Pharmaceutical Executive
The reauthorization of the Prescription Drug User Fee Act (PDUFA) comes but once every five years. Set to expire September 30-and with congressional Democrats riding high and consumer confidence in drug safety at record lows-the deal by which pharma pays FDA to review its products is in for a long hot summer of debate.
The reauthorization of the Prescription Drug User Fee Act (PDUFA) comes but once every five years. Set to expire September 30—and with congressional Democrats riding high and consumer confidence in drug safety at record lows—the deal by which pharma pays FDA to review its products is in for a long hot summer of debate. • The line of merry pols and other souls, including industry lobbyists, patient advocates, and FDA bigwigs past and present, who are hanging their wish lists on this post-Vioxx PDUFA is already mighty long. By the time the bill finally rolls out for a vote, it's bound to be as big as a Rockefeller Center Christmas tree. • On April 18, the Senate Committee on Health, Education, Labor, and Pensions (HELP) made some headway by passing "Kenzi"—a bill from Ted Kennedy and Mike Enzi that sharpens the agency's teeth when it comes to monitoring drug safety, while shaking down pharma for 45 percent higher user fees. • Kenzi is widely viewed as the best-bet compromise between, on the one hand, PDUFA IV, the FDA–pharma proposal that merely tweaks the status quo, and, on the other, sweeping agency makeovers, including a competing Senate bill from Chris Dodd and Charles Grassley that calls for a brand-new safety center. Oh, and there's a growing chorus singing a "Kill PDUFA" carol. • We thought we'd play Santa's helper and provide a guide to the most eye-catching balls—er, bills.
Novel GLP-1 Receptor Agonist Demonstrates Promising Results Treating Patients with Obesity
January 21st 2025Data from a Phase Ia single ascending dose study found that ASC30 demonstrated dose-proportional pharmacokinetics, a half-life of up to 60 hours, and superior pharmacokinetic properties compared to other oral GLP-1 receptor agonists.
What Every Pharma CEO Should Know About Unlocking the Potential of Scientific Data
December 11th 2024When integrated into pharmaceutical enterprises, scientific data has the potential to drive organizational growth and innovation. Mikael Hagstroem, CEO at leading laboratory informatics provider LabVantage Solutions, discusses how technology partners add significant value to pharmaceutical R&D, in addition to manufacturing quality.
Key Findings of the NIAGARA and HIMALAYA Trials
November 8th 2024In this episode of the Pharmaceutical Executive podcast, Shubh Goel, head of immuno-oncology, gastrointestinal tumors, US oncology business unit, AstraZeneca, discusses the findings of the NIAGARA trial in bladder cancer and the significance of the five-year overall survival data from the HIMALAYA trial, particularly the long-term efficacy of the STRIDE regimen for unresectable liver cancer.
FDA Approves Amgen’s Lumakras Plus Vectibix for KRAS G12C-Mutated Metastatic Colorectal Cancer
January 20th 2025Approval is based on data from the Phase III CodeBreaK 300 trial, which demonstrated that treatment with Lumakras and Vectibix significantly improved progression-free survival in patients with KRAS G12C-mutated metastatic colorectal cancer.