-
ChemoCentryx's Drug Gets U.S. FDA Nod For Treating Rare Autoimmune Disease Opens in a new window)
The drug, avacopan, which will be available under brand name Tavneos in the next few weeks, will have a wholesale price of between $150,000 and $200,000 per patient per year. -
Europe’s Largest Clinical Trial Sponsors Are Getting Better at Reporting Results Opens in a new window)
The 26 research institutions have run nearly 4,600 trials testing medicines and, so far, 641 sets of results have been made available.Comments
-
Government Price Controls Will Kill Pharma Innovation, Lilly CEO Says Opens in a new window)
America is the cradle of breakthrough pharmaceutical innovation. U.S. biopharmaceutical companies create nearly two in every three new medicines.Comments
-
Merck Sells Federally Financed Covid Pill to U.S. for 40 Times What it Costs to Make Opens in a new window)
The Covid-19 treatment molnupiravir was developed using funding from the National Institutes of Health and the Department of Defense.Comments
-
Eli Lilly CEO: Drug Pricing Bill Would 'Fundamentally Restructure' Company
Eli Lilly CEO David Ricks joins CNBC's Meg Tirrell to discuss how a pending drug pricing bill would "fundamentally restructure" the company's business model.Comments
-
Merck’s Covid-19 Drug Is a Boon for Wall Street and Main Street Opens in a new window)
Antiviral drugs that keep some coronavirus patients out of the hospital are badly needed, and investors know it.Comments
-
The U.S. Can Lower Drug Prices Without Sacrificing Innovation Opens in a new window)
Large pharmaceutical companies are nowhere near as important to real drug innovation as they purport to be.Comments
-
Merck’s New Covid-19 Drug Could be One of the Most Lucrative Drugs Ever Opens in a new window)
The drug, named molnupiravir, reduces the risk of hospitalization or death by 50% in Covid-19 patients with mild and moderate symptoms compared with placebo, Merck said.Comments
-
Virtual Event
The evolving landscape for biosimilars.Comments
-
Understanding the Aducanumab (Aduhelm) Approval in the US
This lecture will describe the US FDA approval of aducanumab (Aduhelm) for Alzheimer disease and the implications the approval has had across the US health care system.Comments
-
Germany Decides On Added Benefit Of Gilead’s Veklury For COVID-19 Opens in a new window)
The body in charge of pricing and reimbursement in Germany has downgraded the extent of additional benefit offered by Gilead’s Veklury for treating COVID-19 patients.Comments
-
Picture Is Worth 1,000 Meetings: ‘Snapshots’ Could Support ‘Breakthrough’ Dialogue At US FDA Opens in a new window)
US FDA’s Oncology Center of Excellence is eager to pilot test ‘Drug Development Snapshots’ as a potential tool to optimize communication for drugs receiving the Breakthrough Therapy Designation.Comments
-
Real-World Evidence Under Consideration For Use In Interchangeable Biosimilars Applications Opens in a new window)
US FDA research funded under BSUFA III will investigate what kind of safety data is needed for interchangeability.Comments
-
What's Fueling the World's Covid-19 Vaccination Disparity?
Amnesty international has warned covid-19 developers not to put profits before lives.Comments
-
A W.H.O. Panel Recommends Treating High-Risk Covid Patients with Monoclonal Antibodies. Opens in a new window)
In the United States, some health experts have worried that promoting the therapy, which the government covers at a cost of $2,100 per dose, was taking away time and money from the effort to get more Americans vaccinated against Covid.Comments
Comments