Merck Shares Up; FDA Approves Ebola Zaire Vaccine Ervebo
December 20 2019 - 12:21PM
Dow Jones News
By Michael Dabaie
Merck & Co. Inc. (MRK) shares were up 2% to $91.63 around
midday.
The company said the U.S. Food and Drug Administration approved
Ervebo for the prevention of disease caused by Zaire ebolavirus in
individuals 18 years and older.
Merck said it is working to initiate manufacturing of licensed
doses and expects these doses to start becoming available in about
the third quarter of 2020. The company said it is working closely
with the U.S. government; World Health Organization; UNICEF; and
Gavi, the Vaccine Alliance.
Merck said that, during this transition period, it is continuing
to work with its partners to ensure uninterrupted access to the
investigational Ebola Zaire vaccine, V920, in support of ongoing
international response efforts in the Democratic Republic of the
Congo and neighboring countries.
Merck said it also made submissions to African country national
regulatory authorities in collaboration with the African Vaccine
Regulatory Forum that will allow the vaccine to be registered in
African countries considered to be at-risk for Ebola outbreaks by
the WHO.
Merck also said Friday that Keytruda received new approvals from
the Japan Pharmaceuticals and Medical Devices Agency in advanced
renal cell carcinoma and head and neck cancer for three additional
indications.
Write to Michael Dabaie at michael.dabaie@wsj.com
(END) Dow Jones Newswires
December 20, 2019 12:06 ET (17:06 GMT)
Copyright (c) 2019 Dow Jones & Company, Inc.
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