FDA
approves La Jolla's low blood pressure drug
Send a link to a friend
[December 22, 2017] (Reuters)
- La Jolla Pharmaceutical said on Thursday
the U.S. Food and Drug Administration had approved its drug, Giapreza,
to treat dangerously low blood pressure.
|
The company said it plans to make Giapreza available for patients in
the United States in March.
La Jolla's shares rose 4.2 percent to $32.45 in extended trading on
Thursday.
However, the drug can cause dangerous blood clots with serious
consequences and preventive treatment for blood clots should be
used, the FDA said. http://bit.ly/2pbdgrg
The injectable works by increasing blood pressure in adults
suffering a shock, a critical condition in which blood pressure
drops so low that the brain, kidneys and other vital organs can't
receive enough blood flow to function properly.
There are about 800,000 distributive shock cases in the United
States every year, of which about 90 percent are septic shock, the
most common form of distributive shock, the company said.
[to top of second column] |
About 300,000 of these cases are not adequately treated with current
standard therapy, according to the company's estimates.
(Reporting by Tamara Mathias in Bengaluru; Editing by Sriraj
Kalluvila)
[© 2017 Thomson Reuters. All rights
reserved.] Copyright 2017 Reuters. All rights reserved. This material may not be published,
broadcast, rewritten or redistributed. |