Yesterday the president
personally rolled out an "Advance Notice of Proposed Rulemaking (ANPRM)” regarding "International
Pricing Index Model for Medicare Part B Drugs.” This is DC-speak for “this is
what I plan to do about high drug prices.” The proposal is focused on those
Medicare drugs that are administered in hospitals and physician offices (“Part B,” as opposed to drugs bought at the pharmacy, or “Part
D”). Currently,
physicians are reimbursed 106 percent of the average sales price (ASP) for
drugs they administer to their patients.
The core of the proposal is to make two changes. First, hospitals, doctors, and
other providers will be reimbursed a fixed fee to cover the cost of
administration. Notice that with the fixed fee (instead of 6 percent of the
drug's ASP), they have no incentive to seek higher drug prices. Second, they
will purchase the drugs from any drug vendor who wants to get into the business
of buying from pharmaceutical manufacturers and selling to the hospitals and physicians. For every sale, the vendor will be paid 126 percent of the International Price Index (IPI)
for the drugs. Notice that the vendors have every reason to negotiate low
prices (and pocket the difference with the fixed 126 percent of the IPI)
with the manufacturers.
Now comes the important part. As a stylized fact, drug prices are lower around
the globe than in the United States; the price in the U.S. is about 180
percent of the average overseas. So, taken at face value, the change is an
enormous cut in prices in the United States and pressure for negotiation
down. What can a drug maker do? Raise prices abroad to make up the difference.
The system — in principle — is supposed to move toward equalizing prices,
retaining sufficient profitability for pharmaceutical companies, and spreading
the (expensive) costs of research and development more equally across the
globe.
As an example, suppose a drug is sold for $200 in the United States
and $100 abroad. In simple terms, the drug company
is paid $300 for the two sales and Medicare is paying $212 for the treatment. If the new reimbursement is immediately applied,
the hospital in the
United States will get the fixed fee,
say $12. The vendor will get $126 so Medicare pays a total of $138 and saves money. The
vendor will be willing to pay $126 or less to the drug
company; let's say they bargain down to $120. Suddenly revenue to the drug manufacturer is only $220 instead of $300.
This cannot persist.
The Trump Administration's dice roll is that the drug manufacturer can get the
international price and domestic price to equalize at $150. If so, research and development can continue as before. At that
price, Medicare is paying only $201 (126 percent of $150 plus $12) — less than the $212 currently. And the vendors can compete to be the supplier and keep the markup from $150 to $189.
But that is a BIG if. Countries around the globe have low prices because they
have consistently told manufacturers to take the low price or simply not be
able to sell. That is one reason that 90 percent of new drugs are available to U.S. patients, but only two-thirds are available
in the U.K., one-half in France and
Canada, and one-third in
Australia. If international prices don’t change, the new formula will
effectively import their price controls to the Medicare system. With
artificially low prices, the money will have to come from somewhere else —
commercial insurers in particular — or drugs will simply not be available and
U.S. patients will pay in the most fundamental terms.
There are a million other details and questions about the proposed
demonstration — measuring prices accurately, picking the comparison countries,
deciding which drugs will be in the demo, deciding which areas will be in the
demo, and so forth. Those will all matter. This is a dramatic and
risky proposal that needs a lot of specifics and details to be truly
assessed well.
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