The company said in a statement that it is focused on processing previously approved requests, and that it is developing a new system that it says will allow patients to get the drug in a similar timeframe to what it would have taken to work through the requests it has received.
It will make exceptions for pregnant women and children under 18 years of age with confirmed Covid-19 and “severe manifestations” of the disease.
The company said in its statement that “enrollment in clinical trials is the primary way to access remdesivir to generate critical data that inform the appropriate use of this investigational medicine.”
Gilead said that in recent weeks there has been “an exponential increase” in requests for compassionate use because of the spread of the coronavirus in Europe and the U.S. This has “flooded” its treatment access system, which was set up for very limited access to the medicine and was, it said, “never intended for use in response to a pandemic.”
Gilead pauses access to experimental Covid-19 drug due to ‘overwhelming demand’
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