By Colin Kellaher

 

Johnson & Johnson's (JNJ) Janssen Pharmaceutical Cos. unit on Wednesday said it filed with the European Medicines Agency for expanded use of its Spravato nasal spray in adults at imminent risk for suicide.

The drug maker said it is seeking European approval for Spravato as an acute short-term treatment, co-administered with oral antidepressant therapy, for the rapid reduction of depressive symptoms in adults with a moderate-to-severe depressive episode of major depressive disorder who have current suicidal ideation with intent.

The European Commission last month approved Spravato for adults with treatment-resistant major depressive disorder.

 

Write to Colin Kellaher at colin.kellaher@wsj.com

 

(END) Dow Jones Newswires

January 15, 2020 08:10 ET (13:10 GMT)

Copyright (c) 2020 Dow Jones & Company, Inc.
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