulatory guidelines from around the world with the Pink Sheet's Guidance Tracker. The complete Global Pharma Guidance Tracker, with sortable and searchable listings going back to 2014, is available online.
Recent and upcoming US FDA advisory committee meetings and a summary of the topics covered.
