New Marijuana-Based Epilepsy Treatment to Cost $32,500 a Year

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burnin1

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From The Wall Street Journal

New Marijuana-Based Epilepsy Treatment to Cost $32,500 a Year
epidiolex.jpg

GW Pharmaceuticals CEO says the price was set to be in line with other brand-name epilepsy drugs

By Peter Loftus Aug. 8, 2018

GW Pharmaceuticals GWPH -2.05% PLC said it plans to charge about $32,500 per patient annually in the U.S. for its new treatment for rare forms of epilepsy, the first prescription drug derived from the marijuana plant.

The U.S. Food and Drug Administration approved Epidiolex, also known as cannabidiol, in June to reduce seizures associated with forms of epilepsy known as Lennox-Gastaut syndrome and Dravet syndrome, in patients 2 years of age and older.

GW Pharmaceuticals, based in the U.K., makes cannabidiol from a proprietary strain of cannabis designed to maximize a therapeutic component while minimizing components that produce euphoria or a high.

Chief Executive Justin Gover said in an interview Wednesday that the company set the price to be in line with other brand-name epilepsy drugs, such as H. Lundbeck A/S’s Onfi. He noted that the FDA designated the product an “orphan drug,” meaning it treats rare conditions, and that some other orphan drugs carry higher prices.

“We wanted to make sure we were pricing Epidiolex in such a way where the means to access this medication would be consistent with branded epilepsy drugs these patients already use,” he said.

Out-of-pocket costs for patients taking Epidiolex could range from $5 to $10 a month for those in state Medicaid programs to as high as $200 a month for some private insurance plans, Julian Gangolli, president of the company’s North America unit, said on a conference call with analysts Tuesday. Uninsured patients may qualify for receiving the drug free.

Dr. Jacqueline French, chief scientific officer of the Epilepsy Foundation, said there are low-cost generic epilepsy drugs on the market, but many patients with the rare forms of the disease have already tried them and the drugs didn’t help much.

Dr. French said Epidiolex improved symptoms for many children in clinical trials, and she is happy the price isn’t significantly higher.

The company expects to make the drug available after the U.S. Drug Enforcement Administration assigns it a controlled-substance classification, a decision expected by late September. GW Pharmaceuticals will distribute the drug through specialty pharmacies that ship directly to patients and caregivers.

https://www.wsj.com/articles/new-marijuana-based-epilepsy-treatment-to-cost-32-500-a-year-1533761758
 
That is a totally bullshit and biased post.

That's like talking about something that has a SUGGESTED RETAIL PRICE of 32k but a selling and/or 'street' price of $200 a month.

This is what I mean about how the news is written to enforce someone else's opinion and agenda.

I wonder how much that company spent on research to develop that drug. EDIT: I went and looked it up. GW SPENT ONE BILLION dollars in research on this and other drugs their company developed.

A BILLION DOLLARS

But, since everyone thinks the company is a rip off, maybe we should go back in time and tell this company NOT to spend that money on research and just let all these children suffer with the epilepsy. Tell them to make a better beer instead. A really CHEAP beer, right gang?

I think news like this is so unfair and biased.
 
That Billion dollar research stat is so misleading. The research for all drugs for as long as the company has been in existence perhaps.

People will not flock to this drug if they have homemade or dispensary bought remedies that they can afford.

In 2016 GW predicted the price would be from 30K t0 60K a year. The price turned out less than they predicted the price would be. Still too much for most who need it.
GW Pharmaceuticals made this drug for profit. Not to help people. They will make money believe me.

Yes it is a ripoff. If a drug is made that is not affordable to most of society, then it is useless to most of society.
 
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