PBMs and 340B hospital markups driving up prices and foreign countries not paying their fair share. It’s time to crack down on middlemen and free riders.
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A dreaded patent cliff is looming for a number of key drugs positioned to topple over to the other side.
Some of pharma’s biggest wallops are still a few years off, such as the loss of a critical patent for Merck & Co.’s Keytruda in 2028. Other companies, like Pfizer, face a steady stream of blows as exclusivity for top-selling drugs fades away each year.
At AstraZeneca, two major losses are just months away. Before the year is out, the company will lose its market grip on Soliris, a rare disease drug, and Farxiga, a heart and diabetes medication, which pulled in over $10 billion in revenue last year combined.
Scoring new approvals will be critical to filling the gaps left by these blockbusters. So far this year, AstraZeneca is on a roll with its Daiichi Sankyo-partnered antibody-drug conjugates — a key component of its lofty goal to hit $80 billion in annual revenue by 2030. Today, we’re looking more closely at these FDA nods along with other standout drugs that recently crossed the regulatory finish line.
PharmaVoice readers who believed PBMs are to blame when drug prices become unaffordable for some patients. About 27% pointed the finger at pharma, while 21% said payers are liable.
Stronger connections lead to better outcomes. In this infographic, learn how to use key moments in the product lifecycle, from drug discovery to commercialization, to help transform patient care.