J&J's Janssen Gets FDA OK of Twice-Yearly Invega for Adults With Schizophrenia
01 Settembre 2021 - 3:00PM
Dow Jones News
By Colin Kellaher
Johnson & Johnson's Janssen Pharmaceutical Cos. unit on
Wednesday said the U.S. Food and Drug Administration approved a
six-month version of its antipsychotic Invega.
The drug maker said Invega Hafyera is the first FDA-approved
twice-yearly injectable for the treatment of schizophrenia in
adults.
Janssen said patients must first be treated with its Invega
Sustenna one-month drug for at least four months or its Invega
Trinza three-month dose at least once before switching to the new
six-month Invega Hafyera.
Write to Colin Kellaher at colin.kellaher@wsj.com
(END) Dow Jones Newswires
September 01, 2021 08:45 ET (12:45 GMT)
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