Source: The Conversation (Au and NZ) – By Elise Schubert, Pharmacist and PhD Candidate, University of Sydney
Australia currently has drugs that treat the symptoms of COVID, and drugs which have been repurposed from other diseases. Now the government has placed an early order for a new drug, sotrovimab, which works on COVID-19 virus particles in the body.
The federal government has bought 7,700 doses of sotrovimab (pronounced so-tro-ve-mab), with an initial delivery due some time this year.
But the COVID-19 Clinical Evidence Taskforce says the clinical trial results are too preliminary for the drug to enter routine use here. The taskforce says until further evidence shows sotrovimab is effective, it should only be given to patients as part of a human clinical trial.
What type of drug is it?
Sotrovimab is a newly developed monoclonal antibody-based medicine. This means it stops the action of the virus that causes COVID-19.
Antibodies are a type of protein in the immune system. Antibodies can recognise and attach to another type of protein called an antigen.
When an antibody attaches to the antigen, it triggers a series of reactions, which can be used to treat an associated disease.
How does sotrovimab treat COVID?
Sotrovimab works by binding to the spike protein on the outside of the COVID-19 virus. This is the same spike protein the body’s immune system is trained to recognise with the Pfizer COVID vaccine.
By binding to the spike protein, sotrovimab can block the virus from attaching to and entering human cells. This stops the virus replicating in the body.
How is sotrovimab given and what are the side effects?
The US Food and Drug Administration has approved sotrovimab for emergency use as an intravenous injection to treat COVID-19 patients at high risk of progressing to severe disease.
Sotrovimab can be given as soon as someone receives a positive test result or within ten days of getting COVID-19 symptoms.
The most common side effects with sotrovimab are rash and diarrhoea. Patients also need to be closely monitored for severe allergic reactions after the injection.
What have clinical trials shown so far?
In May 2021, pharmaceutical company GlaxoSmithKline released data from a clinical trial. It compared sotrovimab to a placebo in 583 at-risk COVID-19 patients to see whether it prevented the disease progressing to the extent that the patient needed to be hospitalised or died.
In the sotrovimab group (of 291 people), three patients saw their disease progress, compared to 21 in the placebo group (of 292 people). This amounts to an 85% reduction of disease progression in patients with mild to moderate COVID-19.
Has it been approved by medical regulators?
In May, both the US and European drug regulators authorised sotrovimab to be used in adults and children aged over 12 with mild to moderate COVID-19, but who are at a high risk of progression to severe COVID-19. This includes people aged over 65, and those with certain medical conditions such as heart disease, obesity, asthma, and diabetes.
Australia’s regulator, the Therapeutic Goods Administration (TGA), has received an application from GlaxoSmithKline to provisionally register the drug here in Australia, however its use remains limited to research settings.
So what does that mean for Australia?
The intention is to have the drug ready for use once approved by the TGA.
But the COVID-19 Clinical Evidence Taskforce, which creates clinical guidelines for the treatment of people with COVID-19 in Australia, has concerns about “the impact of sotrovimab on patient-relevant outcomes in the treatment of COVID-19” and the potential harms of unproven treatment.
It says sotrovimab should not be used outside randomised human clinical trials that have the appropriate ethical approval:
Trials are needed in special populations, including children and adolescents, pregnant and breastfeeding women, older people living with frailty and those receiving palliative care. Until further evidence is available, do not use sotrovimab for the treatment of COVID-19 in these populations unless they are eligible to be enrolled in trials.
As such, sotrovimab can only enter mainstream use in Australia when the full results of the phase 3 clinical trials are known. That data will be important for the TGA to determine whether the drug works, and whether it’s better than the current treatments.
Elise Schubert is a registered pharmacist at Royal North Shore Hospital, and a PhD Candidate receiving scholarship from the University of Sydney and Canngea Pty Ltd.
Dr. Lifeng Kang is a Senior Lecturer at the University of Sydney, School of Pharmacy. He received research funding from Australian and Singaporean research agencies, 3M Singapore, P&G Singapore, and some SMEs from Australia, UK, China and USA. He is the scientific advisor for Skinetrate Pty Ltd and Nusmetics Pty Ltd. He is a member of the following research societies: Australasian Pharmaceutical Science Association, Skin Research Society Singapore, Australasian Society of Dermatology Research, and an executive member of Transdermal Society in World Federation of Chinese Medicine Societies.
Associate Professor Wheate in the past has received funding from the ACT Cancer Council, Tenovus Scotland, Medical Research Scotland, Scottish Crucible, and the Scottish Universities Life Sciences Alliance. He is Fellow of the Royal Australian Chemical Institute and a member of the Australasian Pharmaceutical Science Association. Nial is science director of the medicinal cannabis company Canngea Pty Ltd, a board member of the Australian Medicinal Cannabis Association, and a Standards Australia committee member for sunscreen agents.
– ref. What is sotrovimab, the COVID drug the government has bought before being approved for use in Australia? – https://theconversation.com/what-is-sotrovimab-the-covid-drug-the-government-has-bought-before-being-approved-for-use-in-australia-165802