As the world scrambles to stem the rapid spread of the killer Ebola virus, the World Health Organization is hosting a meeting Monday to discuss the ethics of using experimental drugs.
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While impoverished Guinea, Liberia and Sierra Leone account for the bulk of the cases, the latest outbreak has spread further afield, with Nigeria, Africa’s most populous country, counting two deaths.
Numerous countries have imposed a raft of emergency measures, including flight bans or screening of passengers.
In the latest such move, the Ivory Coast announced Monday it was banning all flights from the three hardest-hit nations.
Ebola causes fever and, in the worst cases, unstoppable bleeding, and can be fatal in up to 90 percent of cases, according to the WHO.
The virus spreads by close contact with an infected person through bodily fluids such as sweat, blood and tissue.
The latest outbreak — which the WHO says is by far the worst since the virus was discovered four decades ago — has killed around 55-60 percent of those infected.
The WHO said Saturday that clinical trials of vaccines against Ebola should begin soon and will likely be ready for widespread use by early next year.
“I think it’s realistic,” Kieny told AFP.
ZMapp appears to have been efficient in two repatriated American aid workers and which is now being administered to an infected Catholic priest repatriated to Spain.
But there are only about a handful of available treatments, and it remains unclear how quickly production could be ramped up.
As WHO engages with pharmaceutical companies and governments to try to speed up the development process of vaccines and drugs, it is faced with a range of pressing ethical questions.
Should anyone infected with the virus be given experimental treatments? And what about those who have been exposed, or who could easily become exposed due to their work, such as health care workers?
Monday’s meeting, whose conclusions are due for release on Tuesday, will also look at how far testing must have progressed before an experimental drug can be provided, said Kieny.
“Is there a set of characteristics that these unregistered medicines should meet in terms of having demonstrated efficacy in terms of safety data, and in how many humans?”
Kieny said the session would only address the principles and provide guidance to the WHO on how to proceed, but that the UN agency planned a longer meeting later to look further into the issue.
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Đăng ký: VietNam News