Two Experimental Ebola Drugs Reduce Mortality Rate
August 12 2019 - 3:16PM
Dow Jones News
By Gabriele Steinhauser
Two experimental Ebola drugs significantly improve a patient's
chance of surviving the virus, according to preliminary data from a
medical trial released Monday, offering fresh hope for stopping an
outbreak of the disease that has gripped parts of the Democratic
Republic of Congo for more than a year.
Of the 2,831 people who have been infected with Ebola in eastern
Congo since Aug. 1, 2018, two-thirds -- or 1,888 -- have died,
according to the World Health Organization. But patients who
received a cocktail of antibodies developed by U.S. drugmaker
Regeneron Pharmaceuticals Inc. only faced a 29% mortality rate,
said Anthony Fauci, director of the U.S. National Institute of
Allergy and Infectious Diseases, or NIAID.
A second drug, developed by the NIAID and licensed by closely
held Ridgeback Biotherapeutics, reduced the mortality rate to 34%
among the patients that received it, said Dr. Fauci. That is a
significant improvement over ZMapp, made by Mapp Biopharmaceutical
Inc., another Ebola treatment that had been tested in the waning
months of the 2014-to-2016 Ebola epidemic in West Africa, which
killed more than 11,300 people. Of the patients who received ZMapp
during the trial, 49% died.
The preliminary results of the trial, which included 681
patients who contracted Ebola during the current outbreak in Congo,
are a rare success for researchers, international health officials
and aid organizations that have struggled with militia attacks and
community distrust. Last month the WHO declared the outbreak -- the
world's second deadliest and the first in an active conflict zone
-- a global public-health emergency after Ebola was detected in
Goma, a town of two million people on the border with Rwanda.
There have been isolated cases of the virus in neighboring
Uganda, and the WHO has warned about a possible spread to Rwanda,
Burundi and civil-war-torn South Sudan.
"Today we have started a new stage" in the fight against Ebola,
said Jean-Jacques Muyembe, director-general of Congo's National
Institute for Biomedical Research and part of the team of
researchers that investigated the first known outbreak of the virus
in 1976. "We can no longer say that the Ebola virus is
incurable."
Dr. Muyembe said that the promise of a cure for Ebola should get
more patients in eastern Congo to seek treatment, which will boost
their chances of survival and reduce the risk of family members and
other contacts getting sick. Health workers have already vaccinated
191,000 people in Congo, including contacts of known patients,
doctors, nurses and burial teams.
The WHO says the vaccine, while also still experimental, is
97.5% effective.
Still, resistance to medical treatment has been one of the big
challenges during the current outbreak, where many patients either
die at home or only seek help very late. On average, patients now
wait four days after the onset of Ebola symptoms before seeking
treatment and many stay away much longer, said Dr. Michael Ryan,
executive director of the WHO's health emergencies program.
Getting help early is key for survival, even with the new drugs.
Of the patients who received Regeneron's REGN-EB3 while they still
had a low viral load, only 6% died, according to Dr. Fauci, while
those receiving the NIAID's mAb114 had an 11% mortality rate.
The superior results of REGN-EB3 prompted researchers to stop
their medical trial early. ZMapp and a fourth experimental drug
used in the trial will now be dropped from the treatment plans in
Congo, with all patients receiving either REGN-EB3 or mAb114, said
Dr. Fauci. While only 681 patients were part of the clinical trial,
many more received the experimental drugs under a
compassionate-care protocol.
Even holding a controlled medical trial during an outbreak that
has seen deadly attacks on treatment centers and health workers was
a victory for researchers, aid organizations and the doctors who
had to administer the drugs. During the West African epidemic,
disputes broke out between researchers and doctors over whether it
was ethical to have to have a placebo-controlled study in the midst
of a devastating outbreak, since it would mean giving some patients
a nonactive drug.
For this trial, researchers found a way around this dilemma by
ensuring that all patients were offered a treatment, including
ZMapp, for which there were already some positive published
data.
--Thomas M. Burton contributed to this article.
Write to Gabriele Steinhauser at
gabriele.steinhauser@wsj.com
(END) Dow Jones Newswires
August 12, 2019 15:01 ET (19:01 GMT)
Copyright (c) 2019 Dow Jones & Company, Inc.
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