Biogen Idec’s Tecfidera (dimethyl fumarate) has been approved by the FDA for the treatment of people with relapsing forms of multiple sclerosis (MS).  The wholesale acquisition price for Tecfidera is reported to be $54,900,  about 9% less than the first MS pill, Gilenya (Novartis) that lists for approximately $60,000 per patient per year, but more than Sanofi’s MS Aubagio pill, which costs approximately$48,000 per year. Assuming these prices are relatively close to the actual WAC prices, an obvious question is “Why?”  Should these products all cost about the same or more than the 2011 median household income in the US of $50,054?

US Median household Income

US Median household Income

How sustainable are prices in this range? Can/will/should payers continue to pay no matter the price asked?

I am not selectively picking on these companies or on their products. The prices of these products are at a level that may lead people to ask questions related to  “How much to charge for health?”.  The answer to that question will not be in this blog but I will offer two  approaches to medicine pricing that some may find useful:

  1. Price it at a +/- X% difference to existing medicines depending on the comparative/relative medical value delivered
  2. Price it using the medical costs (cost-offsets) prevented or avoided by its usage

Both of these approaches assumes the medical value and/or cost-offsets can be measured and monetized.  Grand assumptions though these may be, they will be (if not arguably needed today)  fundamental to establishing medicine pricing and will be required data for registration (in some locales) and for pricing discussions.

Either of these two approaches offer a pragmatic and evidence-based methodology that should prove acceptable to both manufacturer and payer. Real world issues related to market life, ROI, social and shareholder responsibility, profitability, rationing, etc… will remain. Your suggestions for resolving these issue are welcomed and encouraged!

Tagged with: , , , , , ,

ohio_salamanderGo read “Macrophages are required for adult salamander limb regeneration”.

Unfortunately, gaining an understanding of the identity of the “…macrophage-derived therapeutic molecules…” that “..may therefore aid in the regeneration of damaged body parts…” could take quite a few years given the pace of  academic-based research.  What if, instead of having the academics write an application for  research funding year after tedious year, that some deep-pocketed pharma company picked up the tab and provided resources to accelerate the research?  Might real success happen sooner? Could damaged or missing body parts and organs be regrown in 10-15 years instead of 20-40? I’m all for seeking cures and treatments for other noxious diseases but being able to regrow a child’s missing leg or the kidney of a mom seems a worthwhile pursuit to me. Given that the regeneration process is likely somewhat preprogrammed, regeneration could potentially only need the right biochemical initiators and enablers to proceed.

I’m sure that some will write that what I’ve written is naive and unrealistic.  But, flying machines, walking on the moon, ball point pens, (pick your favorite first-world device/invention) were all ideas that were smiled at by those who knew better. There is no better time to start the journey to that future then today!

Tagged with: , , , , , ,
%d bloggers like this: