Tests Of New Ebola Drugs Could Take Place As Early As November
Health officials are gearing up to test drugs and vaccines against Ebola in West Africa, and they hope to start within two months. That's an ambitious timeline for a process that often takes years. The challenge is to move forward as quickly as possible while minimizing the risks that come with unproven drugs and vaccines.
Right now there are no proven medications. But researchers have been working methodically for years on vaccines that could protect people from the Ebola virus — and drugs that could treat the sick.
"These drugs can only be tested properly during epidemics because that's the only time we have Ebola patients," says Dr. Peter Horby at the Centre for Tropical Medicine and Global Health at Oxford University.
Horby is heading a project funded by Britain's Wellcome Trust. He hopes to enroll the first patients by the end of November. "That is a very ambitious timeline by clinical trial standards, but I think that has to be our aspiration," he says.
The plan is to run these drug tests out of West African Ebola treatment clinics set up by Doctors Without Borders.
The short list of possible drugs includes ZMapp, which has been tried with a handful of patients in this outbreak, and an experimental drug made by a company called Tekmira, which was given to a medical worker with Ebola who was treated in Nebraska.
A third candidate is called AVI-7537, being developed by Sarepta Therapeutics in Cambridge, Mass. Sarepta started to develop this drug in 2010 under a contract with the U.S. military to work on drugs for Ebola and the closely related Marburg virus.
"The Ebola study got discontinued in late 2012 because of the fiscal budgetary issues in the United States at the time," says Dr. Michael Wong, senior medical director for infectious diseases at Sarepta.
Early tests showed the drug appeared safe in a small sample of people and fairly effective in treating monkeys with Ebola. But the budget cut stopped further tests.
Wong says there's enough of this potential drug for 25 patients to receive a full course of treatment, which should be sufficient for initial tests in West Africa. If those results are promising, the company has enough ingredients to make another 100 to 150 doses. But that's still a minuscule supply.
Sarepta would like to produce tens of thousands of doses in a matter of months. "That's the corporate goal," Wong says. But the company doesn't have funding to ramp up production on speculation that the drug will be effective. It's looking for funding but hasn't found it yet, Wong says.
The government is paying the company that makes Zmapp to ramp up production.
The supply lag is not such a big issue for potential vaccines. Pharmaceutical giant GlaxoSmithKline has been developing a vaccine to protect people from Ebola. It is gearing up to produce tens of thousands of doses by the end of the year, even before testing it broadly in people.
"We are doing extraordinary things to try to accelerate this development to the point where we can do something that would normally take a year to a year-and-a-half in just a few months," says Dr. Ripley Ballou of GSK Biologicals in Belgium.
If the vaccine appears to be safe, the company could start offering it to health care workers in West Africa, who have the highest risk of getting Ebola. But the potential benefit would have to outweigh the risk of unexpected problems that could result from the hurried testing.
Dr. Horby at Oxford says he still believes that public health measures — like finding and isolating people sick with Ebola — will have the biggest impact on stopping the epidemic. "But at the same time," he says, "there are other things like vaccines, like drugs, that can contribute to that, and we should be pursuing that actively as well, because this is a huge humanitarian crisis."
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Transcript
AUDIE CORNISH, HOST:
Health officials wanted to know if experimental drugs used by Americans could save other people from Ebola.
STEVE INSKEEP, HOST:
Early in west Africa's outbreak, several Americans who work there were flown home for treatment. That treatment included several experimental drugs, and the patients survived.
CORNISH: Now health officials are gearing up to test those same drugs and some experimental vaccines inside the countries worst hit by Ebola. They want to get clinical trials running within months; it's a process that usually takes years. NPR's Richard Harris reports.
RICHARD HARRIS, BYLINE: Researchers have been working methodically on vaccines that could protect people from the Ebola virus and drugs that could treat sick people. The research has been going on for many years, but Dr. Peter Horby at Oxford University says no product has made the leap from the laboratory to widespread human tests.
PETER HORBY: These drugs can only be tested properly during epidemics because that's the only time that we will have Ebola patients.
HARRIS: And with the current epidemic growing so rapidly, there's a sense of real urgency. So Horby has funding from Britain's Wellcome Trust to put at least a handful of experimental drugs to the test.
HORBY: What we would like to do is to enroll our first patients before the end of November. Now, that is a very ambitious timeline by clinical trial standards, but I think that has to be our aspiration.
HARRIS: Horby plans to run the tests at west African clinics set up by Doctors Without Borders, and he has a short list of possible drugs. It includes ZMapp, which has been tried in a handful of patients in this outbreak, and a potential drug made by a company called Tekmira, which was given to a medical worker with Ebola who was treated in Nebraska. A third candidate is called AVI-7537. Sarepta Therapeutics in Cambridge, Massachusetts, started to develop this drug in 2010 under a contract with the U.S. military.
MICHAEL WONG: The Ebola study got discontinued in late 2012 because of the fiscal budgetary issues in the United States at the time.
HARRIS: That's Dr. Michael Wong from Sarepta. Those early tests showed it appeared to be safe in a small sample of people and fairly effective in treating monkeys with Ebola, but the budget cut stopped further tests to develop the medication. And Wong says there's a little bit of that drug left over.
WONG: There's enough drug substance to treat up to 25 adult patients for a full course.
HARRIS: He says that should be enough for the initial tests in west Africa. And if those initial results are promising, the company has enough ingredients to make another 100 to 150 doses, but that's still a miniscule supply.
So could you get tens of thousands of doses in a matter of months, say?
WONG: That's the corporate goal.
HARRIS: But Wong says Sarepta is a small company that doesn't have the money to ramp up production right now just on speculation that the drug will end up working.
You'd think that some government agency would say, wow, you know, if this works, we want more yesterday, and they would be giving you money right now to ramp up your production.
WONG: Yeah, no, absolutely.
HARRIS: Sarepta is looking for that money, but it hasn't found a donor as yet. The government is paying the company that makes ZMapp to ramp up its production, and the supply lag is not such a big issue for potential vaccines. Pharmaceutical giant GlaxoSmithKline has been developing a vaccine to protect people from Ebola. Ripley Ballou from GSK Biologicals in Belgium says the company is gearing up to produce tens of thousands of doses of the vaccine even before they test it broadly in people.
RIPLEY BALLOU: We are doing extraordinary things to try to accelerate this development to the point where we can do something that would normally take us a year to a year-and-a-half in just a few months.
HARRIS: So when you say a couple of months, do you think you could have tens of thousands of doses by the end of this calendar year?
BALLOU: Well, that's our plan.
HARRIS: If the vaccine appears to be safe, they could start offering it to health care workers in west Africa since they are at highest risk of getting Ebola. The potential benefit to them would have to outweigh the risk of unexpected problems, which could result from the hurried testing. Dr. Peter Horby at Oxford says he still believes that public health measures - like finding and isolating people sick with Ebola - will have the biggest impact on stopping the epidemic.
HORBY: But at the same time, there are other things, like vaccines, like drugs, that can contribute to that. And we should be pursuing those actively as well because this is a huge humanitarian crisis.
HARRIS: The challenge is to move forward as quickly as possible while minimizing the risks that come with unproven drugs and vaccines. Richard Harris, NPR News. Transcript provided by NPR, Copyright NPR.
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