
Ethical Review Set for Experimental Ebola Treatment
The World Health Organization will examine an unproven Ebola treatment that showed promise in 2 Americans infected with the virus.
The World Health Organization will examine an unproven Ebola treatment that showed promise in 2 Americans infected with the virus.
The World Health Organization (WHO) is scheduled to discuss next week the widespread use of an experimental treatment for Ebola hemorrhagic fever to mitigate the ongoing outbreak in West Africa.
The unproven drug, ZMapp, which was developed by San Diego-based Mapp Biopharmaceutical, Inc, was given to American relief workers Dr. Kent Brantly and Nancy Writebol, who became infected with the Ebola virus while working with patients in Liberia.
As WHO meets to discuss ZMapp, which is available in extremely limited quantities, a panel of medical ethicists will decide whether an untested treatment should be used in the outbreak, as well as determine who should receive the drug if it is utilized,
“We are in an unusual situation in this outbreak. We have a disease with a high fatality rate without any proven treatment or vaccine,” said WHO Assistant Director-General Marie-Paule Kieny, PhD, in a press release. "We need to ask the medical ethicists to give us guidance on what the responsible thing to do is.”
President Barack Obama said in a news conference on Wednesday that it was still too early to send ZMapp to West Africa without more clarity on the efficacy of the treatment.
"I think we have to let the science guide us. And I don't think all the information is in on whether this drug is helpful,” Obama said in a
The latest figures released by WHO on Wednesday estimated the Ebola-related death toll at more than 900, with more than 1700 suspected and confirmed cases. WHO also began a 2-day emergency meeting yesterday to decide whether to declare the West African outbreak an international crisis.
As the debate continues on the use of ZMapp,
“What we’re showing are sites of vulnerability on the surface of the virus,” said C. Daniel Murin, of TSRI, in a
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