Tahir Amin Profile picture
Sep 29, 2020 14 tweets 2 min read Read on X
Thread (1/14): Tomorrow, drugmakers will be testifying on the tactics the industry uses to prop up drug prices.

Let’s take a look at the story of a poster child of patent abuse: Celgene’s cancer drug Revlimid.
Currently, the list price for a 1-month supply of Revlimid is a staggering $22,314.

Revlimid is Celgene’s blockbuster moneymaker. In 2017, it brought in $8.1 billion — or 63% — of Celgene's revenue.

But, the real story of Revlimid starts back in the 1950s.
Revlimid began as the falsely proclaimed wonder drug Thalidomide, which was banished from the market in the early 60s after it was found to have devastating birth defects in the children of mothers who took it.
Thalidomide idled in the pharmaceutical archives for decades until in the early 90s AIDS researchers found it boosted part of the immune system.
Seeing an opportunity, drugmaker Celgene acquired Thalidomide and retooled it as Thalomid, a treatment for leprosy. Soon after, it used Thalidomide as a template to create Revlimid, a treatment for multiple myeloma, a rare form of blood cancer.
Now, in theory, our patent system exists to incentivize these types of breakthroughs by rewarding drugmakers like Celgene with a time-limited monopoly for their invention.
But drugmakers recognize that the system can be easily gamed, and if done so successfully, can be used to construct impenetrable patent walls around drugs that make it all but impossible for competitors to enter the market.
Celgene and its battalion of lawyers know this well. The main patent on lenalidomide (the active ingredient in Revlimid) expired in 2019, so to maintain their monopoly they got creative...
Recall, Revlimid is a relative of Thalidomide. Because of this, Celgene was required to create a patient safety programme (REMS). The programme includes videos and written materials for patients, protocols for doctors and pharmacies, and birth control requirements for women.
While intended as a way to protect patients, Celgene found a way to use this REMS programme to exploit them...
By filing a myriad of patent apps on its REMS programme, which competitors must use if they want to distribute an alternative, Celgene found a way to maintain its monopoly for decades after the expiration of its original patents.
To date, there are a staggering 196 patent apps on Revlimid. The 109 granted patents for Revlimid give Celgene over 42 years of patent protection. Remember, patent protection should only last for 20 years on an invention.
Egregious overpatenting should not be tolerated. Drugmakers like Celgene have gamed our patent system to monopolize life-saving medicines.

Yet while Celgene must be held accountable, the human and financial costs of this behaviour have already been incurred.
We have to ask the hard question: why does our patent system allow this in the first place?

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More from @realtahiramin

Dec 21, 2021
Another year of Covid. Another season without vaccine equity. Omicron, & whatever comes next, are the utterly predictable results of a lethal brew of racist/colonial structures and market-driven global health.

A year-in-review thread 🧵 (1/21):
In Nov 2020, before vaccines were even publicly available, the free market zealots at @WSJopinion were freaking out about countries in the Global South stealing IP rights for technologies that were supposedly too complex for them to make.
wsj.com/articles/a-glo…
It was an early attempt to set the tone.

@WSJ's neocolonial economics and racist industry talking points about global manufacturing capabilities needed debunking, which I did in this thread over a year ago. How do you feel now @WSJ?
Read 21 tweets
Nov 6, 2021
Next time you are thinking of using the word "innovation" in relation to the pharmaceutical industry or the patent system, or are involved in a debate about how reforming the patent system or negotiating drug prices will harm "innovation", think of this:
And this:
Read 17 tweets
May 10, 2021
Moderna's CEO on why he doesn't think waiving IP will increase mRNA vaccine supply: “If someone wants to start from scratch, they would have to figure out how to make mRNA, which is not in our patents.”

Right there, in black and white, are a few very important things. (1/10)
1. It confirms that Moderna’s statement in Oct 2020 about waiving patents was just PR stunt.

They deliberately left out the tech transfer part, and are saying here that the patents they would release wouldn’t be helpful anyways.
2. #TRIPsWaiver is only a prerequisite for expanding global manufacturing capacity.

It'll all come down to the details, and w/out tremendous pressure/scrutiny from the movement that made this happen in the first place those negotiations will ensure nothing substantive is done.
Read 10 tweets
May 10, 2021
Talking of candour, the following few sentences in this letter that caught my attention in particular:

“The proposed waiver for COVID-19 vaccines, threatens to disrupt the flow of raw materials.”
“It will unleash a scramble for the critical inputs we require in order to make a safe and effective vaccine.”
“Entities with little or no experience in manufacturing vaccines are likely to chase the very raw materials we require to scale our production, putting the safety and security of all at risk.”
Read 4 tweets
Nov 23, 2020
This @WSJ Editorial Board piece, which has the jingoism of Rudyard Kipling's writings, deserves a fuller response. But in this thread I'm going to focus on one particular sentence in the opinion to help enlighten the thinking of our 'friends' at the @WSJ. on.wsj.com/2IZPlFC
That sentence is:

"It’s not clear developing countries even have the ability to manufacture large-scale, complex technologies like Moderna’s mRNA vaccine or Eli Lilly’s monoclonal antibody cocktail—let alone distribute them."
Putting aside the @WSJ's superiority complex, it's worth looking at some examples in the past where similar statements made by those in the western hemisphere about the scientific/technological abilities of countries in the global south have been proven wrong.
Read 13 tweets
Sep 30, 2020
Despite what the CEO of Celgene/BMS has said in this hearing, it's important to note that even though Natco will enter with a generic version of Revlimid in 2022 it will be a very restricted amount.
The settlement between Natco/Celgene prevents Natco from fully coming to market until 2026. Other generics are still in litigation with Celgene BMS because of all the "important patent innovations" that Celegene piled up.
One of those "important innovations" is a patent on the crystalline form of lenalidomide which expires in 2027. A graduate student in organic chemistry would know how to get a crystalline form of a compound because it's just so obvious.
Read 4 tweets

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