The vaccine candidates - two designed to protect against Ebola and
one against the Marburg virus - will be transferred to the Sabin
Vaccine Institute in Washington, D.C., GSK said in a statement.
There is no financial element to the agreement, a spokesman said.
The deal will see Sabin continue to develop the candidate vaccines,
one of which - a potential Ebola shot known as ChAd3 - has been
through mid-stage, Phase II, trials in Africa and could possibly be
used to halt or limit future Ebola epidemics.
"Enabling Sabin to build on the scientific progress GSK has
delivered up to Phase II increases the likelihood these candidate
vaccines may help prevent potential future outbreaks," Thomas Breuer,
chief medical officer of GSK Vaccines, said in a statement.
GSK had put its Ebola vaccine work on hold after it was unable to
progress the product through final stage, or Phase III, clinical
trials toward the end of the 2014-16 epidemic, due to a dwindling
number of Ebola cases.
An ongoing outbreak of Ebola in the Democratic Republic of Congo was
last month declared an international health emergency by the World
Health Organization (WHO).
[to top of second column] |
The disease has killed more than 1,800 people in the Congo outbreak
which began a year ago and has become the second-worst on record.
Breuer said the deal with Sabin was an "important next step" in the
fight against Ebola.
GSK said Sabin had agreed a collaboration deal with the Vaccine
Research Center at the U.S. National Institute of Allergy and
Infectious Diseases to further develop the vaccine candidates.
The ChAd3 shot was originally developed by NIAID in collaboration
with the Swiss-based firm Okairos, which was bought by GSK in 2013.
All three experimental vaccines have shown promise in safety trials
after being administered to more than 5,000 adults and 600 children,
GSK said.
(Reporting by Kate Kelland; editing by Jason Neely)
[© 2019 Thomson Reuters. All rights
reserved.] Copyright 2019 Reuters. All rights reserved. This material may not be published,
broadcast, rewritten or redistributed.
Thompson Reuters is solely responsible for this content. |