The Guardian Australia

Soon Covid-19 will be treatable, but it shouldn't just be the rich who benefit

- Jeremy Farrar Jeremy Farrar is director of the Wellcome Trust

We all want a cure for Covid-19, but it won’t come in a single drug. Neither can we expect to escape this global crisis if treatments, tests or vaccines are not made available to those most vulnerable worldwide. There’s a long way yet to go.

Robust research has shown that hydroxychl­oroquine, the drug once heavily promoted by Donald Trump, doesn’t work as a treatment. We wait in hope for the first vaccines but must be realistic: they may only provide partial protection, important as that will be. Now, as the US president pins his hopes on Regeneron’s antibody cocktail, it must be made clear: life can only return to normal with a range of clinically proven, effective treatments, tests and vaccines; the resilient health systems to deliver them; and the trust of the public.

More than a million people have lost their lives to the virus in just 10 months, and each day still brings a daily record of new cases. Others are suffering from “long Covid” and its debilitati­ng long-term effects. In the UK, as we head into winter, hospitalis­ations from Covid-19 rise and a new three-tier system of mini-lockdowns is introduced, we urgently need a range of high-quality treatments to protect people.

Though catapulted into the spotlight through Trump’s diagnosis, treatments have often been overlooked in favour of the much-coveted vaccines. To date, $2bn (£1.5bn) has been invested in vaccines – six times more funding than treatments. Yet the world needs $7.2bn just for effective treatments, without which millions more lives remain at risk. It’s a lot of money, but with the global economy expected to contract by $12tn in 2020 alone, it’s a fraction of what we are currently losing every day.

At the moment, there is only one proven treatment that reduces mortality from Covid-19: dexamethas­one. This widely available and affordable steroid has been used safely for decades, and can improve survival when used in patients in hospital with Covid-19 who need oxygen or are ventilated. But it does not work in those patients not on oxygen. We also know that the antiviral drug remdesivir can help speed recovery for severely ill patients, reducing the average hospital stay by around four days.

It is not surprising that months of research have led to so few treatments. We always expect many trials to fail. Our best shot in the short term has been to explore whether existing drugs show any benefit – trying everything from anti-malarial drugs to those used to treat arthritis. They are safe, affordable and easy to produce around the world. If they’re effective against Covid-19, we can ensure they will be accessed by those most in need in a matter of weeks.

For example, less than 20 days after dexamethas­one was identified as a treatment (by the UK-based Recovery trial), Unitaid, the World Health Organizati­on and Wellcome through the ACT-Accelerato­r global partnershi­p secured 2.9m treatment courses for low- and middle-income countries. The partnershi­p is poised to act immediatel­y there is clear evidence on safe and effective new treatments.

We must be realistic about what we can expect from repurposin­g drugs that have been designed for other diseases, but we should still exhaust all options.

Finding treatments that work across all stages of the disease – especially mild and moderate cases to stop progressio­n to more severe disease – would be a game-changer. In the limelight last week, monoclonal antibodies, the first treatments specifical­ly for Covid-19, could well be among them.

Trump has touted the benefits of Regeneron’s experiment­al monoclonal antibody cocktail, which has not yet finished its final clinical trials. Eli Lilly monoclonal antibody treatment also looks very promising. If successful, these could drasticall­y reduce the likelihood of mild symptoms becoming severe, as well as save lives for those with severe disease. There is huge potential.

In the 30 years they’ve been around, monoclonal antibodies have been transformi­ng the way doctors treat, prevent and cure serious noncommuni­cable diseases, including cancers and auto-immune disorders: last year, seven of the 10 bestsellin­g novel drugs were monoclonal antibodies for cancer and inflammato­ry diseases. But they are traditiona­lly among the most expensive treatments in the world: 80% are sold in the US, Europe and Canada, and few, if any, are available in low- and middle-income countries.

Covid-19 should be the catalyst to addressing the prohibitiv­e expense of these drugs and making them accessible for everyone. This will require new ways of thinking, technologi­cal innovation, new types of collaborat­ing and doing business, but I am confident that academia, industry and government­s around the world can find solutions together. This could transform the treatment of Covid-19 but also ensure the monoclonal antibody class of drugs are globally accessible and affordable for many diseases.

As the UK enters a critical winter, we should take stock of the many advances made since the start of the year. Medical staff now have experience of this disease: they know how to position patients, how to use fluids, how to stop the blood clotting and when to use ventilator­s. Their knowledge will prove invaluable as more people are admitted to hospital.

Alone, these measures and treatments will not be a magic bullet. But together, when combined with first-generation vaccines and essential public health measures to reduce transmissi­on, they give us every reason to be hopeful. In the near future, Covid-19 will be a preventabl­e and treatable disease. We must make this true for everyone, wherever they live or however rich they are. And whether they are a president or not.

 ?? Photograph: WPA/Getty Images ?? A scientist at work at the Oxford Vaccine Group’s laboratory.
Photograph: WPA/Getty Images A scientist at work at the Oxford Vaccine Group’s laboratory.

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