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Prescription drug costs are a urgent concern for both consumers and policymakers. FIGURE 3-2 (A) Medicare Part D generic drug worth tendencies for all generics and established generics (first quarter 2010 to second quarter 2015). The light blue line represents the composite development of generic medication (established basket”) present available in the market throughout the analysis period, whereas the dark blue line represents these generics (changing basket”) that came into and exited during the period. (B) The variety of established medicine underneath Medicare Part D that skilled a rare worth increase, first quarter 2010 to first quarter 2015.
It is value considering how a conditional approval process might transform the economics of pharmaceutical innovation. Immediately, GLP-1 analogues achieve nearly $2 billion in annual sales per drug, and analysts mission comparable sales for accredited antiobesity drugs. Utilizing these figures, we modeled the impact of an FDA policy that offered conditional approval to such pharmaceuticals, restricting their use to the ten % of overweight or diabetic sufferers whose conditions have been most serious and most immune to current therapies. Selling to solely 10 % of a drug's $2 billion market would yield a $200 million alternative — not too removed from the common price of Phase III trials for antiobesity ($254 million) and GLP-1 ($187 million) drugs. In different words, a conditional approval strategy would let firms largely recoup the prices of later Section III trials.
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