LONDON -- An experimental Ebola vaccine tested on thousands of people in Guinea seems to work and might help shut down the waning epidemic in West Africa, according to interim results from a study published Friday.
There is no licensed treatment or vaccine for Ebola, which so far has killed more than 11,000 people in West Africa since the world's biggest outbreak began in the forest region of Guinea last year. Cases have dropped dramatically in recent months in the other two hard-hit countries, Sierra Leone and Liberia.
"If proven effective, this is going to be a game-changer," said Dr. Margaret Chan, director-general of the World Health Organization, which sponsored the study. "It will change the management of the current outbreak and future outbreaks."
Scientists have struggled for years to develop Ebola treatments and vaccines but have faced several hurdles, including the sporadic nature of outbreaks and funding shortages. Many past attempts have failed, including a recently abandoned drug being tested in West Africa by Tekmira Pharmaceuticals.
For the study, researchers gave one dose of the new vaccine to more than 4,000 health-care workers and other people within 10 days of their close contact with a sick Ebola patient. Another group of 3,500 people got the shot more than 10 days after their exposure to the infectious virus. In the group that received the vaccine immediately, there were no Ebola cases, versus 16 cases in people who got delayed vaccinations.
The vaccine, developed by the Canadian government, has been licensed to Merck & Co. but has not been approved by regulators yet. The study results were published online Friday in the journal Lancet.
At the moment, officials think the vaccine would be used only once an outbreak starts, to protect those at high risk; there are no plans to introduce mass vaccination campaigns like those for measles or polio or to create huge stockpiles of the shots.
Merck, based in Kenilworth, New Jersey, noted its vaccine is in what is normally the final round of human testing in Sierra Leone, and in mid-stage testing in Liberia.
Merck will manufacture the vaccine if it's approved for use outside patient studies. In Friday trading in the U.S., Merck shares were up 62 cents, or 1.1 percent, at $59.13.
In December, Gavi, the vaccine alliance, said it would spend up to $300 million buying approved Ebola vaccines.
The private-public partnership, which often buys immunizations for poor countries, said Friday it "stands ready to support the implementation of a WHO-recommended Ebola vaccine."
An expert group monitoring the study's data and safety recommended the trial be stopped July 26 so everyone exposed to Ebola in Guinea could be immunized.
The vaccine uses an Ebola protein to prompt the body's immune system to attack the virus.
"It looks to be about as safe as a flu vaccine," said Ben Neuman, a virologist at the University of Reading who was not part of the trial.
Researchers still are assessing possible side effects; the most serious seemed to be fever and the stress experienced by patients who believe such symptoms were due to Ebola.
"This (vaccine) could be the key that we've been missing to end the outbreak," Neuman said. "I don't see any reason on humanitarian grounds why it should not be used immediately."
He said further tests would be necessary to see whether the vaccine might protect pregnant women, children and adolescents. Those trials are underway.
It's uncertain how long protection might last.
AP Business Writer Linda A. Johnson in Trenton, N.J., contributed to this report.
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