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Starting in January, multiple biosimilars of AbbVie’s blockbuster drug Humira are set to flood the US pharmaceutical market. The arrival of Humira biosimilars is expected to provide cost-effective alternatives to the anti-tumor necrosis factor (TNF) biologic, but their eventual position on the market remains to be seen.
A push for biosimilars. 2021 will see simplified requirements for biosimilars being implemented. Companies can let AIFA know about biosimilars coming to market giving 30 days notice from the end of the originator patent. Lower paybacks possible. The Italian industry makes regular paybacks when spending ceilings are breached.
However, low-cost generic and biosimilar manufacturers are likely to be particularly exposed to these economic pressures. By downloading this Report, you acknowledge that we may share your information with our whitepaper partners/sponsors who may contact you directly with information on their products and services.
However, low-cost generic and biosimilar manufacturers are likely to be particularly exposed to these economic pressures. By downloading this Report, you acknowledge that we may share your information with our whitepaper partners/sponsors who may contact you directly with information on their products and services.
Department of Health and Human Services (HHS) recently published a WhitePaper on Policy Considerations to Prevent Drug Shortages and Mitigate Supply Chain Vulnerabilities in the United States —with input from several HHS stakeholders, including FDA, CMS, and the Administration for Strategic Preparedness and Response. By Kalie E.
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