Johnson & Johnson

Fix The Patent Laws Campaign (FTPL) launches global campaign urging Johnson & Johnson to reduce price of life-saving TB drug

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Fix The Patent Laws Campaign (FTPL), launched a global campaign today calling on pharmaceutical corporation Johnson & Johnson (J&J) to lower the price of its anti-tuberculosis medicine bedaquiline to no more than R15 per day for people everywhere who need it, in order to allow scale-up of drug-resistant TB (DR-TB) treatment and reduce deaths.

 

Doctors Without Borders (MSF), a member of FTPL demands this price cut considering the joint contributions made in the development of this drug, including by MSF itself. MSF was joined by TB activists and civil society in protests outside of J&J offices in the US, South Africa, Brazil, Belgium, Ukraine and Spain, demanding the corporation make the drug available for people with DR-TB for no more than “R15 a day”.

 

“Bedaquiline was developed using taxpayer money and contributions from the global TB community,” said Sharonann Lynch, HIV & TB Policy Advisor for MSF’s Access Campaign. “Those who contributed to bedaquiline’s development should have a say in how the drug is priced. We’re calling on J&J to price bedaquiline at no more than $1 per day so that it can be made available to all people with drug-resistant TB. We will not back down until the price of bedaquiline is brought down.”

 

Bedaquiline was developed with considerable taxpayer, non-profit and philanthropic support. Much of the critical work to inform the use of the drug and demonstrate its therapeutic value was conducted by the TB research community, health ministries, and treatment providers including MSF, and was financed by taxpayers and other donors. Despite this joint research and development effort by the global TB community, J&J alone owns the patent on the drug in many countries and has sole rights to determine in which countries the drug will be sold. Moreover, J&J also benefited from a significant financial windfall as it obtained a Priority Review Voucher* from the US Food and Drug Administration (USFDA), that can be used to get accelerated marketing approval for another of its drugs.

 

J&J currently charges double the price that MSF is asking: J&J has priced bedaquiline at approximately R6 000 for a six-month treatment course for countries eligible to buy the drug through the Global Drug Facility (GDF), a TB drug and diagnostic procurement mechanism, operating out of a UN agency. However, researchers from the University of Liverpool have calculated that bedaquiline could be produced and sold at a profit for much less – as little as approximately R3,75 per day if at least 108,000 treatment courses were sold per year. At no more than R15 per day, the price of bedaquiline would be R9,000 per person for the 20 months of treatment that many DR-TB patients require. In comparison, the lowest price J&J charges today for 20 months of bedaquiline is nearly R18 000 (R30 per day) in countries eligible to purchase through GDF, while J&J charges other countries much more. This high price affects the scale-up of the drug in many countries struggling with DR-TB epidemics, considering that bedaquiline is just one of multiple drugs required in treatment regimens.

 

“Bedaquiline saved my life. I was experiencing a lot of side effects during my previous treatment which included drugs that need to be injected,” said Noludwe Mabandlela, who was treated for multidrug-resistant tuberculosis (MDR-TB) in Khayelitsha, South Africa and was cured in early 2019. “After switching to bedaquiline, my health improved much faster. I wouldn’t wish anyone to go through what I experienced. Pharmaceutical corporations like J&J should stop inflating the price of the drug that offers a lifeline to people affected with drug-resistant forms of tuberculosis.”

 

Bedaquiline is one of only three new TB drugs to be developed in over half a century (the others are delamanid and pretomanid). The previously recommended DR-TB treatment regimens used by most countries required people to take as many as 20 pills a day for up to two years and endure painful daily injections and severe side effects ranging from psychosis and persistent nausea to deafness. These suboptimal treatments only managed to cure 55% of people with MDR-TB and just 34% of people with extensively drug-resistant tuberculosis (XDR-TB).

 

Based on data generated by the TB community showing improved treatment outcomes in people who received bedaquiline, the World Health Organization in 2018 recommended bedaquiline be used as a core part of an all-oral treatment regimen, replacing the injected drugs. Increased use of bedaquiline has already shown benefits, even among people more likely to have poorer treatment outcomes, including people living with HIV, and people with pre-XDR-TB and XDR-TB. For example: in Belarus, among 244 people who were treated with bedaquiline – 96% of whom had either pre-XDR-TB or XDR-TB – the treatment success rate increased to 87%.

 

Since WHO recommended the use of bedaquiline-a year ago-as a core drug for the treatment of MDR-TB, less than 12,000 people were treated with a regimen including bedaquiline according to national TB programmes. This is a paltry figure considering that an estimated 80% of the 558,000 people who develop DR-TB annually (Global TB report 2018) should be treated with this drug. Rapid rollout of better-tolerated treatment containing bedaquiline will happen only if J&J makes it widely available in an affordable way, including by allowing other TB drug manufacturers to make generic versions.




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