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Post Info TOPIC: NCHC Campaign to Reduce Sovaldi Costs


Guru

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RE: NCHC Campaign to Reduce Sovaldi Costs
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Zlikster wrote:

In ideal world life saving drugs would be forbiden to be in free market race...but seems we allowed free market economy to have 0 moral/ethics and we and whole biosphere on this planet will suffer greatly cause of it.


/rant over


It wouldn't even need to be an ideal world......just one where the complete lack of decency and compassion is not rewarded or regarded as a virtue.   Rage on, Zilkster.  :)



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Diagnosed in 2011, Incivek triple in 2011, tx discontinued, Genotype 1a, CT, VL 7mill, cirrhosis dx in 2012, age 67, waiting for new DAAs.



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skewedButNotBroken wrote:

Excellent read! In the Senate letter, they state that Sovaldi will be only $900 per treatment in India. I would start treatment tomorrow if I could get it for that price. Can you imagine...


 Hellow Carnivall??  I would like a 12 week vacation,  .........



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  HCV Genotype 3a , now Psot-Tx was on S/riba. First VL was 5.8 mil on 7-5-13 then "und" at 3.8 weeks. 06/13/14 still und. off meds 3 days back on 7/29 Last pill 08/10/14 SVR+4

 



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of course they increased cost to 84k$, those 11billion $ invested in purchase of Pharmasset have to be returned FAST ;)

Mind it, i still find 36k $ too much for a government sponsored/tax payers money research of this marvelous chemical taken/swaped into private hands for billions. That does not only includes Sofosbuvir yet all other overpriced meds.

I would love to see what the real cost, excluding marketing, of Sofosbuvir. Research, clinical trials, insurance, manufacturing, production, etc. Estimation is that production cost of Sofosbuvir is roughly 4$ per gram (each tablet is 400mg), so lets say 50cents per pill. Lets do for fun some numbers.

I know someone said it costs from 100mil-1bil$ for a new drug to be placed on market (up to 10years of research.trials). Lets say Sofosbuvir development costed 1bil $ (mind it, estimated value of Pharmasset was cca 3bil $). Considering there are round 3mil chronic hcv patients in USA, if everyone opted in for Sofosbuvir tx (most GT1, so lets say 3month tx, 84pills), thats 252mil pills with production cost of 126mil $+1bil $ of development cost = 1.256 mil $ / no. of patients 3 mil. =418$ per tx without profit, lets say they want 10 times profit, thats still 4k$ per patient cost of tx. Whole different story when someone buys a company for 11bil $ and wants ROI in first year (whats Gilead been doing). Still they could have easily sell it for 40k$ thats half the price they sell, still darn expensive, but they would be a) cheaper than other DAA b) wont be on all media news as most exp price per pill and be less perceived as greedy evil money loving company they are d) they could still sell to 3rd world countries with 99% discount and get a positive PR they badly need (they are doing it now tho) c) have ROI in 2 years, instead first year

Instead we got situations like this. My hepa is looking desperatly for her F4 relapse patients some Olyisio and Sovaldi and keep getting insane offers/prices. Like she received from Sovaldi distributor in Croatia, 120k EUR (168k $) for 168 pills (half that for 3 bottles). In Croatia average sallary is round 1k $, in Bosnia it's round 500$. What insurance can afford this price? what uninsured person can afford it? What govrnment in lower income countries can afford to subsidise this?

Antiretrovirals drugs for HIV real costs are 1$ per day (3pills in one), thats 360$ per year, but they sell em for 15k $ per year in USA and yet they block generic companies with all means to sell drugsto Africa where even 1$ per day is expensive. Production cost of antiretrovirals is simillar to hcv meds. Whats wrong with this planet? :( In ideal world life saving drugs would be forbiden to be in free market race...but seems we allowed free market economy to have 0 moral/ethics and we and whole biosphere on this planet will suffer greatly cause of it.


/rant over

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GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




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Excellent read! In the Senate letter, they state that Sovaldi will be only $900 per treatment in India. I would start treatment tomorrow if I could get it for that price. Can you imagine...



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Diag. with hep c in 1992; A3:F2;  GT 1a; IL28B CT; VL 900k, ALT 150, AST 100 on 8/5/2014; SOT 9/5/2014  S/O ---VL 127 after 6 days; VL detected on day 18 but < 15.; --> UND @ EOT+ 1 year SVR!



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This campaign for Gilead to reduce the costs of Sovaldi sprung up fairly recently.  The National Coalition on Health Care is primarily a lobbying group funded by insurance companies.   http://www.csrxp.org/

Two US Senators are on board, a Democrat and a Republican.  Here is the demand letter they sent to Gilead a few weeks ago: http://www.finance.senate.gov/imo/media/doc/Wyden-Grassley%20Document%20Request%20to%20Gilead%207-11-141.pdf

Here is an article about the Senate's involvement.  http://blogs.marke****ch.com/health-exchange/2014/07/11/gileads-high-pricing-of-sovaldi-draws-inquiry-from-senate-committee/

Note that Pharmasset intended to sell Sovaldi for 36K;  Gilead increased the cost to $84K.

I doubt this has Gilead is shaking in its boots, but it is interesting, nonetheless. 

 

 



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Diagnosed in 2011, Incivek triple in 2011, tx discontinued, Genotype 1a, CT, VL 7mill, cirrhosis dx in 2012, age 67, waiting for new DAAs.

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