FDA approves Progenics'
treatment for rare adrenal gland tumors
Send a link to a friend
[July 31, 2018]
(Reuters) - The U.S. Food and Drug
Administration (FDA) on Monday approved Progenics Pharmaceuticals Inc's
treatment for two types of rare adrenal gland tumors, making it the
first drug approved in the United States for this use.
|
The drug, Azedra, was approved to treat patients above the age of 12
who have either of the two tumors - pheochromocytoma or
paraganglioma - and require anti-cancer therapy, the FDA said
https://bit.ly/2Ovz75p.
The two tumor types affect the adrenal gland that releases the
adrenaline hormone, which triggers the body's defense mechanism.
Pheochromocytomas increases production of some of the hormones made
in the gland, leading to high blood pressure.
[to top of second column] |
The health regulator said the drug would be used to treat patients
whose tumor has spread beyond the original site and cannot be
surgically removed.
Trading in the shares of the company were halted.
(Reporting by Manas Mishra in Bengaluru; Editing by Sai Sachin
Ravikumar)
[© 2018 Thomson Reuters. All rights
reserved.] Copyright 2018 Reuters. All rights reserved. This material may not be published,
broadcast, rewritten or redistributed.
Thompson Reuters is solely responsible for this content. |