Clinical Pharmacology & Therapeutics · 2012 · 156 citations · 2 references
PharmacyBiotechnologyPharmacologyDrug DesignMedical BiotechnologyProtein EngineeringBiologic TherapeuticsBiologic TherapiesBiosimilar RegulationNew Drug ApplicationsAccessAccess To BiosimilarsBiosimilar AffordabilityCommercialization Of BiospecimensHealth Care Affordability PolicyMarket Access For BiosimilarsPatent Term ExpirationRegulatory Frameworks For Biosimilars
The development of biologic therapeutics using advanced technology to copy and improve on nature's design of complex peptides, proteins, and glycoproteins has enabled the treatment of diseases in entirely new ways and brought unique and lifesaving treatments to many people. However, at least in part because of cost pressures, access to these truly amazing products has not been uniformly available; many patients do not qualify for these treatments, or the treatment is postponed until disabilities accumulate. The development of biosimilars--essentially copies of the original biologic drugs after patent expiration--allows for wider and, as important, earlier access to these agents because of their lower cost and consequently greater affordability. The development and commercialization of biosimilars can help address unmet medical needs by improving access to well-established therapeutic interventions while improving health-care affordability.
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Delivering affordable cancer care in high-income countries
Richard Sullivan, Jeffrey Peppercorn, Karol Sikora et al. · The Lancet Oncology · 2011 · 714 citations
Medicine, Health Policy, Oncology +14
Developing the Nation's Biosimilars Program
Steven Kozlowski, Janet Woodcock, Karen Midthun et al. · New England Journal of Medicine · 2011 · 196 citations
Pharmacy, Pharmaceutical Policy, Drug Approval Processes +15