Is a drug like Sovaldi worth it?

Recently I had separate discussions with 2 industry experts, and during those discussions the topic of Sovaldi came up. I was aware of the ongoing debate, and these conversations made me think about it further, and so I thought I would share my thoughts.

There have been many articles on this topic and most on the side that the drug is expensive and that insurance companies, and consequently the healthcare system, cannot afford it. There are several reasons why a drug may be worth the price including 1) the drug is tackling a life threatening disease, 2) the investment costs for the company to develop the drug, which as cited in literature keeps increasing and is on the order of around of billions of dollars, 3) if the drug is more effective than existing drugs in the market for that therapeutic area.

Beyond the above reasons, the patients are also paying for the innovation factor, just like a consumer would pay for a breakthrough innovative first in class product, such as the iphone, or the ipad or an LED TV screen. The current pharmaceutical paradigm is not sustainable (refer to my previous post, here), both in terms of economy/jobs and also bringing those innovative new medicines to market. Innovation is in demand, which is an investment in time and money. All the so called low hanging fruit of new therapies are gone, and now the industry has to reach further into the trees. Pharmaceutical companies can reinvest some of their profit from these “blockbuster drugs” into bringing more innovative medicines to the market that patients need. I propose that some attention also be placed on the profitability of insurance companies and their coverage of patients.

Can the question be asked, what price is too high? Yes, maybe. That same question can be asked for all innovative products. There might be a slight validity to that. Although if a drug is tackling a life threatening disease in the way that Solvadi is, essentially “curing” the disease with minimal side effects, I do not think you can make a strong enough case against it. A recent article puts the innovation factor into good perspective (check it out here). Gilead is also trying to do the right thing by bring costs lower in developing countries through collaborations with Indian Pharmaceutical companies (see article here). Another interesting article is in the Wall Street Journal (here).

Raja Krishnan, CA-AM, CLP

Business Development | NSF Engine | Academia - Industry Partnerships | Precision Medicine | Connector of Ideas to Ideas; People to Ideas; People to People

10 年

This is an interesting view (below article). Yes, there might be a debate about what is too high of a price to charge for drugs. Having said that, it depends on many factors. How many drugs for that therapy are on the market? Is it 1 or 5 or more? If there are many therapies and subsequent entrants do not provide significant improvement, then there should be a question. Also, what is the size of the market? Are there are multiple available therapies that provide the same efficacy? These are the cases that CMS Reimbursement can question. https://www.forbes.com/sites/matthewherper/2014/10/23/could-high-drug-prices-be-bad-for-innovation/

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Raja Krishnan, CA-AM, CLP

Business Development | NSF Engine | Academia - Industry Partnerships | Precision Medicine | Connector of Ideas to Ideas; People to Ideas; People to People

10 年

Oliver Yu: My suggestion is that it has been challenging enough for the FDA to maintain proper standards of the generic medicine. It would probably be even more challenging when there are different ways of re-importation to monitor. The volume would increase and there are different mechanisms and all the mechanisms would have to be controlled.

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Raja Krishnan, CA-AM, CLP

Business Development | NSF Engine | Academia - Industry Partnerships | Precision Medicine | Connector of Ideas to Ideas; People to Ideas; People to People

10 年

Oliver Yu, that is another good discussion about re-importation laws. My understanding is that the main resistance to this is being able to control the quality/efficacy of the product and prevent tampering. This will be extremely difficult to monitor if drugs are re-imported from countries across the world. At the same time there is enough instances where Indian Generic Pharmaceutical companies have sold poor quality products. There have been a lot of articles written on that as well and how that should be approached, an article from earlier this year: https://www.forbes.com/sites/theapothecary/2014/02/24/some-indian-generic-drug-companies-are-selling-shoddy-ineffective-medicines-to-u-s-patients/

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Oliver Yu

Exited Founder / Investor

10 年

The way I see it, Gilead Sciences gets to charge whatever the market can bear. What rankles me is that they charge 1% of the US price over in India. A functioning free-market would arb that until the prices come down in the US and the prices rise in India. But due to drug re-importation laws, arbitrage is illegal. Hence a net wealth transfer from US HepC suffers to Indian HepC suffers.

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