Posted on July 1, 2019
10 most expensive drugs in the world
Research and clinical trials sometimes last for decades before the drug reaches its patients, and many substances simply don’t make it. Adverse and side effects or economic reasons can put an end to the whole research process overnight. When the number of patients affected by a condition is globally measured in thousands, or even only hundreds, the economic burden of research reflects on the treatment price- it reaches astronomical numbers. This article is a list of 10 most expensive treatments per patient in the world.
10. Spinraza (API Nursinersen)
Nusinersen (branded name Spinraza) treats a disease known as Spinal Muscular Atrophy (SMA). SMA occurs due to a mutation on a fifth chromosome (5q) characterized by progressive muscle atrophy that typically begins shortly after birth (although some forms of the disease have late onset). The drug comes in 12mg vials as a solution for injection. It’s given directly into the spine by specially trained personnel. The first dose is administered after the diagnosis, followed by one vial at 2, 4, and 9 weeks after the first one. After that, a maintenance dose is administered every 4 months for as long as the patient benefits of it.
The annual cost of treatment is $375,000 ($750,000 in the first year).
Manufacturer: Biogen, American multinational biotechnology company.
9. Lumizyme (API Alglucosidase alfa)
The drug is used for the treatment of Pompe disease (rare, inherited disorder). The disease is characterized by buildup of glycogen throughout the body, which ultimately leads to impaired function of the affected organs (predominately muscles and liver). It affects one in every 40,000 persons in the US. The drug is given as an intravenous infusion, 20mg per kilogram of body mass, every two weeks. The drug comes in 50mg vials with a price of $870.
Minimal annual cost of treatment is $520,000 (and can go up to $625,000).
Manufacturer: Sanofi Genzyme, MA, US.
8. Elaprase (API Idursulfase)
The drug is used for the treatment of rare inherited disease that affects only males- Hunter syndrome. Due to the inability to breakdown specific metabolic byproducts, they build up throughout body which cases walking and breathing difficulties. Without treatment, the symptoms become more severe over time. The dose depends on the patient’s body weight (0.5mg/kg), and the drug is given every week through slow intravenous infusion.
The price per vial (6mg) is $4,215, and annual treatment for a child that weights 35kg is $657,000.
Manufacturer: the Shire, a Biotechnology company from Ireland.
7. Brineura (API Cerliponase alfa)
Brineura is used to treat CLN2 disease (neuronal ceroid lipofuscinosis type 2 disease), a rare disorder that causes progressive brain damage. The drug is delivered every two weeks through a special device that runs from the outside of the skull to the region of infusion (inside the brain). The treatment lasts for as long as the patient benefits from it.
The annual cost of treatment reaches $700,000.
Manufacturer: US-based pharmaceutical company BioMarin Pharmaceutical Inc.
6. Soliris (API Eculizumab)
Eculizumab (brand name Soliris) is a drug used for the treatment of a rare group of diseases that affect red blood cells. It comes in vials as a solution for intravenous infusion. The dosage depends on the stage of treatment (initial or maintenance) and the patient’s body mass, so it’s may be administered anywhere from once a week to once every three weeks.
The cost per vial is $6,830 and, depending on the indication, the annual cost can reach up to $700,000.
Manufacturer: Alexion Pharmaceuticals Inc. USA
5. Carbaglu (API Carglumic acid)
The Carbaglu is used for the treatment of patients with elevated levels of ammonia in the blood. The indication area comes down to a handful of rare disorders, so the number of patients indicated for this kind of treatment is low. The dose ranges from 100 mg to 250 mg per kilogram of body mass, daily.
The price for 5 tablets (each containing 200 mg of active substance) is around $1,040, and depending on the severity of the condition, annual treatment cost can build up to $790,000 (although, typically it’s closer to the half of this price).
Manufacturer: Recordati, Italian pharmaceutical company.
4. Ravicti (API Glycerol Phenylbutyrate)
The drug is used to treat patients with urea cycle disorders (UCDs). Aside from precisely defined dosage and intake dynamics, patients who suffer UCDs need to adhere to a rigorous dietary regiment.
Ravicti comes as an oral solution in 25mL vials, with a price of $5,016 per vial. The body surface area and the patient’s age determines the dosage, so the annual cost of treatment can reach up to $794,000.
Manufacturer: Germany based pharma company Horizon Pharma GmbH.
3. Luxturna (API Voretigene neparvovec)
Luxturna treats adults and children with a specific kind of retinal dystrophy (mutations in gene RPE65). The drug is given as an intraocular injection after a few days of preparation (immunosuppressive medicines that reduce the chance of medicine being rejected by the patient’s body). Application of the drug is carried out in a highly controllable hospital setting by an experienced eye surgeon.
It is a one-time treatment with a price tag of $850,000.
Manufacturer: Novartis, Switzerland.
2. Glybera (API Alipogene tiparvovec)
Glybera was a gene therapy designed to treat a rare lethal disorder known as lipoprotein lipase deficiency. The treatment consisted of 60 intramuscular injections delivered in one session (the therapeutic effect was intended to last for at least 10 years). Known as the “million dollar drug” Glybera quickly gained infamy of the European public. Two years after approval in Europe, the manufacturer removed it from the market. Until 2018, only 31 patient worldwide received the treatment and its manufacturer (UniQure) has no plans of selling in North America anymore. This drug is a bitter reminder for pharmaceutical companies how decades of research can result in commercial failure.
1. Zolgensma (API Onasemnogene abeparvovec-xioi)
In May 2019, FDA approved new gene therapy for SMA, and with the price tag of $2,125,000 it’s the most expensive drug the world has ever seen. The drug comes in the form of suspension for intravenous infusion and targets children under the age of 2 with SMA, including those not showing the symptoms yet (the diagnosis is made through genetic testing). It’s the one-time treatment, and this is the argument that justifies such a high price- compared to the only rival on the market- Biogen’s Spinraza, Zolgensma provides a definitive cure for the disease. Having in mind the clinical research evidence collected so far, it might become a standard treatment for the SMA in the future.
It is a one-time treatment with a price tag of $2,125,000.
Manufacturer: Novartis, Switzerland.