New Trial Results Support Treatment With Inspra (eplerenone) Within First 24 Hours Of Symptoms, In Addition To Standard Therapy, In Patients With Acute STEMI Without Heart Failure.
DISCLOSURE NOTICE: The information contained in this release is as of March 10, 2013. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.
This release contains forward-looking information about a potential additional indication for Inspra, including its potential benefits, that involves substantial risks and uncertainties. Such risks and uncertainties include, among other things, the uncertainties inherent in research and development; whether and when supplemental drug applications may be filed with regulatory authorities for this potential additional indication for Inspra; decisions by regulatory authorities regarding whether and when to approve any supplemental drug applications that may be filed for this potential additional indication for Inspra as well as their decisions regarding labeling and other matters that could affect its availability or commercial potential; and competitive developments.
A further list and description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2012, and in its reports on Form 10-Q and Form 8-K.
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