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Treatment News
Inside the Pricing of a $300,000-a-Year Drug
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Thursday, January 10, 2013
Matthew Herper
Last night, NPS Pharmaceuticals announced that it was pricing Gattex, its drug for short bowel syndrome, at $295,000 per patient per year, about triple what analysts on Wall Street expected. It is the fourth drug approved in 2012 to be priced at more than $200,000 per patient per year. The others are: Kalydeco for cystic fibrosis (maker :Vertex Pharmaceuticals); Elelyso for Gaucher’s disease (Protalix and Pfizer); and Juxtapid for homozygous familial hypercholesterolemia (Aegerion Pharmaceuticals.) That represents 10% of the drugs approved by the Food and Drug Administration last year and a 44% increase in the number of such high-priced rare disease drugs on the market.








Francois Nader, the chief executive of NPS Pharmaceuticals, spoke with me this morning about how he and his team priced Gattex. Here is a roadmap for how a medicine can be priced at an annual cost equivalent to a house. These bullet points reflect NPS’ reasons for pricing the medicine as it did.
How, though, does anyone pay for such a medicine? The answer is that pricing of these rare disease drugs, known as ultra-orphan drugs in the biotech industry, are not paid for the way that most medicines are. Nobody buys them out of pocket, and the manufacturer refuses to grant discounts to insurers or to Medicare. Commercial insurers will usually not pay the whole cost of the drug, asking patients to cover a co-pay that could be 30% of the drug’s price. Through what is known as a co-pay assistance program, NPS will cover patients’ out-of-pocket costs. Nader thinks 51% of potential Gattex patients are on commericial insurance.
Another 34% of potential Gattex patients are on Medicare. For these patients, rare disease organizations will help pay the bill. NPS will give unrestricted grants to those rare disease organizations, but can’t say what they’ll be used for. Another 15% of patients probably won’t be able to pay at all. Those patients will get the medicine for free. NPS will have a field for of 38 people who will market the drug and get to know each patient personally and to negotiate insurance reimbursement for each drug. The general outline of this plan is similar to what is done by other rare disease companies like Alexion Pharmaceuticals, Sanofi’s Genzyme unit, and BioMarin. The strategy of targeting these rare diseases has been one of the most successful in biotech over the past decade; it has, for instance, made Alexion into one of the industry’s biggest stars. Nader says it cost about $250 million to develop Gattex, which is not that expensive in an industry where a drug can chew up $1 billion or more in development costs before getting approved.
Source: Forbes
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