SWITZERABD,:The World Health Organization said Friday that it had prequalified the arthritis treatment tocilizumab for use in patients hospitalised with severe COVID-19, in a bid to increase access to the pricey drug.
The monoclonal antibody, used in anti-inflammatory drugs made by Swiss pharma giant Roche, has been shown to reduce the risk of death and also hospitalisation time in certain patients suffering from severe COVID.
WHO has, like the United States and the European Union, already recommended its use to treat severe COVID in hospital settings.
But it remains in short supply and is very expensive -- a single dose reportedly goes for up to $600 in lower-income countries, WHO said, adding though that its prequalification should help make it more accessible.
The UN health agency said it had added three different compositions of the monoclonal antibody to its list of prequalified treatments for the pandemic disease, in a move aimed to spur more the production of more cheaper generic versions.
Prior to tocilizumab, the WHO has prequalified three different compositions for the steroid dexamethasone for treating COVID, as well as Gilead’s antiviral remdesivir, although that prequalification has since been suspended.
Tocilizumab has previously been authorised mostly for the treatment of arthritis in about 120 countries.
But during the pandemic, it has also been shown to suppress a dangerous “cytokine storm” -- the over-reaction of the immune system to the coronavirus. WHO pointed out that the patent for tocilizumab had expired for most uses.
This, it said, “means there should be no intellectual property barriers,” although it warned there was “low global availability for quality-assured biosimilars of the product”.
WHO said it was currently discussing with Roche how to lower prices and improve access in low- and middle-income countries. - THE HINDUSTAN TIMES
Add new comment