WASHINGTON (AP) - The use of an experimental drug to treat two Americans diagnosed with Ebola is raising ethical questions about who gets first access to unproven new therapies for the deadly disease. But some health experts fear debate over extremely limited doses will distract from tried-and-true measures to curb the growing outbreak - things like more rapidly identifying and isolating the sick.
The World Health Organization is convening a meeting of medical ethicists next week to examine what it calls “the responsible thing to do” about whatever supplies eventually may become available of a medicine that’s never been tested in people.
At least one country involved in the outbreak is interested in the drug. Nigeria’s health minister, Onyenbuchi Chukwu, said at a news conference that he had asked the U.S. Centers for Disease Control and Prevention about access. CDC Director Tom Frieden “conveyed there are virtually no doses available” but that basic supportive care can work, a CDC spokesman said Wednesday.
President Barack Obama said Ebola is controllable and the U.S. and its allies are working to help overwhelmed public health systems in West Africa take the needed steps.
Asked about the experimental drug, Obama said all the information isn’t in: “We’ve got to let the science guide us.”
There is no proven treatment or vaccine for Ebola, which so far has infected more than 1,700 people and killed more than 930 in West Africa in what has become the worst outbreak of this viral hemorrhagic fever.
“How many times have we found magic therapies that ended up … doing more harm than good?” cautioned University of Minnesota professor Michael Osterholm, who advises the U.S. government on infectious disease threats.
“Vaccine and drug treatment right now is not going to be the main way you bring this to a stop,” he added.
Scientists stress that there’s no way to tell if the experimental drug ZMapp really made a difference for two American aid workers infected while working in Liberia.
“We don’t even know if it works,” stressed Dr. Anthony Fauci of the National Institutes of Health, which helped fund research that led to the drug’s development.
The drug is a cocktail of three antibodies engineered to recognize Ebola and bind to infected cells so that the immune system can kill them. People’s immune systems make antibodies to fight off various diseases, and attempts to cull those antibodies - from the blood of people who survive an illness, or from animals - date back to the 19th century and early diphtheria treatment. Using modern techniques to fight Ebola, scientists culled antibodies from laboratory mice, Fauci said, and ZMapp’s maker now grows the antibodies in tobacco plants and then purifies them.
Fauci said the manufacturer has told the government that it would take two to three months to produce even “a modest amount.” So the NIH is exploring ways to ramp up production, necessary to attempt formal testing or to consider more so-called compassionate use.
“Everybody’s trying to speed things up,” said Fauci, director of NIH’s National Institute of Allergy and Infectious Diseases.
To help improve diagnosis in affected countries, the Food and Drug Administration on Wednesday authorized emergency use of an experimental blood test to detect Ebola. Early symptoms - fever, vomiting and diarrhea - can be confused with other illnesses. The test was developed by the Defense Department, and is only for use in DOD-designated laboratories.
This week, the WHO is convening an emergency committee to determine if the outbreak warrants being declared a “public health emergency of international concern,” meaning it poses significant risk to other countries and requires more of an international response.