Drugmaker AstraZeneca is now injecting people with its new antibody treatment for Covid-19 in a bid to see if it will protect people and also help the already sick.
The company, which is also manufacturing a vaccine hopeful made by Oxford University scientists, hope the treatment will be a coronavirus breakthrough.
Called monoclonal antibody therapy, the treatment works by pumping antibodies – natural virus-fighting molecules – into people who don’t have their own.
These antibodies are harvested from others who have already had the disease and produced the right substances to fend it off.
If AstraZeneca’s therapy works it could be a way to equip people’s immune systems to fight the coronavirus, even if they have never had it.
The British company, worth £114billion, confirmed that the treatment has now started human trials in a group of 48 adult volunteers in the UK.
The pharmaceutical company AstraZeneca is trialling a treatment based on cloned immune system antibodies from people who have already recovered from Covid-19
AstraZeneca said the drug – known as AZD7442 – is a combination of two monoclonal antibodies.
Antibodies are substances produced by the immune system which it uses to tackle an invader such as a virus and then they store the memory of how to fend it off.
The presence of a specific type of antibody in someone’s blood – for Covid-19, for example – usually indicates someone has already had a disease. Sometimes it means they are unlikely to get it again, but it is not clear if this is the case for coronavirus.
Monoclonal antibody therapy works by harvesting these antibodies from people who have already had coronavirus, and cloning them in a lab.
The cloned antibodies are then put into a solution and injected into a patient who has not had Covid-19, to boost their immune system.
It boosts the immune system because the therapy means that if someone is exposed to the virus or has already caught it, their body effectively receives a batch of extra soldiers to fight it off.
The antibodies were discovered by Vanderbilt University in Nashville, Tennessee, and then licensed to AstraZeneca in June.
The company then genetically engineered the combined antibodies so that they ‘afford at least six months of protection from Covid-19’.
AstraZeneca said its trial, which will include up to 48 healthy volunteers in the UK aged 18 to 55, will look at the safety of the treatment, as well as the body’s reaction to the drug and how it processes it.
It hailed the move an ‘important milestone’ and said the drug has the potential to both protect uninfected people and to help people who are already sick.
Monoclonal antibody therapy works by injecting a person with antibodies which bind onto the coronavirus and stop it being able to latch onto cells in the body
Mene Pangalos, vice-president of research and development at the firm, said: ‘This trial is an important milestone in the development of our monoclonal antibody combination to prevent or treat Covid-19.
‘This combination of antibodies, coupled to our proprietary half-life extension technology, has the potential to improve both the effectiveness and durability of use, in addition to reducing the likelihood of viral resistance.’
If the initial trial is successful – that is, the drug appears to be safe and effective – the company plans to move on to larger phase two and three human trials.
The trial is being funded by the US Defence Advanced Research Projects Agency and the Biomedical Advanced Research and Development Authority, which is part of the US Department of Health and Human Services.
AstraZeneca’s announcement comes after the company yesterday fended off claims that the US was trying to strike a deal to get access to its Covid-19 vaccine before clinical trials had finished.
The company issued a denial amid reports Donald Trump wants to get the jab approved before the presidential election this autumn.
White House insiders claimed the US President is considering speeding up regulatory approval for the jab, originally developed by Oxford University scientists.
Getting a vaccine into use and slowing down the US’s devastating coronavirus crisis — the worst in the world — could boost Trump’s chances of becoming re-elected in November, when he runs against Democratic candidate Joe Biden, who accused him of having ‘failed to protect us’.
But AstraZeneca, which oversees manufacturing and distribution of the jab, said it has not entered any talks about getting it an emergency use authorisation in the US. It added that it would be ‘premature to speculate on that possibility’.
A spokesperson for the firm said: ‘AstraZeneca has not discussed emergency use authorization with the US government and it would be premature to speculate on that possibility.
‘Late stage Phase II/III trials for AZD1222 are ongoing in the UK and other markets globally, and we do not anticipate efficacy results until later this year.’
Number 10 yesterday insisted Britain will be the first to get the Covid-19 vaccine, if it is proven to work.
The UK has already bought 100million doses of the jab, while the US has ordered 300million.
Early trials have shown promising results, with tests showing the vaccine is safe to use in humans and appears to provoke an immune response.
But data that proves it protects people is not expected until later this year.