JULY
8, 2019
FRANKFURT (Reuters) -
Bayer will apply for approval to make its blockbuster blood thinner Xarelto
available for treating children, the German company said on Monday, after a
study showed strong efficacy and safety in children with thromboembolism.
The results of the
phase III study were similar to those seen in previous studies with adults, the
German company said in a statement.
Bayer added that it
would submit an application to the European Medicines Agency for an extension
of the Xarelto marketing authorization. It did not give a time frame.
Xarelto is Bayer’s
best-selling drug and contributed 3.6 billion euros ($4.04 billion) in revenue
to the group’s pharmaceutical business last year.
Bayer jointly
developed Xarelto with Johnson & Johnson’s Janssen Pharmaceuticals, which
sells the blood clot preventer under a licensing agreement in the United
States.
J&J reported 2018
Xarelto sales of $2.47 billion.
Reporting by Patricia Weiss; Writing by Thomas Seythal; Editing
by Michelle Martin
Our Standards:The Thomson
Reuters Trust Principles.
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